Overexpression of MRP1/ABCC1, Survivin and BCRP/ABCC2 Predicts the Resistance of Diffuse Large B-Cell Lymphoma to R-CHOP Treatment
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
PubMed
37627134
PubMed Central
PMC10452886
DOI
10.3390/cancers15164106
PII: cancers15164106
Knihovny.cz E-zdroje
- Klíčová slova
- BCRP/ABCC2, MRP1/ABCC1, multidrug resistance, non-Hodgkin lymphoma, survivin,
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Approximately 40% of patients with diffuse large B-cell lymphoma (DLBCL) experience treatment resistance to the first-line R-CHOP regimen. ATP binding cassette (ABC) transporters and survivin might play a role in multidrug resistance (MDR) in various tumors. The aim was to investigate if the coexpression of ABC transporters and survivin was associated with R-CHOP treatment response. METHODS: The expression of Bcl-2, survivin, P-glycoprotein/ABCB1, MRP1/ABCC1, and BCRP/ABCC2 was analyzed using immunohistochemistry in tumor specimens obtained from patients with DLBCL, and classified according to the treatment response as Remission, Relapsed, and (primary) Refractory groups. All patients received R-CHOP or equivalent treatment. RESULTS: Bcl-2 was in strong positive correlation with clinical parameters and all biomarkers except P-gp/ABCB1. The overexpression of MRP1/ABCC1, survivin, and BCRP/ABCC2 presented as high immunoreactive scores (IRSs) was detected in the Refractory and Relapsed groups (p < 0.05 vs. Remission), respectively, whereas the IRS of P-gp/ABCB1 was low. Significant correlations were found among either MRP1/ABCC1 and survivin or BCRP/ABCC2 in the Refractory and Relapsed groups, respectively. In multiple linear regression analysis, ECOG status along with MRP1/ABCC1 or survivin and BRCP/ABCG2 was significantly associated with the prediction of the R-CHOP treatment response. CONCLUSIONS: DLBCL might harbor certain molecular signatures such as MRP1/ABCC1, survivin, and BCRP/ABCC2 overexpression that can predict resistance to R-CHOP.
Clinic of Hematology University Clinical Center of Serbia 2 Pasterova 11000 Belgrade Serbia
Department of Hematology Faculty of Medicine University of Belgrade 11000 Belgrade Serbia
Special Police Unit Ministry of Interior Trebevićka 12 A 11030 Belgrade Serbia
Zobrazit více v PubMed
He M.Y., Kridel R. Treatment resistance in diffuse large B-cell lymphoma. Leukemia. 2021;35:2151–2165. doi: 10.1038/s41375-021-01285-3. PubMed DOI
Thandra K.C., Barsouk A., Saginala K., Padala S.A., Barsouk A., Rawla P. Epidemiology of Non-Hodgkin’s Lymphoma. Med. Sci. 2021;9:5. doi: 10.3390/medsci9010005. PubMed DOI PMC
Schmitz R., Wright G.W., Huang D.W., Johnson C.A., Phelan J.D., Wang J.Q., Roulland S., Kasbekar M., Young R.M., Shaffer A.L., et al. Genetics and Pathogenesis of Diffuse Large B-Cell Lymphoma. N. Engl. J. Med. 2018;378:1396–1407. doi: 10.1056/NEJMoa1801445. PubMed DOI PMC
Choueiry F., Singh S., Sircar A., Laliotis G., Sun X., Chavdoula E., Zhang S., Helmig-Mason J., Hart A., Epperla N., et al. Integration of Metabolomics and Gene Expression Profiling Elucidates IL4I1 as Modulator of Ibrutinib Resistance in ABC-Diffuse Large B Cell Lymphoma. Cancers. 2021;13:2146. doi: 10.3390/cancers13092146. PubMed DOI PMC
