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癌基因的生物学作用——来自血小板衍生生长因子的见解:罗兹纪念奖讲座

The biological role of oncogenes--insights from platelet-derived growth factor: Rhoads Memorial Award lecture.

作者信息

Stiles C D

出版信息

Cancer Res. 1985 Nov;45(11 Pt 1):5215-8.

PMID:2996757
Abstract

No one in tumor biology can now be unaware of the overlap between growth factors and oncogenes. Many if not all oncogenes are now perceived as functional components of a mitogenic cascade which is normally controlled by growth factors. Some oncogenes function at the onset of this cascade by directing the synthesis of an automitogenic growth factor. Others function in the interior of the cascade by directing synthesis of a growth factor receptor or a structurally altered receptor derivative. Still other oncogenes appear to be mutated or rearranged homologues of genes the expression of which is normally induced by growth factors. Those of us working with platelet-derived growth factor (PDGF) take particular satisfaction in this new conceptual framework. It is within the molecular biology of PDGF that the overlap between growth factors and oncogenes is illustrated to its fullest and most tangible extent. An oncogene termed c-sis directs synthesis of a functional PDGF subunit. The PDGF receptor protein is in all probability encoded by a member of the src family of oncogenes. Formation of the PDGF:receptor complex stimulates expression of the c-myc and c-fos protooncogenes. My associates and I have devoted the past 10 years to the molecular biology of PDGF. Our studies on the control of the 3T3 cell cycle by PDGF contributed a pair of new jargon terms to the oncology literature--"competence" and "progression." We also had some input into the bottom end of the "oncogene hierarchy" displayed in Chart 1. The effort that we invested paid a pleasant dividend for me when, in the spring of 1984, the American Association for Cancer Research honored me with the Rhoads Memorial Award. What follows is an overview of the PDGF literature which is more anecdotal than comprehensive. My object is to show how the PDGF field moved from the level of whole animal biology, through biochemistry, down to molecular genetics in just 10 years time.

摘要

肿瘤生物学领域的人现在都知道生长因子和癌基因之间存在重叠。现在,许多(即便不是全部)癌基因都被视为有丝分裂原级联反应的功能成分,而这一反应通常由生长因子控制。一些癌基因通过指导自分泌生长因子的合成在级联反应开始时发挥作用。另一些则通过指导生长因子受体或结构改变的受体衍生物的合成在级联反应内部发挥作用。还有一些癌基因似乎是基因的突变或重排同源物,这些基因的表达通常由生长因子诱导。我们这些从事血小板衍生生长因子(PDGF)研究的人对这个新的概念框架特别满意。正是在PDGF的分子生物学中,生长因子和癌基因之间的重叠得到了最充分、最切实的体现。一个名为c-sis的癌基因指导功能性PDGF亚基的合成。PDGF受体蛋白很可能由src癌基因家族的一个成员编码。PDGF:受体复合物的形成刺激c-myc和c-fos原癌基因的表达。我和我的同事们在过去10年里致力于PDGF的分子生物学研究。我们关于PDGF对3T3细胞周期控制的研究为肿瘤学文献贡献了一对新的术语——“感受态”和“进展”。我们还对图1所示的“癌基因层级”的底层有一些贡献。1984年春天,美国癌症研究协会授予我罗兹纪念奖,我们付出的努力给我带来了一份惊喜。接下来是对PDGF文献的概述,与其说是全面的,不如说是轶事性的。我的目的是展示PDGF领域是如何在短短10年时间里从全动物生物学层面,经过生物化学,发展到分子遗传学层面的。

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