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Multiple Myeloma, Gammopathies

Dexamethasone treatment promotes Bcl-2 dependence in multiple myeloma resulting in sensitivity to venetoclax

Abstract

Venetoclax (ABT-199), a specific inhibitor of the anti-apoptotic protein Bcl-2, is currently in phase I clinical trials for multiple myeloma. The results suggest that venetoclax is only active in a small cohort of patients therefore we wanted to determine its efficacy when used in combination. Combining venetoclax with melphalan or carfilzomib produced additive or better cell death in four of the five cell lines tested. The most striking results were seen with dexamethasone (Dex). Co-treatment of human myeloma cell lines and primary patient samples, with Dex and venetoclax, significantly increased cell death over venetoclax alone in four of the five cell lines, and in all patient samples tested. The mechanism by which this occurs is an increase in the expression of both Bcl-2 and Bim upon addition of Dex. This results in alterations in Bim binding to anti-apoptotic proteins. Dex shifts Bim binding towards Bcl-2 resulting in increased sensitivity to venetoclax. These data suggest that knowledge of drug-induced alterations of Bim-binding patterns may help inform better combination drug regimens. Furthermore, the data indicate combining this novel therapeutic with Dex could be an effective therapy for a broader range of patients than would be predicted by single-agent activity.

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References

  1. Cancer Facts & Figures. American Cancer Society; 2015.

  2. Certo M, Del Gaizo Moore V, Nishino M, Wei G, Korsmeyer S, Armstrong SA et al. Mitochondria primed by death signals determine cellular addiction to antiapoptotic BCL-2 family members. Cancer Cell 2006; 9: 351–365.

    Article  CAS  PubMed  Google Scholar 

  3. Chipuk JE, Moldoveanu T, Llambi F, Parsons MJ, Green DR . The BCL-2 family reunion. Mol Cell 2010; 37: 299–310.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Davids MS, Letai A . Targeting the B-cell lymphoma/leukemia 2 family in cancer. J Clin Oncol 2012; 30: 3127–3135.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Kuroda J, Taniwaki M . Involvement of BH3-only proteins in hematologic malignancies. Crit Rev Oncol Hematol 2009; 71: 89–101.

    Article  PubMed  Google Scholar 

  6. Tait SW, Green DR . Mitochondria and cell death: outer membrane permeabilization and beyond. Nat Rev Mol Cell Biol 2010; 11: 621–632.

    Article  CAS  PubMed  Google Scholar 

  7. Oltersdorf T, Elmore SW, Shoemaker AR, Armstrong RC, Augeri DJ, Belli BA et al. An inhibitor of Bcl-2 family proteins induces regression of solid tumours. Nature 2005; 435: 677–681.

    Article  CAS  PubMed  Google Scholar 

  8. Tse C, Shoemaker AR, Adickes J, Anderson MG, Chen J, Jin S et al. ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor. Cancer Res 2008; 68: 3421–3428.

    Article  CAS  PubMed  Google Scholar 

  9. Del Gaizo Moore V, Brown JR, Certo M, Love TM, Novina CD, Letai A . Chronic lymphocytic leukemia requires BCL2 to sequester prodeath BIM, explaining sensitivity to BCL2 antagonist ABT-737. J Clin Invest 2007; 117: 112–121.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Del Gaizo Moore V, Schlis KD, Sallan SE, Armstrong SA, Letai A . BCL-2 dependence and ABT-737 sensitivity in acute lymphoblastic leukemia. Blood 2008; 111: 2300–2309.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Hann CL, Daniel VC, Sugar EA, Dobromilskaya I, Murphy SC, Cope L et al. Therapeutic efficacy of ABT-737, a selective inhibitor of BCL-2, in small cell lung cancer. Cancer Res 2008; 68: 2321–2328.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Schoenwaelder SM, Jarman KE, Gardiner EE, Hua M, Qiao J, White MJ et al. Bcl-xL-inhibitory BH3 mimetics can induce a transient thrombocytopathy that undermines the hemostatic function of platelets. Blood 2011; 118: 1663–1674.

    Article  CAS  PubMed  Google Scholar 

  13. Souers AJ, Leverson JD, Boghaert ER, Ackler SL, Catron ND, Chen J et al. ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets. Nat Med 2013; 19: 202–208.

