ZEB1/miR-200c/AGR2: A New Regulatory Loop Modulating the Epithelial-Mesenchymal Transition in Lung Adenocarcinomas

. 2020 Jun 18 ; 12 (6) : . [epub] 20200618

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid32570918

Grantová podpora
GACR 19-02014S Grantová Agentura České Republiky
MMCI, 00209805 Ministerstvo Zdravotnictví Ceské Republiky

Epithelial-mesenchymal transition (EMT) is a process involved not only in morphogenesis and embryonic development, but also in cancer progression, whereby tumor cells obtain a more aggressive metastatic phenotype. Anterior gradient protein 2 (AGR2) maintains the epithelial phenotype and blocks the induction of EMT, thus playing an undeniable role in tumor progression. However, the mechanism through which AGR2 expression is regulated, not only during EMT, but also in the early stages of cancer development, remains to be elucidated. In the present study, we show an inverse correlation of AGR2 with ZEB1 (zinc finger enhancer binding protein, δEF1) that was verified by analysis of several independent clinical data sets of lung adenocarcinomas. We also identified the ZEB1 binding site within the AGR2 promoter region and confirmed AGR2 as a novel molecular target of ZEB1. The overexpression of ZEB1 decreased the promoter activity of the AGR2 gene, which resulted in reduced AGR2 protein level and the acquisition of a more invasive phenotype of these lung cancer cells. Conversely, silencing of ZEB1 led not only to increased levels of AGR2 protein, but also attenuated the invasiveness of tumor cells. The AGR2 knockout, vice versa, increased ZEB1 expression, indicating that the ZEB1/AGR2 regulatory axis may function in a double negative feedback loop. In conclusion, we revealed for the first time that ZEB1 regulates AGR2 at the transcriptional level, while AGR2 presence contributes to ZEB1 mRNA degradation. Thus, our data identify a new regulatory mechanism between AGR2 and ZEB1, two rivals in the EMT process, tightly associated with the development of metastasis.

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Kroger C., Afeyan A., Mraz J., Eaton E.N., Reinhardt F., Khodor Y.L., Thiru P., Bierie B., Ye X., Burge C.B., et al. Acquisition of a hybrid E/M state is essential for tumorigenicity of basal breast cancer cells. Proc. Natl. Acad. Sci. USA. 2019;116:7353–7362. doi: 10.1073/pnas.1812876116. PubMed DOI PMC

Nieto M.A., Huang R.Y., Jackson R.A., Thiery J.P. Emt: 2016. Cell. 2016;166:21–45. doi: 10.1016/j.cell.2016.06.028. PubMed DOI

Pastushenko I., Brisebarre A., Sifrim A., Fioramonti M., Revenco T., Boumahdi S., Van Keymeulen A., Brown D., Moers V., Lemaire S., et al. Identification of the tumour transition states occurring during EMT. Nature. 2018;556:463–468. doi: 10.1038/s41586-018-0040-3. PubMed DOI

Batlle E., Sancho E., Franci C., Dominguez D., Monfar M., Baulida J., De Herreros A.G. The transcription factor snail is a repressor of E-cadherin gene expression in epithelial tumour cells. Nat. Cell Biol. 2000;2:84–89. doi: 10.1038/35000034. PubMed DOI

Eger A., Aigner K., Sonderegger S., Dampier B., Oehler S., Schreiber M., Berx G., Cano A., Beug H., Foisner R. DeltaEF1 is a transcriptional repressor of E-cadherin and regulates epithelial plasticity in breast cancer cells. Oncogene. 2005;24:2375–2385. doi: 10.1038/sj.onc.1208429. PubMed DOI

Lamouille S., Xu J., Derynck R. Molecular mechanisms of epithelial–mesenchymal transition. Nat. Rev. Mol. Cell Boil. 2014;15:178–196. doi: 10.1038/nrm3758. PubMed DOI PMC