Salles G., Barrett M., Foà R., Maurer J., O’Brien S., Valente N., Wenger M., Maloney D.G. Rituximab in B-Cell Hematologic Malignancies: A Review of 20 Years of Clinical Experience. Adv. Ther. 2017;34:2232–2273. doi: 10.1007/s12325-017-0612-x. PubMed DOI PMC
Pfreundschuh M., Kuhnt E., Trümper L., Osterborg A., Trneny M., Shepherd L., Gill D.S., Walewski J., Pettengell R., Jaeger U., et al. CHOP-like chemotherapy with or without rituximab in young patients with good-prognosis diffuse large-Bcell lymphoma: 6-year results of an open-label randomised study of the MabThera International Trial (MInT) Group. Lancet Oncol. 2011;12:1013–1022. doi: 10.1016/S1470-2045(11)70235-2. PubMed DOI
Lenz G. Insights into the Molecular Pathogenesis of Activated B-Cell-like Diffuse Large B-Cell Lymphoma and Its Therapeutic Implications. Cancers. 2015;7:811–822. doi: 10.3390/cancers7020812. PubMed DOI PMC
Wang L., Li L.R. R-CHOP resistance in diffuse large B-cell lymphoma: Biological and molecular mechanisms. Chin. Med. J. 2020;134:253–260. doi: 10.1097/CM9.0000000000001294. PubMed DOI PMC
Rovira J., Valera A., Colomo L., Setoain X., Rodríguez S., Martínez-Trillos A., Giné E., Dlouhy I., Magnano L., Gaya A., et al. Prognosis of Patients with Diffuse Large B Cell Lymphoma Not Reaching Complete Response or Relapsing after Frontline Chemotherapy or Immunochemotherapy. Ann. Hematol. 2015;94:803–812. doi: 10.1007/s00277-014-2271-1. PubMed DOI PMC
Crump M., Neelapu S.S., Farooq U., Van Den Neste E., Kuruvilla J., Westin J., Link B.K., Hay A., Cerhan J.R., Zhu L., et al. Outcomes in Refractory Diffuse Large B-Cell Lymphoma: Results from the International SCHOLAR-1 Study. Blood. 2017;130:1800–1808. doi: 10.1182/blood-2017-03-769620. PubMed DOI PMC
Berendsen M.R., Stevens W.B.C., van den Brand M., van Krieken J.H., Scheijen B. Molecular Genetics of Relapsed Diffuse Large B-Cell Lymphoma: Insight into Mechanisms of Therapy Resistance. Cancers. 2020;12:3553. doi: 10.3390/cancers12123553. PubMed DOI PMC
Pi M., Kuang H., Yue C., Yang Q., Wu A., Li Y., Assaraf Y.G., Yang D.H., Wu S. Targeting metabolism to overcome cancer drug resistance: A promising therapeutic strategy for diffuse large B cell lymphoma. Drug Resist. Updat. 2022;61:100822. doi: 10.1016/j.drup.2022.100822. PubMed DOI
Zhang J., Gu Y., Chen B. Drug-Resistance Mechanism and New Targeted Drugs and Treatments of Relapse and Refractory DLBCL. Cancer Manag. Res. 2023;15:245–255. doi: 10.2147/CMAR.S400013. PubMed DOI PMC
Kathawala R.J., Gupta P., Ashby C.R., Chen Z.-S. The modulation of ABC transporter-mediated multidrug resistance in cancer: A review of the past decade. Drug Resist. Updat. 2015;18:1–17. doi: 10.1016/j.drup.2014.11.002. PubMed DOI
Singh R.R., Kunkalla K., Qu C., Schlette E., Neelapu S.S., Samaniego F., Vega F. ABCG2 is a direct transcriptional target of hedgehog signaling and involved in stroma-induced drug tolerance in diffuse large B-cell lymphoma. Oncogene. 2011;30:4874–4886. doi: 10.1038/onc.2011.195. PubMed DOI PMC
