Targeting the Checkpoint to Kill Cancer Cells
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
26295265
PubMed Central
PMC4598780
DOI
10.3390/biom5031912
PII: biom5031912
Knihovny.cz E-zdroje
- Klíčová slova
- ATM, ATR, Chk1, DNA damage response, Wee1, cancer, checkpoint, inhibitor, p53, replication stress,
- MeSH
- buněčná smrt účinky léků MeSH
- cílená molekulární terapie metody MeSH
- inhibitory proteinkinas farmakologie terapeutické užití MeSH
- kontrolní body buněčného cyklu účinky léků MeSH
- lidé MeSH
- nádorový supresorový protein p53 metabolismus MeSH
- nádory farmakoterapie enzymologie metabolismus patologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- inhibitory proteinkinas MeSH
- nádorový supresorový protein p53 MeSH
Cancer treatments such as radiotherapy and most of the chemotherapies act by damaging DNA of cancer cells. Upon DNA damage, cells stop proliferation at cell cycle checkpoints, which provides them time for DNA repair. Inhibiting the checkpoint allows entry to mitosis despite the presence of DNA damage and can lead to cell death. Importantly, as cancer cells exhibit increased levels of endogenous DNA damage due to an excessive replication stress, inhibiting the checkpoint kinases alone could act as a directed anti-cancer therapy. Here, we review the current status of inhibitors targeted towards the checkpoint effectors and discuss mechanisms of their actions in killing of cancer cells.
Zobrazit více v PubMed
Lukas J., Lukas C., Bartek J. More than just a focus: The chromatin response to DNA damage and its role in genome integrity maintenance. Nat. Cell Biol. 2011;13:1161–1169. doi: 10.1038/ncb2344. PubMed DOI
Medema R.H., Macurek L. Checkpoint control and cancer. Oncogene. 2012;31:2601–2613. doi: 10.1038/onc.2011.451. PubMed DOI
Lemaire M., Mondesert O., Bugler B., Ducommun B. Ability of human Cdc25B phosphatase splice variants to replace the function of the fission yeast Cdc25 cell cycle regulator. FEMS Yeast Res. 2004;5:205–211. doi: 10.1016/j.femsyr.2004.07.003. PubMed DOI
Manke I.A., Nguyen A., Lim D., Stewart M.Q., Elia A.E., Yaffe M.B. Mapkap kinase-2 is a cell cycle checkpoint kinase that regulates the G2/M transition and S phase progression in response to UV irradiation. Mol. Cell. 2005;17:37–48. doi: 10.1016/j.molcel.2004.11.021. PubMed DOI
Uchida S., Watanabe N., Kudo Y., Yoshioka K., Matsunaga T., Ishizaka Y., Nakagama H., Poon R.Y., Yamashita K. SCFβ(TrCP) mediates stress-activated MAPK-induced Cdc25B degradation. J. Cell Sci. 2011;124:2816–2825. doi: 10.1242/jcs.083931. PubMed DOI
Imbriano C., Gurtner A., Cocchiarella F., di Agostino S., Basile V., Gostissa M., Dobbelstein M., del Sal G., Piaggio G., Mantovani R. Direct P53 transcriptional repression: In vivo analysis of ccaat-containing G2/M promoters. Mol. Cell. Biol. 2005;25:3737–3751. doi: 10.1128/MCB.25.9.3737-3751.2005. PubMed DOI PMC
McKenzie L., King S., Marcar L., Nicol S., Dias S.S., Schumm K., Robertson P., Bourdon J.C., Perkins N., Fuller-Pace F., et al. p53-dependent repression of polo-like kinase-1 (PLK1) Cell Cycle. 2010;9:4200–4212. doi: 10.4161/cc.9.20.13532. PubMed DOI PMC
Lord C.J., Ashworth A. The DNA damage response and cancer therapy. Nature. 2012;481:287–294. doi: 10.1038/nature10760. PubMed DOI
Bouwman P., Jonkers J. Molecular pathways: How can BRCA-mutated tumors become resistant to PARP inhibitors? Clin. Cancer Res. 2014;20:540–547. doi: 10.1158/1078-0432.CCR-13-0225. PubMed DOI
Banerjee S., Kaye S.B., Ashworth A. Making the best of PARP inhibitors in ovarian cancer. Nat. Rev. Clin. Oncol. 2010;7:508–519. doi: 10.1038/nrclinonc.2010.116. PubMed DOI
Lord C.J., Ashworth A. Mechanisms of resistance to therapies targeting BRCA-mutant cancers. Nat. Med. 2013;19:1381–1388. doi: 10.1038/nm.3369. PubMed DOI
Bartkova J., Horejsi Z., Koed K., Kramer A., Tort F., Zieger K., Guldberg P., Sehested M., Nesland J.M., Lukas C., et al. DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis. Nature. 2005;434:864–870. doi: 10.1038/nature03482. PubMed DOI
Gorgoulis V.G., Vassiliou L.V., Karakaidos P., Zacharatos P., Kotsinas A., Liloglou T., Venere M., Ditullio R.A., Jr., Kastrinakis N.G., Levy B., et al. Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions. Nature. 2005;434:907–913. doi: 10.1038/nature03485. PubMed DOI
Castedo M., Perfettini J.L., Roumier T., Andreau K., Medema R., Kroemer G. Cell death by mitotic catastrophe: A molecular definition. Oncogene. 2004;23:2825–2837. doi: 10.1038/sj.onc.1207528. PubMed DOI
Zhou B.B., Bartek J. Targeting the checkpoint kinases: Chemosensitization versus chemoprotection. Nat. Rev. Cancer. 2004;4:216–225. doi: 10.1038/nrc1296. PubMed DOI
Tse A.N., Rendahl K.G., Sheikh T., Cheema H., Aardalen K., Embry M., Ma S., Moler E.J., Ni Z.J., Lopes de Menezes D.E., et al. CHIR-124, a novel potent inhibitor of Chk1, potentiates the cytotoxicity of topoisomerase I poisons in vitro and in vivo. Clin. Cancer Res. 2007;13:591–602. doi: 10.1158/1078-0432.CCR-06-1424. PubMed DOI
Blasina A., Hallin J., Chen E., Arango M.E., Kraynov E., Register J., Grant S., Ninkovic S., Chen P., Nichols T., et al. Breaching the DNA damage checkpoint via PF-00477736, a novel small-molecule inhibitor of checkpoint kinase 1. Mol. Cancer Ther. 2008;7:2394–2404. doi: 10.1158/1535-7163.MCT-07-2391. PubMed DOI
Zabludoff S.D., Deng C., Grondine M.R., Sheehy A.M., Ashwell S., Caleb B.L., Green S., Haye H.R., Horn C.L., Janetka J.W., et al. AZD7762, a novel checkpoint kinase inhibitor, drives checkpoint abrogation and potentiates DNA-targeted therapies. Mol. Cancer Ther. 2008;7:2955–2966. doi: 10.1158/1535-7163.MCT-08-0492. PubMed DOI