Peinado H., Olmeda D., Cano A. Snail, Zeb and bHLH factors in tumour progression: An alliance against the epithelial phenotype? Nat. Rev. Cancer. 2007;7:415–428. doi: 10.1038/nrc2131. PubMed DOI

Postigo A.A., Depp J.L., Taylor J.J., Kroll K.L. Regulation of Smad signaling through a differential recruitment of coactivators and corepressors by ZEB proteins. EMBO J. 2003;22:2453–2462. doi: 10.1093/emboj/cdg226. PubMed DOI PMC

Barrallo-Gimeno A., Nieto M.A. The Snail genes as inducers of cell movement and survival: Implications in development and cancer. Development. 2005;132:3151–3161. doi: 10.1242/dev.01907. PubMed DOI

Krebs A.M., Mitschke J., Losada M.L., Schmalhofer O., Boerries M., Busch H., Böttcher M., Mougiakakos D., Reichardt W., Bronsert P., et al. The EMT-activator Zeb1 is a key factor for cell plasticity and promotes metastasis in pancreatic cancer. Nat. Cell Biol. 2017;19:518–529. doi: 10.1038/ncb3513. PubMed DOI

Sánchez-Tilló E., Siles L., De Barrios O., Cuatrecasas M., Vaquero E.C., Castells A., Postigo A. Expanding roles of ZEB factors in tumorigenesis and tumor progression. Am. J. Cancer Res. 2011;1:897–912. PubMed PMC

Zhang P., Sun Y., Ma L. ZEB1: At the crossroads of epithelial-mesenchymal transition, metastasis and therapy resistance. Cell Cycle. 2015;14:481–487. doi: 10.1080/15384101.2015.1006048. PubMed DOI PMC

Aberger F., Weidinger G., Grunz H., Richter K. Anterior specification of embryonic ectoderm: The role of the Xenopus cement gland-specific gene XAG-2. Mech. Dev. 1998;72:115–130. doi: 10.1016/S0925-4773(98)00021-5. PubMed DOI

Brychtova V., Vojtesek B., Hrstka R. Anterior gradient 2: A novel player in tumor cell biology. Cancer Lett. 2011;304:1–7. doi: 10.1016/j.canlet.2010.12.023. PubMed DOI

Hrstka R., Podhorec J., Nenutil R., Sommerova L., Obacz J., Durech M., Faktor J., Bouchal P., Skoupilova H., Vojtesek B. Tamoxifen-Dependent Induction ofAGR2Is Associated with Increased Aggressiveness of Endometrial Cancer Cells. Cancer Investig. 2017;35:313–324. doi: 10.1080/07357907.2017.1309546. PubMed DOI

Xue X., Fei X., Hou W., Zhang Y., Liu L., Hu R. miR-342-3p suppresses cell proliferation and migration by targeting AGR2 in non-small cell lung cancer. Cancer Lett. 2018;412:170–178. doi: 10.1016/j.canlet.2017.10.024. PubMed DOI

Zhang Y., Xia F., Zhang F., Cui Y., Wang Q., Liu H., Wu Y. miR-135b-5p enhances doxorubicin-sensitivity of breast cancer cells through targeting anterior gradient 2. J. Exp. Clin. Cancer Res. 2019;38:26. doi: 10.1186/s13046-019-1024-3. PubMed DOI PMC

Matoulkova E., Sommerova L., Pastorek M., Vojtesek B., Hrstka R. Regulation of AGR2 expression via 3’UTR shortening. Exp. Cell Res. 2017;356:40–47. doi: 10.1016/j.yexcr.2017.04.011. PubMed DOI

Higa A., Mulot A., Delom F., Bouchecareilh M., Nguyên D.T., Boismenu D., Wise M.J., Chevet E. Role of Pro-oncogenic Protein Disulfide Isomerase (PDI) Family Member Anterior Gradient 2 (AGR2) in the Control of Endoplasmic Reticulum Homeostasis. J. Boil. Chem. 2011;286:44855–44868. doi: 10.1074/jbc.M111.275529. PubMed DOI PMC