Ohsawa M., Ikura Y., Fukushima H., Shirai N., Sugama Y., Suekane T., Hirayama M., Hino M., Ueda M. Immunohistochemical expression of multidrug resistance proteins as a predictor of poor response to chemotherapy and prognosis in patients with nodal diffuse large B-cell lymphoma. Oncology. 2005;68:422–431. doi: 10.1159/000086984. PubMed DOI
Greaves W., Xiao L., Sanchez-Espiridion B., Kunkalla K., Dave K.S., Liang C.S., Singh R.R., Younes A., Medeiros L.J., Vega F. Detection of ABCC1 expression in classical Hodgkin lymphoma is associated with increased risk of treatment failure using standard chemotherapy protocols. J. Hematol. Oncol. 2012;5:7. doi: 10.1186/1756-8722-5-47. PubMed DOI PMC
Wang J.-Q., Li J.Y., Teng Q.-X., Lei Z.-N., Ji N., Cui Q., Zeng L., Pan Y., Yang D.-H., Chen Z.-S. Venetoclax, a BCL-2 inhibitor, enhances the efficacy of chemotherapeutic agents in wild-type ABCG2-overexpression-mediated MDR cancer cells. Cancers. 2020;12:466. doi: 10.3390/cancers12020466. PubMed DOI PMC
Liu K., Song J., Yan Y., Zou K., Che Y., Wang B., Li Z., Yu W., Guo W., Zou L., et al. Melatonin increases the chemosensitivity of diffuse large B-cell lymphoma cells to epirubicin by inhibiting P-glycoprotein expression via the NF-κB pathway. Transl. Oncol. 2021;14:100876. doi: 10.1016/j.tranon.2020.100876. PubMed DOI PMC
Liu M., Gao H., He Y., Sun X., Zhang L. Upregulation of miR-101-3p Overcomes Ibrutinib Resistance by Targeting ABCC5 in Diffuse Large B-Cell Lymphoma (DLBCL) J. Hard. Tissue. Biol. 2023;32:11–20. doi: 10.2485/jhtb.32.11. DOI
Tsang T.J., Hsueh Y.C., Wei E.I., Lundy D.J., Cheng B., Chen Y.T., Wang S.S., Hsieh P.C.H. Subcellular localization of survivin determines its function in cardiomyocytes. Theranostics. 2017;7:4577–4590. doi: 10.7150/thno.20005. PubMed DOI PMC
Sah N.K., Seniya C. Survivin splice variants and their diagnostic significance. Tumor Biol. 2015;36:6623–6631. doi: 10.1007/s13277-015-3865-5. PubMed DOI
Bernardo P.S., Lemos L.G.T., de Moraes G.N., Maia R.C. Unraveling survivin expression in chronic myeloid leukemia: Molecular interactions and clinical implications. Blood Rev. 2020;43:100671. doi: 10.1016/j.blre.2020.100671. PubMed DOI
Zhang Y., Wang J., Sui X., Li Y., Lu K., Fang X., Jiang Y., Wang X. Prognostic and Clinicopathological Value of Survivin in Diffuse Large B-cell Lymphoma: A Meta-Analysis. Medicine. 2015;94:e1432. doi: 10.1097/MD.0000000000001432. PubMed DOI PMC
Mitrović Z., Ilić I., Aurer I., Kinda S.B., Radman I., Dotlić S., Ajdukovic R., Labar B. Prognostic Significance of Survivin and Caspase-3 Immunohistochemical Expression in Patients with Diffuse Large B-cell Lymphoma Treated with Rituximab and CHOP. Pathol. Oncol. Res. 2011;17:243–247. doi: 10.1007/s12253-010-9304-4. PubMed DOI
Liu Z., Xu-Monette Z.Y., Cao X., Manyam G.C., Wang X., Tzankov A., Xia Y., Li X., Visco C., Sun R., et al. Prognostic and biological significance of survivin expression in patients with diffuse large B-cell lymphoma treated with rituximab-CHOP therapy. Mod. Pathol. 2015;28:1297–1314. doi: 10.1038/modpathol.2015.94. PubMed DOI
Swerdlow S.H., Campo E., Pileri S.A., Harris N.L., Stein H., Siebert R., Advani R., Ghielmini M., Salles G.A., Zelenetz A.D., et al. The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood. 2016;127:2375–2390. doi: 10.1182/blood-2016-01-643569. PubMed DOI PMC