Guzi T.J., Paruch K., Dwyer M.P., Labroli M., Shanahan F., Davis N., Taricani L., Wiswell D., Seghezzi W., Penaflor E., et al. Targeting the replication checkpoint using SCH 900776, a potent and functionally selective Chk1 inhibitor identified via high content screening. Mol. Cancer Ther. 2011;10:591–602. doi: 10.1158/1535-7163.MCT-10-0928. PubMed DOI
Macheret M., Halazonetis T.D. DNA replication stress as a hallmark of cancer. Annu. Rev. Pathol. 2015;10:425–448. doi: 10.1146/annurev-pathol-012414-040424. PubMed DOI
Toledo L.I., Altmeyer M., Rask M.B., Lukas C., Larsen D.H., Povlsen L.K., Bekker-Jensen S., Mailand N., Bartek J., Lukas J. ATR prohibits replication catastrophe by preventing global exhaustion of RPA. Cell. 2013;155:1088–1103. doi: 10.1016/j.cell.2013.10.043. PubMed DOI
Sorensen C.S., Syljuasen R.G. Safeguarding genome integrity: The checkpoint kinases ATR, Chk1 and Wee1 restrain Cdk activity during normal DNA replication. Nucleic Acids Res. 2012;40:477–486. doi: 10.1093/nar/gkr697. PubMed DOI PMC
Petermann E., Helleday T. Pathways of mammalian replication fork restart. Nat. Rev. Mol. Cell Biol. 2010;11:683–687. doi: 10.1038/nrm2974. PubMed DOI
Fugger K., Chu W.K., Haahr P., Kousholt A.N., Beck H., Payne M.J., Hanada K., Hickson I.D., Sorensen C.S. FBH1 co-operates with MUS81 in inducing DNA double-strand breaks and cell death following replication stress. Nat. Commun. 2013 doi: 10.1038/ncomms2395. PubMed DOI
Brown E.J., Baltimore D. ATR disruption leads to chromosomal fragmentation and early embryonic lethality. Genes Dev. 2000;14:397–402. PubMed PMC
Takai H., Tominaga K., Motoyama N., Minamishima Y.A., Nagahama H., Tsukiyama T., Ikeda K., Nakayama K., Nakanishi M., Nakayama K. Aberrant cell cycle checkpoint function and early embryonic death in Chk1(−/−) mice. Genes Dev. 2000;14:1439–1447. PubMed PMC
Tominaga Y., Li C., Wang R.H., Deng C.X. Murine WEE1 plays a critical role in cell cycle regulation and pre-implantation stages of embryonic development. Int. J. Biol. Sci. 2006;2:161–170. doi: 10.7150/ijbs.2.161. PubMed DOI PMC
Montano R., Chung I., Garner K.M., Parry D., Eastman A. Preclinical development of the novel Chk1 inhibitor SCH900776 in combination with DNA-damaging agents and antimetabolites. Mol. Cancer Ther. 2012;11:427–438. doi: 10.1158/1535-7163.MCT-11-0406. PubMed DOI PMC
Brooks K., Oakes V., Edwards B., Ranall M., Leo P., Pavey S., Pinder A., Beamish H., Mukhopadhyay P., Lambie D., et al. A potent Chk1 inhibitor is selectively cytotoxic in melanomas with high levels of replicative stress. Oncogene. 2013;32:788–796. doi: 10.1038/onc.2012.72. PubMed DOI
Ferrao P.T., Bukczynska E.P., Johnstone R.W., McArthur G.A. Efficacy of Chk inhibitors as single agents in MYC-driven lymphoma cells. Oncogene. 2012;31:1661–1672. doi: 10.1038/onc.2011.358. PubMed DOI
Krajewska M., Fehrmann R.S., Schoonen P.M., Labib S., de Vries E.G., Franke L., van Vugt M.A. ATR inhibition preferentially targets homologous recombination-deficient tumor cells. Oncogene. 2015;34:3474–3481. doi: 10.1038/onc.2014.276. PubMed DOI
Mak J.P., Man W.Y., Ma H.T., Poon R.Y. Pharmacological targeting the ATR-Chk1-Wee1 axis involves balancing cell growth stimulation and apoptosis. Oncotarget. 2014;5:10546–10557. PubMed PMC
Huertas P., Cortes-Ledesma F., Sartori A.A., Aguilera A., Jackson S.P. Cdk targets SAE2 to control DNA-end resection and homologous recombination. Nature. 2008;455:689–692. doi: 10.1038/nature07215. PubMed DOI PMC
Huertas P., Jackson S.P. Human ctip mediates cell cycle control of DNA end resection and double strand break repair. J. Biol. Chem. 2009;284:9558–9565. doi: 10.1074/jbc.M808906200. PubMed DOI PMC
Sorensen C.S., Hansen L.T., Dziegielewski J., Syljuasen R.G., Lundin C., Bartek J., Helleday T. The cell-cycle checkpoint kinase Chk1 is required for mammalian homologous recombination repair. Nat. Cell Biol. 2005;7:195–201. doi: 10.1038/ncb1212. PubMed DOI
Krajewska M., Heijink A.M., Bisselink Y.J., Seinstra R.I., Sillje H.H., de Vries E.G., van Vugt M.A. Forced activation of Cdk1 via Wee1 inhibition impairs homologous recombination. Oncogene. 2013;32:3001–3008. doi: 10.1038/onc.2012.296. PubMed DOI
Thacker J. The RAD51 gene family, genetic instability and cancer. Cancer Lett. 2005;219:125–135. doi: 10.1016/j.canlet.2004.08.018. PubMed DOI
Paul A., Paul S. The breast cancer susceptibility genes (BRCA) in breast and ovarian cancers. Frontiers in bioscience. 2014;19:605–618. doi: 10.2741/4230. PubMed DOI PMC
Qiu L., Burgess A., Fairlie D.P., Leonard H., Parsons P.G., Gabrielli B.G. Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells. Mol. Biol. Cell. 2000;11:2069–2083. doi: 10.1091/mbc.11.6.2069. PubMed DOI PMC
Brooks K., Ranall M., Spoerri L., Stevenson A., Gunasingh G., Pavey S., Meunier F., Gonda T.J., Gabrielli B. Decatenation checkpoint-defective melanomas are dependent on PI3K for survival. Pigment Cell Melanoma Res. 2014;27:813–821. doi: 10.1111/pcmr.12268. PubMed DOI
Pavey S., Spoerri L., Haass N.K., Gabrielli B. DNA repair and cell cycle checkpoint defects as drivers and therapeutic targets in melanoma. Pigment Cell Melanoma Res. 2013;26:805–816. doi: 10.1111/pcmr.12136. PubMed DOI
Grenon M., Gilbert C., Lowndes N.F. Checkpoint activation in response to double-strand breaks requires the MRE11/RAD50/XRS2 complex. Nat. Cell Biol. 2001;3:844–847. doi: 10.1038/ncb0901-844. PubMed DOI
Lee J.H., Paull T.T. Activation and regulation of ATM kinase activity in response to DNA double-strand breaks. Oncogene. 2007;26:7741–7748. doi: 10.1038/sj.onc.1210872. PubMed DOI