Obacz J., Takacova M., Brychtova V., Dobes P., Pastorekova S., Vojtesek B., Hrstka R. The role of AGR2 and AGR3 in cancer: Similar but not identical. Eur. J. Cell Boil. 2015;94:139–147. doi: 10.1016/j.ejcb.2015.01.002. PubMed DOI

Alavi M., Mah V., Maresh E.L., Bagryanova L., Horvath S., Chia D., Goodglick L., Liu A.Y. High expression of AGR2 in lung cancer is predictive of poor survival. BMC Cancer. 2015;15:655. doi: 10.1186/s12885-015-1658-2. PubMed DOI PMC

Milewski D., Balli D., Ustiyan V., Le T., Dienemann H., Warth A., Breuhahn K., Whitsett J.A., Kalinichenko V.V., Kalin T.V. FOXM1 activates AGR2 and causes progression of lung adenomas into invasive mucinous adenocarcinomas. PLoS Genet. 2017;13:e1007097. doi: 10.1371/journal.pgen.1007097. PubMed DOI PMC

Tian S.-B., Tao K.-X., Hu J., Liu Z.-B., Ding X.-L., Chu Y.-N., Cui J.-Y., Shuai X.-M., Gao J.-B., Cai K.-L., et al. The prognostic value of AGR2 expression in solid tumours: A systematic review and meta-analysis. Sci. Rep. 2017;7:15500. doi: 10.1038/s41598-017-15757-z. PubMed DOI PMC

Sommerova L., Ondrouskova E., Vojtesek B., Hrstka R. Suppression of AGR2 in a TGF-β-induced Smad regulatory pathway mediates epithelial-mesenchymal transition. BMC Cancer. 2017;17:546. doi: 10.1186/s12885-017-3537-5. PubMed DOI PMC

Fritzsche F.R., Dahl E., Dankof A., Burkhardt M., Pahl S., Petersen I., Dietel M., Kristiansen G. Expression of AGR2 in non small cell lung cancer. Histol. Histopathol. 2007;22:703–708. PubMed

Cerami E., Gao J., Dogrusoz U., Gross B.E., Sumer S.O., Aksoy B.A., Skanderup A.J., Byrne C.J., Heuer M.L., Larsson E., et al. The cBio cancer genomics portal: An open platform for exploring multidimensional cancer genomics data. Cancer Discov. 2012;2:401–404. doi: 10.1158/2159-8290.CD-12-0095. PubMed DOI PMC

Gao J., Aksoy B.A., Dogrusoz U., Dresdner G., Gross B., Sumer S.O., Sun Y., Skanderup A.J., Sinha R., Larsson E., et al. Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal. Sci. Signal. 2013;6:pl1. doi: 10.1126/scisignal.2004088. PubMed DOI PMC

Barretina J., Caponigro G., Stransky N., Venkatesan K., Margolin A.A., Kim S., Wilson C.J., Lehár J., Kryukov G., Sonkin D., et al. The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity. Nature. 2012;483:603–607. doi: 10.1038/nature11003. PubMed DOI PMC

Rhodes D.R., Yu J., Shanker K., Deshpande N., Varambally R., Ghosh D., Barrette T., Pander A., Chinnaiyan A.M. ONCOMINE: A Cancer Microarray Database and Integrated Data-Mining Platform. Neoplasia. 2004;6:1–6. doi: 10.1016/S1476-5586(04)80047-2. PubMed DOI PMC

Cline M., Craft B., Swatloski T., Goldman M., Ma S., Haussler D., Zhu J. Exploring TCGA Pan-Cancer Data at the UCSC Cancer Genomics Browser. Sci. Rep. 2013;3:2652. doi: 10.1038/srep02652. PubMed DOI PMC