    Article  CAS  PubMed  Google Scholar 

  14. Pan R, Hogdal LJ, Benito JM, Bucci D, Han L, Borthakur G et al. Selective BCL-2 inhibition by ABT-199 causes on-target cell death in acute myeloid leukemia. Cancer Discov 2014; 4: 362–375.

    Article  CAS  PubMed  Google Scholar 

  15. Touzeau C, Dousset C, Le Gouill S, Sampath D, Leverson JD, Souers AJ et al. The Bcl-2 specific BH3 mimetic ABT-199: a promising targeted therapy for t(11;14) multiple myeloma. Leukemia 2014; 28: 210–212.

    Article  CAS  PubMed  Google Scholar 

  16. Morales AA, Kurtoglu M, Matulis SM, Liu J, Siefker D, Gutman DM et al. Distribution of Bim determines Mcl-1 dependence or codependence with Bcl-xL/Bcl-2 in Mcl-1-expressing myeloma cells. Blood 2011; 118: 1329–1339.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Morales AA, Gutman D, Lee KP, Boise LH . BH3-only proteins Noxa, Bmf, and Bim are necessary for arsenic trioxide-induced cell death in myeloma. Blood 2008; 111: 5152–5162.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Grad JM, Bahlis NJ, Reis I, Oshiro MM, Dalton WS, Boise LH . Ascorbic acid enhances arsenic trioxide-induced cytotoxicity in multiple myeloma cells. Blood 2001; 98: 805–813.

    Article  CAS  PubMed  Google Scholar 

  19. Boise LH, Minn AJ, Noel PJ, June CH, Accavitti MA, Lindsten T et al. CD28 costimulation can promote T cell survival by enhancing the expression of Bcl-XL. Immunity 1995; 3: 87–98.

    Article  CAS  PubMed  Google Scholar 

  20. Attal M, Harousseau JL, Stoppa AM, Sotto JJ, Fuzibet JG, Rossi JF et al. A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma. Intergroupe Francais du Myelome. N Engl J Med 1996; 335: 91–97.

    Article  CAS  PubMed  Google Scholar 

  21. Gupta VA, Nooka AK, Lonial S, Boise LH . Clinical potential of carfilzomib in the treatment of relapsed and refractory multiple myeloma. Blood Lymphat Cancer 2013; 3: 41.

    CAS  Google Scholar 

  22. Fennell DA, Chacko A, Mutti L . BCL-2 family regulation by the 20 S proteasome inhibitor bortezomib. Oncogene 2008; 27: 1189–1197.

    Article  CAS  PubMed  Google Scholar 

  23. Jing D, Bhadri VA, Beck D, Thoms JA, Yakob NA, Wong JW et al. Opposing regulation of BIM and BCL2 controls glucocorticoid-induced apoptosis of pediatric acute lymphoblastic leukemia cells. Blood 2015; 125: 273–283.

    Article  CAS  PubMed  Google Scholar 

  24. Touzeau C, Ryan J, Guerriero JL, Moreau P, Chonghaile TN, Le Gouill S et al. BH3-profiling identifies heterogeneous dependency on Bcl-2 family members in multiple myeloma and predicts sensitivity to BH3 mimetics. Leukemia 2015; 29: 1–4.

    Article  Google Scholar 

  25. Montero J, Sarosiek KA, DeAngelo JD, Maertens O, Ryan J, Ercan D et al. Drug-induced death signaling strategy rapidly predicts cancer response to chemotherapy. Cell 2015; 160: 977–989.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Kumar S, Vij R, Kaufman JL, Mikhael J, Facon T, Moreau P et al. Phase I interim safety and efficacy of venetoclax (ABT-199/GDC-0199) monotherapy for relapsed/refractory (R/R) multiple myeloma (MM). J Clin Oncol 2015; 33: 8576.

    Google Scholar 

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Correspondence to L H Boise.

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Competing interests

LHB, SL and JLK have all served as consultants to Onyx Pharmaceuticals, the makers of carfilzomib. The remaining authors declare no conflict of interest.

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Supplementary Information accompanies this paper on the Leukemia website

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Matulis, S., Gupta, V., Nooka, A. et al. Dexamethasone treatment promotes Bcl-2 dependence in multiple myeloma resulting in sensitivity to venetoclax. Leukemia 30, 1086–1093 (2016). https://doi.org/10.1038/leu.2015.350

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