Burma S., Chen B.P., Murphy M., Kurimasa A., Chen D.J. ATM phosphorylates histone H2AX in response to DNA double-strand breaks. J. Biol. Chem. 2001;276:42462–42467. doi: 10.1074/jbc.C100466200. PubMed DOI
Melander F., Bekker-Jensen S., Falck J., Bartek J., Mailand N., Lukas J. Phosphorylation of SDT repeats in the MDC1 N terminus triggers retention of NBS1 at the DNA damage-modified chromatin. J. Cell Biol. 2008;181:213–226. doi: 10.1083/jcb.200708210. PubMed DOI PMC
Ahn J.Y., Schwarz J.K., Piwnica-Worms H., Canman C.E. Threonine 68 phosphorylation by ataxia telangiectasia mutated is required for efficient activation of Chk2 in response to ionizing radiation. Cancer Res. 2000;60:5934–5936. PubMed
Powell S.N., DeFrank J.S., Connell P., Eogan M., Preffer F., Dombkowski D., Tang W., Friend S. Differential sensitivity of p53(−) and p53(+) cells to caffeine-induced radiosensitization and override of G2 delay. Cancer Res. 1995;55:1643–1648. doi: 10.1016/0360-3016(95)97825-L. PubMed DOI
Price B.D., Youmell M.B. The phosphatidylinositol 3-kinase inhibitor wortmannin sensitizes murine fibroblasts and human tumor cells to radiation and blocks induction of p53 following DNA damage. Cancer Res. 1996;56:246–250. PubMed
Hickson I., Zhao Y., Richardson C.J., Green S.J., Martin N.M., Orr A.I., Reaper P.M., Jackson S.P., Curtin N.J., Smith G.C. Identification and characterization of a novel and specific inhibitor of the ataxia-telangiectasia mutated kinase ATM. Cancer Res. 2004;64:9152–9159. doi: 10.1158/0008-5472.CAN-04-2727. PubMed DOI
Rainey M.D., Charlton M.E., Stanton R.V., Kastan M.B. Transient inhibition of ATM kinase is sufficient to enhance cellular sensitivity to ionizing radiation. Cancer Res. 2008;68:7466–7474. doi: 10.1158/0008-5472.CAN-08-0763. PubMed DOI PMC
Golding S.E., Rosenberg E., Valerie N., Hussaini I., Frigerio M., Cockcroft X.F., Chong W.Y., Hummersone M., Rigoreau L., Menear K.A., et al. Improved ATM kinase inhibitor KU-60019 radiosensitizes glioma cells, compromises insulin, AKT and ERK prosurvival signaling, and inhibits migration and invasion. Mol. Cancer Ther. 2009;8:2894–2902. doi: 10.1158/1535-7163.MCT-09-0519. PubMed DOI PMC
Batey M.A., Zhao Y., Kyle S., Richardson C., Slade A., Martin N.M., Lau A., Newell D.R., Curtin N.J. Preclinical evaluation of a novel ATM inhibitor, KU59403, in vitro and in vivo in p53 functional and dysfunctional models of human cancer. Mol. Cancer Ther. 2013;12:959–967. doi: 10.1158/1535-7163.MCT-12-0707. PubMed DOI PMC
Raso A., Vecchio D., Cappelli E., Ropolo M., Poggi A., Nozza P., Biassoni R., Mascelli S., Capra V., Kalfas F., et al. Characterization of glioma stem cells through multiple stem cell markers and their specific sensitization to double-strand break-inducing agents by pharmacological inhibition of ataxia telangiectasia mutated protein. Brain Pathol. 2012;22:677–688. doi: 10.1111/j.1750-3639.2012.00566.x. PubMed DOI PMC
Golding S.E., Rosenberg E., Adams B.R., Wignarajah S., Beckta J.M., O’Connor M.J., Valerie K. Dynamic inhibition of ATM kinase provides a strategy for glioblastoma multiforme radiosensitization and growth control. Cell Cycle. 2012;11:1167–1173. doi: 10.4161/cc.11.6.19576. PubMed DOI PMC
Vecchio D., Daga A., Carra E., Marubbi D., Baio G., Neumaier C.E., Vagge S., Corvo R., Brisigotti M.P., Ravetti J.L., et al. Predictability, efficacy and safety of radiosensitization of glioblastoma-initiating cells by the ATM inhibitor KU-60019. Int. J. Cancer. 2014;135:479–491. doi: 10.1002/ijc.28680. PubMed DOI
Biddlestone-Thorpe L., Sajjad M., Rosenberg E., Beckta J.M., Valerie N.C., Tokarz M., Adams B.R., Wagner A.F., Khalil A., Gilfor D., et al. Atm kinase inhibition preferentially sensitizes p53-mutant glioma to ionizing radiation. Clin. Cancer Res. 2013;19:3189–3200. doi: 10.1158/1078-0432.CCR-12-3408. PubMed DOI PMC
Hoeijmakers J.H. Genome maintenance mechanisms for preventing cancer. Nature. 2001;411:366–374. doi: 10.1038/35077232. PubMed DOI
Jazayeri A., Falck J., Lukas C., Bartek J., Smith G.C., Lukas J., Jackson S.P. ATM- and cell cycle-dependent regulation of ATR in response to DNA double-strand breaks. Nat. Cell Biol. 2006;8:37–45. doi: 10.1038/ncb1337. PubMed DOI
Sartori A.A., Lukas C., Coates J., Mistrik M., Fu S., Bartek J., Baer R., Lukas J., Jackson S.P. Human ctip promotes DNA end resection. Nature. 2007;450:509–514. doi: 10.1038/nature06337. PubMed DOI PMC
Kousholt A.N., Fugger K., Hoffmann S., Larsen B.D., Menzel T., Sartori A.A., Sorensen C.S. CtIP-dependent DNA resection is required for DNA damage checkpoint maintenance but not initiation. J. Cell Biol. 2012;197:869–876. doi: 10.1083/jcb.201111065. PubMed DOI PMC
Wold M.S. Replication protein a: A heterotrimeric, single-stranded DNA-binding protein required for eukaryotic DNA metabolism. Annu. Rev. Biochem. 1997;66:61–92. doi: 10.1146/annurev.biochem.66.1.61. PubMed DOI
Cortez D., Guntuku S., Qin J., Elledge S.J. ATR and ATRIP: Partners in checkpoint signaling. Science. 2001;294:1713–1716. doi: 10.1126/science.1065521. PubMed DOI
Cotta-Ramusino C., McDonald E.R., 3rd, Hurov K., Sowa M.E., Harper J.W., Elledge S.J. A DNA damage response screen identifies RHINO, a 9-1-1 and TopBP1 interacting protein required for ATR signaling. Science. 2011;332:1313–1317. doi: 10.1126/science.1203430. PubMed DOI PMC
Kumagai A., Lee J., Yoo H.Y., Dunphy W.G. TopBP1 activates the ATR-ATRIP complex. Cell. 2006;124:943–955. doi: 10.1016/j.cell.2005.12.041. PubMed DOI
Delacroix S., Wagner J.M., Kobayashi M., Yamamoto K., Karnitz L.M. The Rad9-Hus1-Rad1 (9-1-1) clamp activates checkpoint signaling via TopBP1. Genes Dev. 2007;21:1472–1477. doi: 10.1101/gad.1547007. PubMed DOI PMC