Khan A., Fornes O., Stigliani A., Gheorghe M., Castro-Mondragon J.A., Van Der Lee R., Bessy A., Chèneby J., Kulkarni S.R., Tan G., et al. JASPAR 2018: Update of the open-access database of transcription factor binding profiles and its web framework. Nucleic Acids Res. 2018;46:D1284. doi: 10.1093/nar/gkx1188. PubMed DOI PMC

Dreos R., Ambrosini G., Périer R.C., Bucher P. The Eukaryotic Promoter Database: Expansion of EPDnew and new promoter analysis tools. Nucleic Acids Res. 2014;43:D92–D96. doi: 10.1093/nar/gku1111. PubMed DOI PMC

Hrstka R., Nenutil R., Fourtouna A., Maslon M.M., Naughton C., Langdon S., Murray E., Larionov A., Petrakova K., Muller P., et al. The pro-metastatic protein anterior gradient-2 predicts poor prognosis in tamoxifen-treated breast cancers. Oncogene. 2010;29:4838–4847. doi: 10.1038/onc.2010.228. PubMed DOI

Burk U., Schubert J., Wellner U., Schmalhofer O., Vincan E., Spaderna S., Brabletz T. A reciprocal repression between ZEB1 and members of the miR-200 family promotes EMT and invasion in cancer cells. EMBO Rep. 2008;9:582–589. doi: 10.1038/embor.2008.74. PubMed DOI PMC

Zhang L., Yang F., Yuan J.H., Yuan S.X., Zhou W.P., Huo X.S., Xu D., Bi H.S., Wang F., Sun S.H. Epigenetic activation of the MiR-200 family contributes to H19-mediated metastasis suppression in hepatocellular carcinoma. Carcinogenesis. 2012;34:577–586. doi: 10.1093/carcin/bgs381. PubMed DOI

Mizuguchi Y., Specht S., Lunz J.G., Isse K., Corbitt N., Takizawa T., Demetris A.J. Cooperation of p300 and PCAF in the Control of MicroRNA 200c/141 Transcription and Epithelial Characteristics. PLoS ONE. 2012;7:e32449. doi: 10.1371/journal.pone.0032449. PubMed DOI PMC

Obrdlik A., Kukalev A., Louvet E., Farrants A.K., Caputo L., Percipalle P. The Histone Acetyltransferase PCAF Associates with Actin and hnRNP U for RNA Polymerase II Transcription. Mol. Cell. Boil. 2008;28:6342–6357. doi: 10.1128/MCB.00766-08. PubMed DOI PMC

Zhang T., Guo L., Creighton C.J., Lu Q., Gibbons N.L., Yi E.S., Deng B., Molina J.R., Sun Z., Yang P., et al. A genetic cell context-dependent role for ZEB1 in lung cancer. Nat. Commun. 2016;7:12231. doi: 10.1038/ncomms12231. PubMed DOI PMC

Thiery J.P., Acloque H., Huang R.Y.-J., Nieto M.A. Epithelial-Mesenchymal Transitions in Development and Disease. Cell. 2009;139:871–890. doi: 10.1016/j.cell.2009.11.007. PubMed DOI

Fessart D., Domblides C., Avril T., Eriksson L.A., Begueret H., Pineau R., Malrieux C., Dugot-Senant N., Lucchesi C., Chevet E., et al. Secretion of protein disulphide isomerase AGR2 confers tumorigenic properties. eLife. 2016;5 doi: 10.7554/eLife.13887. PubMed DOI PMC

Heerboth S., Housman G., Leary M., Longacre M., Byler S., Lapinska K., Willbanks A., Sarkar S. EMT and tumor metastasis. Clin. Transl. Med. 2015;4:6. doi: 10.1186/s40169-015-0048-3. PubMed DOI PMC

Santos G.D.C., Shepherd F.A., Tsao M.-S. EGFR Mutations and Lung Cancer. Annu. Rev. Pathol. Mech. Dis. 2011;6:49–69. doi: 10.1146/annurev-pathol-011110-130206. PubMed DOI