Lister T.A., Crowther D., Sutcliffe S.B., Glatstein E., Canellos G.P., Young R.C., Rosenberg S., Coltman C.A., Tubiana M. Report of a committee convened to discuss the evaluation and staging of patients with Hodgkin’s disease: Cotswolds meeting. J. Clin. Oncol. 1989;7:1630–1636. doi: 10.1200/JCO.1989.7.11.1630. PubMed DOI
Schwartz L.H., Litière S., de Vries E., Ford R., Gwyther S., Mandrekar S., Shankar L., Bogaerts J., Chen A., Dancey J., et al. RECIST 1.1-Update and clarification: From the RECIST committee. Eur. J. Cancer. 2016;62:132–137. doi: 10.1016/j.ejca.2016.03.081. PubMed DOI PMC
Cheson B.D., Horning S.J., Coiffier B., Shipp M.A., Fisher R.I., Connors J.M., Lister T.A., Vose J., Grillo-López A., Hagenbeek A., et al. Report of an international workshop to standardize response criteria for non-Hodgkin’s lymphomas. NCI Sponsored International Working Group. J. Clin. Oncol. 1999;17:1244. doi: 10.1200/JCO.1999.17.4.1244. PubMed DOI
Hans C.P., Weisenburger D.D., Greiner T.C., Gascoyne R.D., Delabie J., Ott G., Müller-Hermelink H., Campo E., Braziel R.M., Jaffe E.S., et al. Confirmation of the molecular classification of diffuse large B-cell lymphoma by immunohistochemistry using a tissue microarray. Blood. 2004;103:275–282. doi: 10.1182/blood-2003-05-1545. PubMed DOI
International Non-Hodgkin’s Lymphoma Prognostic Factors Project A predictive model for aggressive non-Hodgkin’s lymphoma. N. Engl. J. Med. 1993;329:987–994. doi: 10.1056/NEJM199309303291402. PubMed DOI
Nežić L., Škrbić R., Amidžić L., Gajanin R., Kuča K., Jaćević V. Simvastatin Protects Cardiomyocytes Against Endotoxin-induced Apoptosis and Up-regulates Survivin/NF-kB/p65 Expression. Sci. Rep. 2018;8:14652. doi: 10.1038/s41598-018-32376-4. PubMed DOI PMC
Nežić L., Amidžić L., Škrbić R., Gajanin R., Nepovimova E., Vališ M., Kuča K., Jaćević V. Simvastatin Inhibits Endotoxin-Induced Apoptosis in Liver and Spleen Through Up-Regulation of Survivin/NF-kB/p65 Expression. Front. Pharmacol. 2019;10:54. doi: 10.3389/fphar.2019.00054. PubMed DOI PMC
Szczuraszek K., Materna V., Halon A., Mazur G., Wróbel T., Kuliczkowski K., Maciejczyk A., Zabel M., Drag M., Dietel M., et al. Positive correlation between cyclooxygenase-2 and ABC-transporter expression in non-Hodgkin’s lymphomas. Oncol. Rep. 2009;22:1315–1323. doi: 10.3892/or_00000570. PubMed DOI
Tsuyama N., Sakata S., Baba S., Mishima Y., Nishimura N., Ueda K., Yokoyama M., Terui Y., Hatake K., Kitagawa M., et al. BCL2 expression in DLBCL: Reappraisal of immunohistochemistry with new criteria for therapeutic biomarker evaluation. Blood. 2017;130:489–500. doi: 10.1182/blood-2016-12-759621. PubMed DOI
Li L., Li Y., Que X., Gao X., Gao Q., Yu M., Ma K., Xi Y., Wang T. Prognostic significances of overexpression MYC and/or BCL2 in R-CHOP-treated diffuse large B-cell lymphoma: A Systematic review and meta-analysis. Sci. Rep. 2018;8:6267. doi: 10.1038/s41598-018-24631-5. PubMed DOI PMC
Krull J.E., Wenzl K., Hartert K.T., Manske M.K., Sarangi V., Maurer M.J., Larson M.C., Nowakowski G.S., Ansell S.M., McPhail E., et al. Somatic copy number gains in MYC, BCL2, and BCL6 identifies a subset of aggressive alternative-DH/TH DLBCL patients. Blood Cancer J. 2020;10:117. doi: 10.1038/s41408-020-00382-3. PubMed DOI PMC