Lee J., Kumagai A., Dunphy W.G. The Rad9-Hus1-Rad1 checkpoint clamp regulates interaction of TopBP1 with ATR. J. Biol. Chem. 2007;282:28036–28044. doi: 10.1074/jbc.M704635200. PubMed DOI
Wang J., Gong Z., Chen J. MDC1 collaborates with TopBP1 in DNA replication checkpoint control. J. Cell Biol. 2011;193:267–273. doi: 10.1083/jcb.201010026. PubMed DOI PMC
Jeong S.Y., Kumagai A., Lee J., Dunphy W.G. Phosphorylated claspin interacts with a phosphate-binding site in the kinase domain of Chk1 during ATR-mediated activation. J. Biol. Chem. 2003;278:46782–46788. doi: 10.1074/jbc.M304551200. PubMed DOI
Kumagai A., Dunphy W.G. Repeated phosphopeptide motifs in claspin mediate the regulated binding of Chk1. Nat. Cell Biol. 2003;5:161–165. doi: 10.1038/ncb921. PubMed DOI
Liu Q., Guntuku S., Cui X.S., Matsuoka S., Cortez D., Tamai K., Luo G., Carattini-Rivera S., DeMayo F., Bradley A., et al. Chk1 is an essential kinase that is regulated by ATR and required for the G2/M DNA damage checkpoint. Genes Dev. 2000;14:1448–1459. PubMed PMC
Gilad O., Nabet B.Y., Ragland R.L., Schoppy D.W., Smith K.D., Durham A.C., Brown E.J. Combining ATR suppression with oncogenic Ras synergistically increases genomic instability, causing synthetic lethality or tumorigenesis in a dosage-dependent manner. Cancer Res. 2010;70:9693–9702. doi: 10.1158/0008-5472.CAN-10-2286. PubMed DOI PMC
Murga M., Campaner S., Lopez-Contreras A.J., Toledo L.I., Soria R., Montaña M.F., D’Artista L., Schleker T., Guerra C., Garcia E., et al. Exploiting oncogene-induced replicative stress for the selective killing of MYC-driven tumors. Nat. Struct. Mol. Biol. 2011;18:1331–1335. doi: 10.1038/nsmb.2189. PubMed DOI PMC
Schoppy D.W., Ragland R.L., Gilad O., Shastri N., Peters A.A., Murga M., Fernandez-Capetillo O., Diehl J.A., Brown E.J. Oncogenic stress sensitizes murine cancers to hypomorphic suppression of ATR. J. Clin. Investig. 2012;122:241–252. doi: 10.1172/JCI58928. PubMed DOI PMC
Flynn R.L., Cox K.E., Jeitany M., Wakimoto H., Bryll A.R., Ganem N.J., Bersani F., Pineda J.R., Suvà M.L., Benes C.H., et al. Alternative lengthening of telomeres renders cancer cells hypersensitive to ATR inhibitors. Science. 2015;347:273–277. doi: 10.1126/science.1257216. PubMed DOI PMC
Mohni K.N., Thompson P.S., Luzwick J.W., Glick G.G., Pendleton C.S., Lehmann B.D., Pietenpol J.A., Cortez D. A synthetic lethal screen identifies DNA repair pathways that sensitize cancer cells to combined ATR inhibition and cisplatin treatments. PLoS ONE. 2015;10:e0125482. doi: 10.1371/journal.pone.0125482. PubMed DOI PMC
Sultana R., Abdel-Fatah T., Perry C., Moseley P., Albarakti N., Mohan V., Seedhouse C., Chan S., Madhusudan S. Ataxia telangiectasia mutated and RAD3 related (ATR) protein kinase inhibition is synthetically lethal in XRCC1 deficient ovarian cancer cells. PLoS ONE. 2013;8:e57098. doi: 10.1371/journal.pone.0057098. PubMed DOI PMC
Charrier J.D., Durrant S.J., Golec J.M., Kay D.P., Knegtel R.M., MacCormick S., Mortimore M., O’Donnell M.E., Pinder J.L., Reaper P.M., et al. Discovery of potent and selective inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents. J. Med. Chem. 2011;54:2320–2330. doi: 10.1021/jm101488z. PubMed DOI
Reaper P.M., Griffiths M.R., Long J.M., Charrier J.D., Maccormick S., Charlton P.A., Golec J.M., Pollard J.R. Selective killing of ATM- or p53-deficient cancer cells through inhibition of ATR. Nat. Chem. Biol. 2011;7:428–430. doi: 10.1038/nchembio.573. PubMed DOI
Prevo R., Fokas E., Reaper P.M., Charlton P.A., Pollard J.R., McKenna W.G., Muschel R.J., Brunner T.B. The novel ATR inhibitor VE-821 increases sensitivity of pancreatic cancer cells to radiation and chemotherapy. Cancer Biol. Ther. 2012;13:1072–1081. doi: 10.4161/cbt.21093. PubMed DOI PMC
Huntoon C.J., Flatten K.S., Wahner Hendrickson A.E., Huehls A.M., Sutor S.L., Kaufmann S.H., Karnitz L.M. Atr inhibition broadly sensitizes ovarian cancer cells to chemotherapy independent of BRCA status. Cancer Res. 2013;73:3683–3691. doi: 10.1158/0008-5472.CAN-13-0110. PubMed DOI PMC
Vavrova J., Zarybnicka L., Lukasova E., Rezacova M., Novotna E., Sinkorova Z., Tichy A., Pejchal J., Durisova K. Inhibition of ATR kinase with the selective inhibitor VE-821 results in radiosensitization of cells of promyelocytic leukaemia (HL-60) Radiat. Environ. Biophys. 2013;52:471–479. doi: 10.1007/s00411-013-0486-5. PubMed DOI
Salovska B., Fabrik I., Durisova K., Link M., Vavrova J., Rezacova M., Tichy A. Radiosensitization of human leukemic HL-60 cells by ATR kinase inhibitor (VE-821): Phosphoproteomic analysis. Int. J. Mol. Sci. 2014;15:12007–12026. doi: 10.3390/ijms150712007. PubMed DOI PMC
Abdel-Fatah T.M., Middleton F.K., Arora A., Agarwal D., Chen T., Moseley P.M., Perry C., Doherty R., Chan S., Green A.R., et al. Untangling the ATR-CHEK1 network for prognostication, prediction and therapeutic target validation in breast cancer. Mol. Oncol. 2015;9:569–585. doi: 10.1016/j.molonc.2014.10.013. PubMed DOI PMC
Fokas E., Prevo R., Pollard J.R., Reaper P.M., Charlton P.A., Cornelissen B., Vallis K.A., Hammond E.M., Olcina M.M., Gillies McKenna W., et al. Targeting atr in vivo using the novel inhibitor VE-822 results in selective sensitization of pancreatic tumors to radiation. Cell Death Dis. 2012;3:e441. doi: 10.1038/cddis.2012.181. PubMed DOI PMC
Hall A.B., Newsome D., Wang Y., Boucher D.M., Eustace B., Gu Y., Hare B., Johnson M.A., Milton S., Murphy C.E., et al. Potentiation of tumor responses to DNA damaging therapy by the selective ATR inhibitor VX-970. Oncotarget. 2014;5:5674–5685. PubMed PMC
