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诱导分化、细胞周期与癌症治疗

Induced differentiation, the cell cycle, and the treatment of cancer.

作者信息

Rifkind R A, Richon V M, Marks P A

机构信息

Dewitt Wallace Research Laboratory, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

Pharmacol Ther. 1996;69(2):97-102. doi: 10.1016/0163-7258(95)02044-6.

Abstract

Hybrid polar compounds, of which hexamethylene bisacetamide (HMBA) is the prototype, have been shown to be potent inducers of differentiation of many types of transformed cells. With virus-transformed murine erythroleukemia cells as a model, HMBA was shown to cause these cells to arrest in G1 phase and express globin genes. HMBA action involves modulation of factors regulating G1 to S phase progression, including a decrease in the G1 cyclin-dependent kinase 4 accumulation of underphosphorylated retinoblastoma protein, and an increase in the level of both retinoblastoma protein and the related protein, p107. In turn, p107 complexes with transcription factors such as E2F and, presumably, inhibits transcriptional activity of these factors for genes whose products are required for DNA synthesis. This provides a possible mechanism for HMBA-induced terminal cell division of transformed cells. Evidence that hybrid polar compounds have therapeutic potential for cancer treatment is also reviewed.

摘要

以六亚甲基双乙酰胺(HMBA)为原型的杂化极性化合物已被证明是多种类型转化细胞分化的有效诱导剂。以病毒转化的小鼠红白血病细胞为模型,HMBA被证明可使这些细胞停滞在G1期并表达珠蛋白基因。HMBA的作用涉及调节G1期到S期进程的因子,包括G1期细胞周期蛋白依赖性激酶4的减少、低磷酸化视网膜母细胞瘤蛋白的积累,以及视网膜母细胞瘤蛋白和相关蛋白p107水平的增加。反过来,p107与诸如E2F等转录因子结合,并且推测会抑制这些因子对DNA合成所需产物基因的转录活性。这为HMBA诱导转化细胞的终末细胞分裂提供了一种可能的机制。本文还综述了杂化极性化合物具有癌症治疗潜力的证据。

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