Mcl-1 is a potential therapeutic target in multiple types of cancer

被引:302
作者
Akgul, C. [1 ]
机构
[1] Canakkale Onsekiz Mart Univ, Fac Arts & Sci, Dept Chem, Biochem Res Grp, TR-17100 Canakkale, Turkey
关键词
Apoptosis; cancer; Bcl-2; family; Mcl-1; therapeutic; BCL-2; FAMILY-MEMBERS; MYELOID CELL LEUKEMIA-1; HISTONE DEACETYLASE INHIBITOR; RECEPTOR-MEDIATED APOPTOSIS; SMALL-MOLECULE INHIBITORS; HUMAN-MELANOMA CELLS; DOWN-REGULATION; ANTISENSE OLIGONUCLEOTIDES; PROTEIN FAMILY; BREAST-CANCER;
D O I
10.1007/s00018-008-8637-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Resistance to apoptosis is a common challenge in human malignancies contributing to both progress of cancer and resistance to conventional therapeutics. Abnormalities in a variety of cell intrinsic and extrinsic molecular mechanisms cooperatively promote tumor formation. Therapeutic approaches that specifically target components of these molecular mechanisms are getting widespread attention. Mcl-1 is a highly expressed pro-survival protein in human malignancies and its cellular expression is tightly regulated via multiple mechanisms. Mcl-1 differs from other members of the Bcl-2 family in having a very short half-life. So inhibition of its expression and/or neutralization of its anti-apoptotic function will rapidly make Mcl-1-dependent cells more susceptible to apoptosis and provide an opportunity to combat several types of cancers. This review summarizes the current knowledge on the regulation of Mcl-1 expression and discusses the alternative approaches targeting Mcl-1 in human cancer cells whose survivals mainly depend on Mcl-1.
引用
收藏
页码:1326 / 1336
页数:11
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