Foote K.M., Blades K., Cronin A., Fillery S., Guichard S.S., Hassall L., Hickson I., Jacq X., Jewsbury P.J., McGuire T.M., et al. Discovery of 4-{4-[(3R)-3-Methylmorpholin-4-yl]-6-[1-(methylsulfonyl)cyclopropyl]pyrimidin-2-yl}-1H-indole (AZ20): A potent and selective inhibitor of ATR protein kinase with monotherapy in vivo antitumor activity. J. Med. Chem. 2013;56:2125–2138. doi: 10.1021/jm301859s. PubMed DOI
Guichard S.M., Brown E., Odedra R., Hughes A., Heathcote D., Barnes J., Lau A., Powell S., Jones C.D., Nissink W., et al. The pre-clinical in vitro and in vivo activity of AZD6738: A potent and selective inhibitor of ATR kinase. Cancer Res. 2013 doi: 10.1158/1538-7445.AM2013-3343. DOI
Liu Y., Vidanes G., Lin Y.C., Mori S., Siede W. Characterization of a Saccharomyces cerevisiae homologue of Schizosaccharomyces pombe Chk1 involved in DNA-damage-induced M-phase arrest. Mol. Gen. Genet. 2000;262:1132–1146. doi: 10.1007/PL00008656. PubMed DOI
Okita N., Minato S., Ohmi E., Tanuma S., Higami Y. DNA damage-induced Chk1 autophosphorylation at Ser296 is regulated by an intramolecular mechanism. FEBS Lett. 2012;586:3974–3979. doi: 10.1016/j.febslet.2012.09.048. PubMed DOI
Kasahara K., Goto H., Enomoto M., Tomono Y., Kiyono T., Inagaki M. 14-3-3gamma mediates Cdc25A proteolysis to block premature mitotic entry after DNA damage. EMBO J. 2010;29:2802–2812. doi: 10.1038/emboj.2010.157. PubMed DOI PMC
Busino L., Donzelli M., Chiesa M., Guardavaccaro D., Ganoth D., Dorrello N.V., Hershko A., Pagano M., Draetta G.F. Degradation of Cdc25A by beta-TRCP during S phase and in response to DNA damage. Nature. 2003;426:87–91. doi: 10.1038/nature02082. PubMed DOI
Jin J., Shirogane T., Xu L., Nalepa G., Qin J., Elledge S.J., Harper J.W. Scfbeta-TRCP links Chk1 signaling to degradation of the Cdc25A protein phosphatase. Genes Dev. 2003;17:3062–3074. doi: 10.1101/gad.1157503. PubMed DOI PMC
Forrest A., Gabrielli B. Cdc25B activity is regulated by 14-3-3. Oncogene. 2001;20:4393–4401. doi: 10.1038/sj.onc.1204574. PubMed DOI
Graves P.R., Lovly C.M., Uy G.L., Piwnica-Worms H. Localization of human Cdc25C is regulated both by nuclear export and 14-3-3 protein binding. Oncogene. 2001;20:1839–1851. doi: 10.1038/sj.onc.1204259. PubMed DOI
Schwarz J.K., Lovly C.M., Piwnica-Worms H. Regulation of the Chk2 protein kinase by oligomerization-mediated cis- and trans-phosphorylation. Mol. Cancer Res. 2003;1:598–609. PubMed
Jack M.T., Woo R.A., Hirao A., Cheung A., Mak T.W., Lee P.W. Chk2 is dispensable for p53-mediated G1 arrest but is required for a latent p53-mediated apoptotic response. Proc. Natl. Acad. Sci. USA. 2002;99:9825–9829. doi: 10.1073/pnas.152053599. PubMed DOI PMC
Ma C.X., Janetka J.W., Piwnica-Worms H. Death by releasing the breaks: Chk1 inhibitors as cancer therapeutics. Trends Mol. Med. 2011;17:88–96. doi: 10.1016/j.molmed.2010.10.009. PubMed DOI PMC
Reinhardt H.C., Aslanian A.S., Lees J.A., Yaffe M.B. p53-deficient cells rely on ATM- and ATR-mediated checkpoint signaling through the p38MAPK/MK2 pathway for survival after DNA damage. Cancer Cell. 2007;11:175–189. doi: 10.1016/j.ccr.2006.11.024. PubMed DOI PMC
Bunch R.T., Eastman A. Enhancement of cisplatin-induced cytotoxicity by 7-hydroxystaurosporine (UCN-01), a new G2-checkpoint inhibitor. Clin. Cancer Res. 1996;2:791–797. PubMed
Tse A.N., Schwartz G.K. Potentiation of cytotoxicity of topoisomerase i poison by concurrent and sequential treatment with the checkpoint inhibitor UCN-01 involves disparate mechanisms resulting in either p53-independent clonogenic suppression or p53-dependent mitotic catastrophe. Cancer Res. 2004;64:6635–6644. doi: 10.1158/0008-5472.CAN-04-0841. PubMed DOI
Fuse E., Tanii H., Kurata N., Kobayashi H., Shimada Y., Tamura T., Sasaki Y., Tanigawara Y., Lush R.D., Headlee D., et al. Unpredicted clinical pharmacology of UCN-01 caused by specific binding to human alpha1-acid glycoprotein. Cancer Res. 1998;58:3248–3253. PubMed
Kortmansky J., Shah M.A., Kaubisch A., Weyerbacher A., Yi S., Tong W., Sowers R., Gonen M., O’Reilly E., Kemeny N., et al. Phase I trial of the cyclin-dependent kinase inhibitor and protein kinase C inhibitor 7-hydroxystaurosporine in combination with fluorouracil in patients with advanced solid tumors. J. Clin. Oncol. 2005;23:1875–1884. doi: 10.1200/JCO.2005.03.116. PubMed DOI
Dent P., Tang Y., Yacoub A., Dai Y., Fisher P.B., Grant S. Chk1 inhibitors in combination chemotherapy: Thinking beyond the cell cycle. Mol. Interv. 2011;11:133–140. doi: 10.1124/mi.11.2.11. PubMed DOI PMC
Matthews D.J., Yakes F.M., Chen J., Tadano M., Bornheim L., Clary D.O., Tai A., Wagner J.M., Miller N., Kim Y.D., et al. Pharmacological abrogation of S-phase checkpoint enhances the anti-tumor activity of gemcitabine in vivo. Cell Cycle. 2007;6:104–110. doi: 10.4161/cc.6.1.3699. PubMed DOI
Sausville E., Lorusso P., Carducci M., Carter J., Quinn M.F., Malburg L., Azad N., Cosgrove D., Knight R., Barker P., et al. Phase I dose-escalation study of AZD7762, a checkpoint kinase inhibitor, in combination with gemcitabine in US patients with advanced solid tumors. Cancer Chemother. Pharmacol. 2014;73:539–549. doi: 10.1007/s00280-014-2380-5. PubMed DOI PMC
Weiss G.J., Donehower R.C., Iyengar T., Ramanathan R.K., Lewandowski K., Westin E., Hurt K., Hynes S.M., Anthony S.P., McKane S. Phase I dose-escalation study to examine the safety and tolerability of ly2603618, a checkpoint 1 kinase inhibitor, administered 1 day after pemetrexed 500 mg/m2 every 21 days in patients with cancer. Investig. New Drug. 2013;31:136–144. doi: 10.1007/s10637-012-9815-9. PubMed DOI PMC
