MiRNA-16-1 Suppresses Mcl-1 and Bcl-2 and Sensitizes Chronic Lymphocytic Leukemia Cells to BH3 Mimetic ABT-199

被引:3
|
作者
Ashofteh, Nooshin [1 ]
Mehbod, Amir Sayed Ali [2 ]
Bayat, Mohammad [3 ]
Karami, Hadi [1 ,4 ]
机构
[1] Arak Univ Med Sci, Fac Med, Dept Mol Med & Biotechnol, Arak, Iran
[2] AJA Univ Med Sci, Sch Med, Dept Parasitol & Mycol, Tehran, Iran
[3] Arak Univ Med Sci, Fac Med, Dept Anat, Arak, Iran
[4] Arak Univ Med Sci, Fac Med, Dept Mol Med andBiotechnol, POB 3848176941, Arak, Iran
关键词
ABT-199; Bcl-2; Chronic Lymphocytic Leukemia; Mcl-1; TARGETED THERAPY; APOPTOSIS; RESISTANCE; MICRORNA; INCREASES;
D O I
10.22074/cellj.2022.8101
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: Chronic lymphoid leukemia (CLL) is the most common type of leukemia among adults. Increased levels of Mcl-1 and Bcl-xL is linked to resistance to Bcl-2 inhibitors including ABT-199. In this study, we investigated the effect of miRNA-16-1 on apoptosis and sensitivity of the CLL cells to ABT-199. Materials and Methods: In this experimental study, the Mcl-1 and Bcl-2 expression were measured using qualitative reverse transcription-polymerase chain reaction (qRT-PCR) and western blotting. The effect of treatments on cell survival and growth were explored with MTT assay and Trypan blue assay, respectively. The drug interaction was evaluated using combination index analysis. Apoptosis was assessed by ELISA cell death and caspase-3 activity assays. Results: MiRNA-16-1 markedly inhibited the expression of Mcl-1 and Bcl-2 in a time dependent manner (P < 0.05, relative to blank control). Pretreatment with miRNA-16-1 synergistically suppressed the cell growth and survival and reduced the half -maximal inhibitory concentration (IC50) value of ABT-199. Moreover, miRNA-16-1 markedly augmented the apoptotic effect of ABT-199 in CLL cells (P < 0.05). Conclusion: Our findings propose that miRNA-16-1 act in concert with ABT-199 to exert synergistic anticancer efficacy against CLL, which is attributed to the inhibition of Bcl-2 and Mcl-1. This may propose a promising strategy for CLL resistant patients.
引用
收藏
页码:473 / 480
页数:8
相关论文
共 50 条
  • [1] Targeting BCL-2 with the BH3 mimetic ABT-199 in ER-positive breast cancer
    Lindeman, G. J.
    Vaillant, F.
    Merino, D.
    Lee, L.
    Breslin, K.
    Pal, B.
    Ritchie, M. E.
    Smyth, G. K.
    Christie, M.
    Phillipson, L. J.
    Burns, C. J.
    Mann, G. B.
    Visvader, J. E.
    CANCER RESEARCH, 2013, 73
  • [2] BCL-2-Selective BH3 Mimetic ABT-199 Is a Potent Agent For Acute Myeloid Leukemia
    Pan, Rongqing
    Debose, LaKeisha
    Benito, Juliana M.
    Golfman, Leonard S.
    Zweidler-McKay, Patrick A.
    Han, Lina
    Harutyunyan, Karine G.
    Mu, Hong
    Ruvolo, Vivian R.
    Park, Eugene
    Muschen, Markus
    Leverson, Joel
    Borthakur, Gautam
    Kantarjian, Hagop M.
    Ruvolo, Peter P.
    Andreeff, Michael
    Konopleva, Marina
    BLOOD, 2013, 122 (21)
  • [3] Targeting BCL-2 with the BH3 Mimetic ABT-199 in Estrogen Receptor-Positive Breast Cancer
    Vaillant, Francois
    Merino, Delphine
    Lee, Lily
    Breslin, Kelsey
    Pal, Bhupinder
    Ritchie, Matthew E.