Mayo C., Bertran-Alamillo J., Molina-Vila M., Gimenez-Capitan A., Costa C., Rosell R. Pharmacogenetics ofEGFRin lung cancer: Perspectives and clinical applications. Pharmacogenomics. 2012;13:789–802. doi: 10.2217/pgs.12.54. PubMed DOI

Narumi S., Miki Y., Hata S., Ebina M., Saito M., Mori K., Kobayashi M., Suzuki T., Iwabuchi E., Sato I., et al. Anterior Gradient 2 is Correlated with EGFR Mutation in Lung Adenocarcinoma Tissues. Int. J. Boil. Markers. 2015;30:234–242. doi: 10.5301/jbm.5000131. PubMed DOI

Larsen J., Nathan V., Osborne J.K., Farrow R.K., Deb D., Sullivan J.P., Dospoy P.D., Augustyn A., Hight S.K., Sato M., et al. ZEB1 drives epithelial-to-mesenchymal transition in lung cancer. J. Clin. Investig. 2016;126:3219–3235. doi: 10.1172/JCI76725. PubMed DOI PMC

Jung S.Y., Yun J., Kim S.J., Kang S., Kim D.Y., Kim Y.J., Park J.H., Jang W.B., Ji S.T., Ha J.S., et al. Basic helix-loop-helix transcription factor Twist1 is a novel regulator of anterior gradient protein 2 homolog (AGR2) in breast cancer. Biochem. Biophys. Res. Commun. 2019;516:149–156. doi: 10.1016/j.bbrc.2019.05.191. PubMed DOI

Wright T.M., Wardell S.E., Jasper J.S., Stice J.P., Safi R., Nelson E.R., McDonnell D.P. Delineation of a FOXA1/ERα/AGR2 regulatory loop that is dysregulated in endocrine therapy-resistant breast cancer. Mol. Cancer Res. 2014;12:1829–1839. doi: 10.1158/1541-7786.MCR-14-0195. PubMed DOI PMC

Vesuna F., Bergman Y., Raman V. Genomic pathways modulated by Twist in breast cancer. BMC Cancer. 2017;17:52. doi: 10.1186/s12885-016-3033-3. PubMed DOI PMC

Langer E.M., Kendsersky N.D., Daniel C.J., Kuziel G.M., Pelz C., Murphy K.M., Capecchi M.R., Sears R.C. ZEB1-repressed microRNAs inhibit autocrine signaling that promotes vascular mimicry of breast cancer cells. Oncogene. 2017;37:1005–1019. doi: 10.1038/onc.2017.356. PubMed DOI PMC

Park S.-M., Gaur A.B., Lengyel E., Peter M.E. The miR-200 family determines the epithelial phenotype of cancer cells by targeting the E-cadherin repressors ZEB1 and ZEB2. Genome Res. 2008;22:894–907. doi: 10.1101/gad.1640608. PubMed DOI PMC

Brabletz S., Brabletz T. The ZEB/miR-200 feedback loop—A motor of cellular plasticity in development and cancer? EMBO Rep. 2010;11:670–677. doi: 10.1038/embor.2010.117. PubMed DOI PMC

Title A.C., Hong S.-J., Pires N.D., Hasenöhrl L., Godbersen S., Stokar-Regenscheit N., Bartel D.P., Stoffel M. Genetic dissection of the miR-200–Zeb1 axis reveals its importance in tumor differentiation and invasion. Nat. Commun. 2018;9:4671. doi: 10.1038/s41467-018-07130-z. PubMed DOI PMC

Ljepoja B., García-Román J., Sommer A.-K., Fröhlich T., Arnold G.J., Wagner E., Roidl A. A proteomic analysis of an in vitro knock-out of miR-200c. Sci. Rep. 2018;8:6927. doi: 10.1038/s41598-018-25240-y. PubMed DOI PMC

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