King C., Diaz H., Barnard D., Barda D., Clawson D., Blosser W., Cox K., Guo S., Marshall M. Characterization and preclinical development of ly2603618: A selective and potent Chk1 inhibitor. Investig. New Drugs. 2014;32:213–226. doi: 10.1007/s10637-013-0036-7. PubMed DOI
Calvo E., Chen V., Marshall M., Ohnmacht U., Hynes S., Kumm E., Diaz H.B., Barnard D., Merzoug F., Huber L., et al. Preclinical analyses and phase I evaluation of ly2603618 administered in combination with pemetrexed and cisplatin in patients with advanced cancer. Investig. New Drug. 2014;32:955–968. doi: 10.1007/s10637-014-0114-5. PubMed DOI
Daud A.I., Ashworth M.T., Strosberg J., Goldman J.W., Mendelson D., Springett G., Venook A.P., Loechner S., Rosen L.S., Shanahan F., et al. Phase I dose-escalation trial of checkpoint kinase 1 inhibitor MK-8776 as monotherapy and in combination with gemcitabine in patients with advanced solid tumors. J. Clin. Oncol. 2015;33:1060–1066. doi: 10.1200/JCO.2014.57.5027. PubMed DOI
Watanabe N., Broome M., Hunter T. Regulation of the human WEE1HU Cdk tyrosine 15-kinase during the cell cycle. EMBO J. 1995;14:1878–1891. PubMed PMC
Watanabe N., Arai H., Nishihara Y., Taniguchi M., Watanabe N., Hunter T., Osada H. M-phase kinases induce phospho-dependent ubiquitination of somatic Wee1 by SCFβ-TrCP. Proc. Natl. Acad. Sci. USA. 2004;101:4419–4424. doi: 10.1073/pnas.0307700101. PubMed DOI PMC
Lee J., Kumagai A., Dunphy W.G. Positive regulation of Wee1 by Chk1 and 14-3-3 proteins. Mol. Biol. Cell. 2001;12:551–563. doi: 10.1091/mbc.12.3.551. PubMed DOI PMC
Parker L.L., Piwnica-Worms H. Inactivation of the p34Cdc2-cyclin B complex by the human Wee1 tyrosine kinase. Science. 1992;257:1955–1957. doi: 10.1126/science.1384126. PubMed DOI
Saini P., Li Y., Dobbelstein M. Wee1 is required to sustain ATR/Chk1 signaling upon replicative stress. Oncotarget. 2015;6:13072–13087. PubMed PMC
Panek R.L., Lu G.H., Klutchko S.R., Batley B.L., Dahring T.K., Hamby J.M., Hallak H., Doherty A.M., Keiser J.A. In vitro pharmacological characterization of PD 166285, a new nanomolar potent and broadly active protein tyrosine kinase inhibitor. J. Pharmacol. Exp. Ther. 1997;283:1433–1444. PubMed
Wang Y., Li J., Booher R.N., Kraker A., Lawrence T., Leopold W.R., Sun Y. Radiosensitization of p53 mutant cells by PD0166285, a novel G(2) checkpoint abrogator. Cancer Res. 2001;61:8211–8217. PubMed
Palmer B.D., Thompson A.M., Booth R.J., Dobrusin E.M., Kraker A.J., Lee H.H., Lunney E.A., Mitchell L.H., Ortwine D.F., Smaill J.B., et al. 4-Phenylpyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione inhibitors of the checkpoint kinase Wee1. Structure-activity relationships for chromophore modification and phenyl ring substitution. J. Med. Chem. 2006;49:4896–4911. doi: 10.1021/jm0512591. PubMed DOI
Arora S., Bisanz K.M., Peralta L.A., Basu G.D., Choudhary A., Tibes R., Azorsa D.O. RNAi screening of the kinome identifies modulators of cisplatin response in ovarian cancer cells. Gynecol. Oncol. 2010;118:220–227. doi: 10.1016/j.ygyno.2010.05.006. PubMed DOI
Hirai H., Iwasawa Y., Okada M., Arai T., Nishibata T., Kobayashi M., Kimura T., Kaneko N., Ohtani J., Yamanaka K., et al. Small-molecule inhibition of Wee1 kinase by MK-1775 selectively sensitizes p53-deficient tumor cells to DNA-damaging agents. Mol. Cancer Ther. 2009;8:2992–3000. doi: 10.1158/1535-7163.MCT-09-0463. PubMed DOI
Mizuarai S., Yamanaka K., Itadani H., Arai T., Nishibata T., Hirai H., Kotani H. Discovery of gene expression-based pharmacodynamic biomarker for a p53 context-specific anti-tumor drug Wee1 inhibitor. Mol. Cancer. 2009;8:34. doi: 10.1186/1476-4598-8-34. PubMed DOI PMC
Hirai H., Arai T., Okada M., Nishibata T., Kobayashi M., Sakai N., Imagaki K., Ohtani J., Sakai T., Yoshizumi T., et al. MK-1775, a small molecule Wee1 inhibitor, enhances anti-tumor efficacy of various DNA-damaging agents, including 5-fluorouracil. Cancer Biol Ther. 2010;9:514–522. doi: 10.4161/cbt.9.7.11115. PubMed DOI
Bridges K.A., Hirai H., Buser C.A., Brooks C., Liu H., Buchholz T.A., Molkentine J.M., Mason K.A., Meyn R.E. MK-1775, a novel Wee1 kinase inhibitor, radiosensitizes p53-defective human tumor cells. Clin. Cancer Res. 2011;17:5638–5648. doi: 10.1158/1078-0432.CCR-11-0650. PubMed DOI PMC
Rajeshkumar N.V., de Oliveira E., Ottenhof N., Watters J., Brooks D., Demuth T., Shumway S.D., Mizuarai S., Hirai H., Maitra A., et al. MK-1775, a potent Wee1 inhibitor, synergizes with gemcitabine to achieve tumor regressions, selectively in p53-deficient pancreatic cancer xenografts. Clin. Cancer Res. 2011;17:2799–2806. doi: 10.1158/1078-0432.CCR-10-2580. PubMed DOI PMC
Do K., Wilsker D., Ji J., Zlott J., Freshwater T., Kinders R.J., Collins J., Chen A.P., Doroshow J.H., Kummar S. Phase I study of single-agent AZD1775 (MK-1775), a Wee1 kinase inhibitor, in patients with refractory solid tumors. J. Clin. Oncol. 2015 doi: 10.1200/JCO.2014.60.4009. PubMed DOI PMC
Carrassa L., Chila R., Lupi M., Ricci F., Celenza C., Mazzoletti M., Broggini M., Damia G. Combined inhibition of chk1 and wee1: In vitro synergistic effect translates to tumor growth inhibition in vivo. Cell Cycle. 2012;11:2507–2517. doi: 10.4161/cc.20899. PubMed DOI
Russell M.R., Levin K., Rader J., Belcastro L., Li Y., Martinez D., Pawel B., Shumway S.D., Maris J.M., Cole K.A. Combination therapy targeting the Chk1 and Wee1 kinases shows therapeutic efficacy in neuroblastoma. Cancer Res. 2013;73:776–784. doi: 10.1158/0008-5472.CAN-12-2669. PubMed DOI PMC
Chila R., Basana A., Lupi M., Guffanti F., Gaudio E., Rinaldi A., Cascione L., Restelli V., Tarantelli C., Bertoni F., et al. Combined inhibition of Chk1 and Wee1 as a new therapeutic strategy for mantle cell lymphoma. Oncotarget. 2015;6:3394–3408. PubMed PMC
