Apoptosis and cancer mechanisms.

Cancer surveys Pub Date : 1997-01-01
H Pan, C Yin, T Van Dyke
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Abstract

For nearly two decades, studies in the cancer research field focussed on identifying genes that act as positive and negative regulators of cell growth. Only relatively recently was it recognized that the regulation of cell death (apoptosis) is also an important modulator of tumorigenesis. At least two genes linked to human cancers, BCL2 and TP53, have been shown to regulate apoptosis. The correlation between apoptosis modulating genes and human tumours raises an important question as to how dysregulation of apoptosis contributes to neoplastic transformation and malignant cell growth. Cell culture studies have clearly demonstrated that TP53 can induce and BCL2 can suppress apoptosis in response to various stimuli. Studies of mammalian viruses, which possess mechanisms for both inducing and evading apoptosis, have also extended our understanding of this process. On the basis of such findings, several animal models have been developed which begin to address the role of apoptosis regulation in tumorigenesis. This chapter discusses those animal models, focussing on bcl-2 (and its relatives) and p53.

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细胞凋亡和癌症机制。
近二十年来,癌症研究领域的研究集中在识别细胞生长的积极和消极调节基因上。直到最近,人们才认识到细胞死亡(凋亡)的调节也是肿瘤发生的重要调节剂。至少有两个与人类癌症相关的基因,BCL2和TP53,已经被证明可以调节细胞凋亡。细胞凋亡调节基因与人类肿瘤之间的相关性提出了一个重要的问题,即细胞凋亡失调如何促进肿瘤转化和恶性细胞生长。细胞培养研究清楚地表明,在各种刺激下,TP53可以诱导细胞凋亡,BCL2可以抑制细胞凋亡。对哺乳动物病毒的研究也扩展了我们对这一过程的理解,这些病毒具有诱导和逃避细胞凋亡的机制。在这些发现的基础上,已经建立了一些动物模型,开始解决细胞凋亡调节在肿瘤发生中的作用。本章讨论这些动物模型,重点是bcl-2(及其近亲)和p53。
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