Alaggio R., Amador C., Anagnostopoulos I., Attygalle A.D., Araujo I.B.O., Berti E., Bhagat G., Borges A.M., Boyer D., Calaminici M., et al. The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms. Leukemia. 2022;36:1720–1748. doi: 10.1038/s41375-022-01620-2. PubMed DOI PMC
Li L., Zhang X., Zhang T., Song Z., Hu G., Li W., Li L., Qiu L., Qian Z., Zhou S., et al. Prognostic Significance of BCL-2 and BCL-6 Expression in MYC-positive DLBCL. Clin. Lymphoma Myeloma Leuk. 2018;18:e381–e389. doi: 10.1016/j.clml.2018.06.010. PubMed DOI
Barraclough A., Alzahrani M., Ettrup M.S., Bishton M., van Vliet C., Farinha P., Gould C., Birch S., Sehn L.H., Sovani V., et al. COO and MYC/BCL2 status do not predict outcome among patients with stage I/II DLBCL: A retrospective multicenter study. Blood Adv. 2019;3:2013–2021. doi: 10.1182/bloodadvances.2019000251. PubMed DOI PMC
Camicia R., Winkler H.C., Hassa P.O. Novel drug targets for personalized precision medicine in relapsed/refractory diffuse large B-cell lymphoma: A comprehensive review. Mol. Cancer. 2015;14:207. doi: 10.1186/s12943-015-0474-2. PubMed DOI PMC
Andreadis C., Gimotty P.A., Wahl P., Hammond R., Houldsworth J., Schuster S.J., Rebbeck T.R. Members of the glutathione and ABC-transporter families are associated with clinical outcome in patients with diffuse large B-cell lymphoma. Blood. 2007;109:3409–3416. doi: 10.1182/blood-2006-09-047621. PubMed DOI PMC
Rujirojindakul P., Aiempanakit K., Kayasut K., Lekhakula A., Sriplung H. No Prognostic Impact of p53 and P-Glycoprotein Expression in Patients with Diffuse Large B-Cell Lymphoma. ISRN Oncol. 2011;2011:670358. doi: 10.5402/2011/670358. PubMed DOI PMC
Tabata M., Tsubaki M., Takeda T., Tateishi K., Tsurushima K., Imano M., Satou T., Ishizaka T., Nishida S. Dasatinib reverses drug resistance by downregulating MDR1 and Survivin in Burkitt lymphoma cells. BMC Complement. Med. Ther. 2020;20:84. doi: 10.1186/s12906-020-2879-8. PubMed DOI PMC
Steidl C., Telenius A., Shah S.P., Farinha P., Barclay L., Boyle M., Connors J.M., Horsman D.E., Gascoyne R.D. Genome-wide copy number analysis of Hodgkin Reed-Sternberg cells identifies recurrent imbalances with correlations to treatment outcome. Blood. 2010;116:418–427. doi: 10.1182/blood-2009-12-257345. PubMed DOI
Gündüz E., Dinçer M., Yıldız G., Bal C., Gülbaş Z. The frequency and clinical relevance of multidrug resistance protein expression in patients with lymphoma. Turk. J. Haematol. 2012;29:120–129. doi: 10.5505/tjh.2012.60362. PubMed DOI PMC
Markovic O., Marisavljevic D., Cemerikic-Martinovic V., Martinovic T., Filipovic B., Stanisavljevic D., Zivković R., Hajder J., Stanisavljevic N., Mihaljevic B. Survivin expression in patients with newly diagnosed nodal diffuse large B cell lymphoma (DLBCL) Med. Oncol. 2012;29:3515–3521. doi: 10.1007/s12032-012-0232-x. PubMed DOI PMC
Liu R., Chen Y., Liu G., Li C., Song Y., Cao Z., Li W., Hu J., Lu C., Liu Y. PI3K/AKT pathway as a key link modulates the multidrug resistance of cancers. Cell Death Dis. 2020;11:797. doi: 10.1038/s41419-020-02998-6. PubMed DOI PMC