Magnussen G.I., Emilsen E., Giller Fleten K., Engesaeter B., Nahse-Kumpf V., Fjaer R., Slipicevic A., Florenes V.A. Combined inhibition of the cell cycle related proteins Wee1 and Chk1/2 induces synergistic anti-cancer effect in melanoma. BMC Cancer. 2015 doi: 10.1186/s12885-015-1474-8. PubMed DOI PMC
Raman M., Earnest S., Zhang K., Zhao Y., Cobb M.H. TAO kinases mediate activation of p38 in response to DNA damage. EMBO J. 2007;26:2005–2014. doi: 10.1038/sj.emboj.7601668. PubMed DOI PMC
Brancho D., Tanaka N., Jaeschke A., Ventura J.J., Kelkar N., Tanaka Y., Kyuuma M., Takeshita T., Flavell R.A., Davis R.J. Mechanism of p38 MAP kinase activation in vivo. Genes Dev. 2003;17:1969–1978. doi: 10.1101/gad.1107303. PubMed DOI PMC
Ben-Levy R., Leighton I.A., Doza Y.N., Attwood P., Morrice N., Marshall C.J., Cohen P. Identification of novel phosphorylation sites required for activation of MAPKAP kinase-2. EMBO J. 1995;14:5920–5930. PubMed PMC
Reinhardt H.C., Hasskamp P., Schmedding I., Morandell S., van Vugt M.A., Wang X., Linding R., Ong S.E., Weaver D., Carr S.A., et al. DNA damage activates a spatially distinct late cytoplasmic cell-cycle checkpoint network controlled by MK2-mediated RNA stabilization. Mol. Cell. 2010;40:34–49. doi: 10.1016/j.molcel.2010.09.018. PubMed DOI PMC
Morandell S., Reinhardt H.C., Cannell I.G., Kim J.S., Ruf D.M., Mitra T., Couvillon A.D., Jacks T., Yaffe M.B. A reversible gene-targeting strategy identifies synthetic lethal interactions between MK2 and p53 in the DNA damage response in vivo. Cell Rep. 2013;5:868–877. doi: 10.1016/j.celrep.2013.10.025. PubMed DOI PMC
Dietlein F., Kalb B., Jokic M., Noll E.M., Strong A., Tharun L., Ozretic L., Kunstlinger H., Kambartel K., Randerath W.J., et al. A synergistic interaction between Chk1- and MK2 inhibitors in KRAS-mutant cancer. Cell. 2015;162:146–159. doi: 10.1016/j.cell.2015.05.053. PubMed DOI
Petitjean A., Achatz M.I., Borresen-Dale A.L., Hainaut P., Olivier M. Tp53 mutations in human cancers: Functional selection and impact on cancer prognosis and outcomes. Oncogene. 2007;26:2157–2165. doi: 10.1038/sj.onc.1210302. PubMed DOI
Ventura A., Kirsch D.G., McLaughlin M.E., Tuveson D.A., Grimm J., Lintault L., Newman J., Reczek E.E., Weissleder R., Jacks T. Restoration of p53 function leads to tumour regression in vivo. Nature. 2007;445:661–665. doi: 10.1038/nature05541. PubMed DOI
Khoo K.H., Verma C.S., Lane D.P. Drugging the p53 pathway: Understanding the route to clinical efficacy. Nat. Rev. Drug Discov. 2014;13:217–236. doi: 10.1038/nrd4288. PubMed DOI
Vassilev L.T., Vu B.T., Graves B., Carvajal D., Podlaski F., Filipovic Z., Kong N., Kammlott U., Lukacs C., Klein C., et al. In vivo activation of the p53 pathway by small-molecule antagonists of MDM2. Science. 2004;303:844–848. doi: 10.1126/science.1092472. PubMed DOI
Chen L., Rousseau R.F., Middleton S.A., Nichols G.L., Newell D.R., Lunec J., Tweddle D.A. Pre-clinical evaluation of the MDM2-p53 antagonist RG7388 alone and in combination with chemotherapy in neuroblastoma. Oncotarget. 2015;6:10207–10221. PubMed PMC
Ding Q., Zhang Z., Liu J.J., Jiang N., Zhang J., Ross T.M., Chu X.J., Bartkovitz D., Podlaski F., Janson C., et al. Discovery of RG7388, a potent and selective p53-MDM2 inhibitor in clinical development. J. Med. Chem. 2013;56:5979–5983. doi: 10.1021/jm400487c. PubMed DOI
Higgins B., Glenn K., Walz A., Tovar C., Filipovic Z., Hussain S., Lee E., Kolinsky K., Tannu S., Adames V., et al. Preclinical optimization of MDM2 antagonist scheduling for cancer treatment by using a model-based approach. Clin. Cancer Res. 2014;20:3742–3752. doi: 10.1158/1078-0432.CCR-14-0460. PubMed DOI
Bulavin D.V., Phillips C., Nannenga B., Timofeev O., Donehower L.A., Anderson C.W., Appella E., Fornace A.J., Jr. Inactivation of the Wip1 phosphatase inhibits mammary tumorigenesis through p38 MAPK-mediated activation of the p16(INK4A)-p19(ARF) pathway. Nat. Genet. 2004;36:343–350. doi: 10.1038/ng1317. PubMed DOI
Demidov O.N., Timofeev O., Lwin H.N., Kek C., Appella E., Bulavin D.V. Wip1 phosphatase regulates p53-dependent apoptosis of stem cells and tumorigenesis in the mouse intestine. Cell Stem Cell. 2007;1:180–190. doi: 10.1016/j.stem.2007.05.020. PubMed DOI
Saito-Ohara F., Imoto I., Inoue J., Hosoi H., Nakagawara A., Sugimoto T., Inazawa J. PPM1D is a potential target for 17q gain in neuroblastoma. Cancer Res. 2003;63:1876–1883. PubMed
Wang P., Rao J., Yang H., Zhao H., Yang L. Ppm1d silencing by lentiviral-mediated RNA interference inhibits proliferation and invasion of human glioma cells. J. Huazhong Univ. Sci. Technol. 2011;31:94–99. doi: 10.1007/s11596-011-0157-1. PubMed DOI
Gilmartin A.G., Faitg T.H., Richter M., Groy A., Seefeld M.A., Darcy M.G., Peng X., Federowicz K., Yang J., Zhang S.Y., et al. Allosteric Wip1 phosphatase inhibition through flap-subdomain interaction. Nat. Chem. Biol. 2014;10:181–187. doi: 10.1038/nchembio.1427. PubMed DOI
Richter M., Dayaram T., Gilmartin A.G., Ganji G., Pemmasani S.K., van der Key H., Shohet J.M., Donehower L.A., Kumar R. Wip1 phosphatase as a potential therapeutic target in neuroblastoma. PLoS One. 2015;10:e0115635. doi: 10.1371/journal.pone.0115635. PubMed DOI PMC
Emelyanov A., Bulavin D.V. Wip1 phosphatase in breast cancer. Oncogene. 2014 doi: 10.1038/onc.2014.375. PubMed DOI
Kleiblova P., Shaltiel I.A., Benada J., Sevcik J., Pechackova S., Pohlreich P., Voest E.E., Dundr P., Bartek J., Kleibl Z., et al. Gain-of-function mutations of Ppm1d/Wip1 impair the p53-dependent g1 checkpoint. J. Cell Biol. 2013;201:511–521. doi: 10.1083/jcb.201210031. PubMed DOI PMC