    Smyth, Gordon K.
    Christie, Michael
    Phillipson, Louisa J.
    Burns, Christopher J.
    Mann, G. Bruce
    Visvader, Jane E.
    Lindeman, Geoffrey J.
    CANCER CELL, 2013, 24 (01) : 120 - 129
  • [4] An immunoassay detecting Bcl-2: Bim and Mcl-1: Bim complexes in the phase 1 monotherapy study of the Bcl-2 inhibitor, ABT-199/GDC-0199, in chronic lymphocytic leukemia patients
    Li, Jessica
    Chen, Jun
    Kadel, Ward
    Chyla, Brenda
    McKeegan, Evelyn
    Punnoose, Elizabeth
    Darbonne, Walter
    CANCER RESEARCH, 2014, 74 (19)
  • [5] SELECTIVE INHIBITION OF BCL-2 IS ACTIVE AGAINST CHRONIC LYMPHOCYTIC LEUKEMIA (CLL): FIRST CLINICAL EXPERIENCE WITH THE BH3-MIMETIC ABT-199
    Roberts, A.
    Davids, M.
    Mahadevan, D.
    Anderson, M.
    Kipps, T.
    Pagel, J.
    Kahl, B.
    Wierda, W.
    Darden, D.
    Nolan, C.
    Xiong, H.
    Huang, D.
    Chyla, B.
    Busman, T.
    Cerri, E.
    Enschede, S.
    Humerickhouse, R.
    Seymour, J.
    HAEMATOLOGICA, 2012, 97 : 219 - 220
  • [6] MCL-1 or BCL-xL-dependent resistance to the BCL-2 antagonist (ABT-199) can be overcome by specific inhibitor as single agents and in combination with ABT-199 in acute myeloid leukemia cells
    Wang, Qing
    Wan, Jiangbo
    Zhang, Wenhao
    Hao, Siguo
    LEUKEMIA & LYMPHOMA, 2019, 60 (09) : 2170 - 2180
  • [7] A potent and selective small molecule inhibitor of MCL-1 sensitizes DLBCL cell lines to the BCL-2 selective inhibitor ABT-199
    Phillips, D. C.
    Xiao, Y.
    Lam, L.
    Litinovic, E.
    Roberts-Rapp, L.
    Souers, A. J.
    Leverson, J. D.
    EUROPEAN JOURNAL OF CANCER, 2014, 50 : 130 - 130
  • [8] Bcl-2 phosphorylation confers resistance on chronic lymphocytic leukaemia cells to the BH3 mimetics ABT-737, ABT-263 and ABT-199 by impeding direct binding
    Song, Ting
    Chai, Gaobo
    Liu, Yubo
    Yu, Xiaoyan
    Wang, Ziqian
    Zhang, Zhichao
    BRITISH JOURNAL OF PHARMACOLOGY, 2016, 173 (03) : 471 - 483
  • [9] MNDA controls the expression of MCL-1 and BCL-2 in chronic lymphocytic leukemia cells
    Bottardi, Stefania
    Guieze, Romain
    Bourgoin, Vincent
    Fotouhi-Ardakani, Nasser
    Douge, Aurore
    Darracq, Anais
    Lakehal, Yahia A.
    Berger, Marc G.
    Mollica, Luigina
    Bay, Jacques-Olivier
    Omichinski, James G.
    Milot, Eric
    EXPERIMENTAL HEMATOLOGY, 2020, 88 : 68 - +
  • [10] The Bcl-2 specific BH3 mimetic ABT-199: a promising targeted therapy for t(11;14) multiple myeloma
    C Touzeau
    C Dousset
    S Le Gouill
    D Sampath
    J D Leverson
    A J Souers
    S Maïga
    M C Béné
    P Moreau
    C Pellat-Deceunynck
    M Amiot
    Leukemia, 2014, 28 : 210 - 212