Mcl-1: A gateway to TRAIL sensitization

被引:97
|
作者
Kim, Seok-Hyun
Ricci, M. Stacey
Ei-Deiry, Wafik S.
机构
[1] Univ Penn, Sch Med, Lab Mol Oncol & Cell Cycle Regulat, Inst Translat Med & Therapeut,Dept Med Hematol On, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Lab Mol Oncol & Cell Cycle Regulat, Inst Translat Med & Therapeut,Dept Genet, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Lab Mol Oncol & Cell Cycle Regulat, Inst Translat Med & Therapeut,Dept Pharmacol, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Abramson Comprehens Canc Ctr, Philadelphia, PA 19104 USA
关键词
D O I
10.1158/0008-5472.CAN-07-6278
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The proapoptotic cytokine tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is being evaluated presently as a selective anticancer agent, but its limited effects against cancer cell lines has raised some concerns about its ultimate clinical utility. Here, we review recent findings that cancer cell sensitivity to TRAIL is greatly increased when the Bcl-2 family protein Mcl-1 is down-regulated by the Raf/vascular endothelial growth factor kinase inhibitor sorafenib, a Food and Drug Administration-approved cancer drug. Using the TRAIL-sorafenib combination as a tactic to more effectively kill cancer cells may provide an effective tool to attack a variety of human cancers that are largely presently untreatable.
引用
收藏
页码:2062 / 2064
页数:3
相关论文
共 50 条
  • [1] Countering TRAIL resistance in melanoma cells by Mcl-1 silencing
    Sarif, Z.
    Tolksdorf, B.
    Fechner, H.
    Eberle, J.
    EXPERIMENTAL DERMATOLOGY, 2023, 32 (04) : E106 - E106
  • [2] Overcoming TRAIL Resistance in Melanoma Cells by Mcl-1 Silencing
    Sarif, Z.
    Tolksdorf, B.
    Fechner, H.
    Eberle, J.
    JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT, 2019, 17 : 30 - 30
  • [3] Mcl-1
    Michels, J
    Johnson, PWM
    Packham, G
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2005, 37 (02): : 267 - 271
  • [4] Modulation of Mcl-1 sensitizes glioblastoma to TRAIL-induced apoptosis
    Á. C. Murphy
    B. Weyhenmeyer
    J. Noonan
    S. M. Kilbride
    S. Schimansky
    K. P. Loh
    D. Kögel
    A. G. Letai
    J. H. M. Prehn
    B. M. Murphy
    Apoptosis, 2014, 19 : 629 - 642
  • [5] Modulation of Mcl-1 sensitizes glioblastoma to TRAIL-induced apoptosis
    Murphy, A. C.
    Weyhenmeyer, B.
    Noonan, J.
    Kilbride, S. M.
    Schimansky, S.
    Loh, K. P.
    Koegel, D.
    Letai, A. G.
    Prehn, J. H. M.
    Murphy, B. M.
    APOPTOSIS, 2014, 19 (04) : 629 - 642
  • [6] MCL-1 inhibits BAX in the absence of MCL-1/BAX interaction
    Germain, Marc
    Milburn, Jocelyn
    Duronio, Vincent
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (10) : 6384 - 6392
  • [7] Mcl-1 targeting strategies unlock the proapoptotic potential of TRAIL in melanoma cells
    Sarif, Zina
    Tolksdorf, Beatrice
    Fechner, Henry
    Eberle, Juergen
    MOLECULAR CARCINOGENESIS, 2020, 59 (11) : 1256 - 1268
  • [8] Puma*Mcl-1 interaction is not sufficient to prevent rapid degradation of Mcl-1
    Yide Mei
    Wenjing Du
    Yonghui Yang
    Mian Wu
    Oncogene, 2005, 24 : 7224 - 7237
  • [9] Mcl-1: the 1 in CLL
    Gandhi, Varsha
    Balakrishnan, Kumudha
    Chen, Lisa S.
    BLOOD, 2008, 112 (09) : 3538 - 3540
  • [10] Puma* Mcl-1 interaction is not sufficient to prevent rapid degradation of Mcl-1
    Mei, YD
    Du, WJ
    Yang, YH
    Wu, MA
    ONCOGENE, 2005, 24 (48) : 7224 - 7237