Lapenna S., Giordano A. Cell cycle kinases as therapeutic targets for cancer. Nat. Rev. Drug Discov. 2009;8:547–566. doi: 10.1038/nrd2907. PubMed DOI
Malumbres M., Barbacid M. Cell cycle, Cdks and cancer: A changing paradigm. Nat. Rev. Cancer. 2009;9:153–166. doi: 10.1038/nrc2602. PubMed DOI
Yu Q., Geng Y., Sicinski P. Specific protection against breast cancers by cyclin D1 ablation. Nature. 2001;411:1017–1021. doi: 10.1038/35082500. PubMed DOI
Landis M.W., Pawlyk B.S., Li T., Sicinski P., Hinds P.W. Cyclin D1-dependent kinase activity in murine development and mammary tumorigenesis. Cancer Cell. 2006;9:13–22. doi: 10.1016/j.ccr.2005.12.019. PubMed DOI
Puyol M., Martin A., Dubus P., Mulero F., Pizcueta P., Khan G., Guerra C., Santamaria D., Barbacid M. A synthetic lethal interaction between K-Ras oncogenes and Cdk4 unveils a therapeutic strategy for non-small cell lung carcinoma. Cancer Cell. 2010;18:63–73. doi: 10.1016/j.ccr.2010.05.025. PubMed DOI
Sicinska E., Aifantis I., Le Cam L., Swat W., Borowski C., Yu Q., Ferrando A.A., Levin S.D., Geng Y., von Boehmer H., et al. Requirement for cyclin D3 in lymphocyte development and T cell leukemias. Cancer Cell. 2003;4:451–461. doi: 10.1016/S1535-6108(03)00301-5. PubMed DOI
Schmitz R., Young R.M., Ceribelli M., Jhavar S., Xiao W., Zhang M., Wright G., Shaffer A.L., Hodson D.J., Buras E., et al. Burkitt lymphoma pathogenesis and therapeutic targets from structural and functional genomics. Nature. 2012;490:116–120. doi: 10.1038/nature11378. PubMed DOI PMC
Monahan K.B., Rozenberg G.I., Krishnamurthy J., Johnson S.M., Liu W., Bradford M.K., Horner J., Depinho R.A., Sharpless N.E. Somatic p16(Ink4A) loss accelerates melanomagenesis. Oncogene. 2010;29:5809–5817. doi: 10.1038/onc.2010.314. PubMed DOI PMC
Curtin J.A., Fridlyand J., Kageshita T., Patel H.N., Busam K.J., Kutzner H., Cho K.H., Aiba S., Brocker E.B., LeBoit P.E., et al. Distinct sets of genetic alterations in melanoma. N. Engl. J. Med. 2005;353:2135–2147. doi: 10.1056/NEJMoa050092. PubMed DOI
Smalley K.S., Lioni M., Dalla Palma M., Xiao M., Desai B., Egyhazi S., Hansson J., Wu H., King A.J., van Belle P., et al. Increased cyclin D1 expression can mediate BRAF inhibitor resistance in BRAF V600E-mutated melanomas. Mol. Cancer Ther. 2008;7:2876–2883. doi: 10.1158/1535-7163.MCT-08-0431. PubMed DOI PMC
Arguello F., Alexander M., Sterry J.A., Tudor G., Smith E.M., Kalavar N.T., Greene J.F., Jr., Koss W., Morgan C.D., Stinson S.F., et al. Flavopiridol induces apoptosis of normal lymphoid cells, causes immunosuppression, and has potent antitumor activity in vivo against human leukemia and lymphoma xenografts. Blood. 1998;91:2482–2490. PubMed
Parker B.W., Kaur G., Nieves-Neira W., Taimi M., Kohlhagen G., Shimizu T., Losiewicz M.D., Pommier Y., Sausville E.A., Senderowicz A.M. Early induction of apoptosis in hematopoietic cell lines after exposure to flavopiridol. Blood. 1998;91:458–465. PubMed
Joshi K.S., Rathos M.J., Joshi R.D., Sivakumar M., Mascarenhas M., Kamble S., Lal B., Sharma S. In vitro antitumor properties of a novel cyclin-dependent kinase inhibitor, p276–00. Mol. Cancer Ther. 2007;6:918–925. doi: 10.1158/1535-7163.MCT-06-0613. PubMed DOI
Finn R.S., Dering J., Conklin D., Kalous O., Cohen D.J., Desai A.J., Ginther C., Atefi M., Chen I., Fowst C., et al. PD 0332991, a selective cyclin D kinase 4/6 inhibitor, preferentially inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro. Breast Cancer Res. 2009 doi: 10.1186/bcr2419. PubMed DOI PMC
Choi Y.J., Li X., Hydbring P., Sanda T., Stefano J., Christie A.L., Signoretti S., Look A.T., Kung A.L., von Boehmer H., et al. The requirement for cyclin D function in tumor maintenance. Cancer Cell. 2012;22:438–451. doi: 10.1016/j.ccr.2012.09.015. PubMed DOI PMC
Sawai C.M., Freund J., Oh P., Ndiaye-Lobry D., Bretz J.C., Strikoudis A., Genesca L., Trimarchi T., Kelliher M.A., Clark M., et al. Therapeutic targeting of the cyclin D3:Cdk4/6 complex in T cell leukemia. Cancer Cell. 2012;22:452–465. doi: 10.1016/j.ccr.2012.09.016. PubMed DOI PMC
Leonard J.P., LaCasce A.S., Smith M.R., Noy A., Chirieac L.R., Rodig S.J., Yu J.Q., Vallabhajosula S., Schoder H., English P., et al. Selective Cdk4/6 inhibition with tumor responses by PD0332991 in patients with mantle cell lymphoma. Blood. 2012;119:4597–4607. doi: 10.1182/blood-2011-10-388298. PubMed DOI
Murphy C.G., Dickler M.N. The role of Cdk4/6 inhibition in breast cancer. Oncologist. 2015;20:483–490. doi: 10.1634/theoncologist.2014-0443. PubMed DOI PMC
Anders L., Ke N., Hydbring P., Choi Y.J., Widlund H.R., Chick J.M., Zhai H., Vidal M., Gygi S.P., Braun P., et al. A systematic screen for Cdk4/6 substrates links foxm1 phosphorylation to senescence suppression in cancer cells. Cancer Cell. 2011;20:620–634. doi: 10.1016/j.ccr.2011.10.001. PubMed DOI PMC
Yadav V., Chen S.H., Yue Y.G., Buchanan S., Beckmann R.P., Peng S.B. Co-targeting BRAF and cyclin dependent kinases 4/6 for BRAF mutant cancers. Pharmacol. Ther. 2015;149:139–149. doi: 10.1016/j.pharmthera.2014.12.003. PubMed DOI
Derenzini E., Agostinelli C., Imbrogno E., Iacobucci I., Casadei B., Brighenti E., Righi S., Fuligni F., di Rora A.G.L., Ferrari A., et al. Constitutive activation of the DNA damage response pathway as a novel therapeutic target in diffuse large B-cell lymphoma. Oncotarget. 2015;6:6553–6569. PubMed PMC
CHEK2 Germline Variants in Cancer Predisposition: Stalemate Rather than Checkmate
Effect of Sepatronium Bromide (YM-155) on DNA Double-Strand Breaks Repair in Cancer Cells