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PUMA可诱导结肠癌细胞迅速凋亡。

PUMA induces the rapid apoptosis of colorectal cancer cells.

作者信息

Yu J, Zhang L, Hwang P M, Kinzler K W, Vogelstein B

机构信息

The Johns Hopkins Oncology Center, The Johns Hopkins Medical Institutions, Baltimore, Maryland 21231, USA.

出版信息

Mol Cell. 2001 Mar;7(3):673-82. doi: 10.1016/s1097-2765(01)00213-1.

DOI:10.1016/s1097-2765(01)00213-1
PMID:11463391
Abstract

Through global profiling of genes that were expressed soon after p53 expression, we identified a novel gene termed PUMA (p53 upregulated modulator of apoptosis). The protein encoded by PUMA was found to be exclusively mitochondrial and to bind to Bcl-2 and Bcl-X(L) through a BH3 domain. Exogenous expression of PUMA resulted in an extremely rapid and profound apoptosis that occurred much earlier than that resulting from exogenous expression of p53. Based on its unique expression patterns, p53 dependence, and biochemical properties, PUMA may be a direct mediator of p53-associated apoptosis.

摘要

通过对p53表达后不久即表达的基因进行全基因组分析,我们鉴定出一个名为PUMA(p53上调的凋亡调节因子)的新基因。发现由PUMA编码的蛋白质仅存在于线粒体中,并通过一个BH3结构域与Bcl-2和Bcl-X(L)结合。PUMA的外源性表达导致极其快速且深刻的凋亡,其发生时间比p53外源性表达所导致的凋亡要早得多。基于其独特的表达模式、对p53的依赖性及生化特性,PUMA可能是p53相关凋亡的直接介导因子。

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PUMA induces the rapid apoptosis of colorectal cancer cells.PUMA可诱导结肠癌细胞迅速凋亡。
Mol Cell. 2001 Mar;7(3):673-82. doi: 10.1016/s1097-2765(01)00213-1.
2
PUMA, a novel proapoptotic gene, is induced by p53.PUMA是一种新型促凋亡基因,由p53诱导产生。
Mol Cell. 2001 Mar;7(3):683-94. doi: 10.1016/s1097-2765(01)00214-3.
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PUMA couples the nuclear and cytoplasmic proapoptotic function of p53.PUMA将p53的核内和胞质促凋亡功能联系起来。
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Noxa induces apoptosis in oncogene-expressing cells through catch-and-release mechanism operating between Puma and Mcl-1.NOXA 通过 Puma 和 Mcl-1 之间的“捕获-释放”机制诱导癌基因表达细胞发生凋亡。
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Noxa, a BH3-only member of the Bcl-2 family and candidate mediator of p53-induced apoptosis.Noxa,一种仅含BH3结构域的Bcl-2家族成员,是p53诱导凋亡的潜在介导因子。
Science. 2000 May 12;288(5468):1053-8. doi: 10.1126/science.288.5468.1053.
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Puma(*)Mcl-1 interaction is not sufficient to prevent rapid degradation of Mcl-1.彪马(*)与髓细胞白血病-1(Mcl-1)的相互作用不足以阻止Mcl-1的快速降解。
Oncogene. 2005 Nov 3;24(48):7224-37. doi: 10.1038/sj.onc.1208873.
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PUMA overexpression induces reactive oxygen species generation and proteasome-mediated stathmin degradation in colorectal cancer cells.PUMA过表达诱导大肠癌细胞中活性氧的产生及蛋白酶体介导的Stathmin降解。
Cancer Res. 2005 Mar 1;65(5):1647-54. doi: 10.1158/0008-5472.CAN-04-1754.
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Transcriptional upregulation of PUMA modulates endoplasmic reticulum calcium pool depletion-induced apoptosis via Bax activation.PUMA 的转录上调通过 Bax 激活调节内质网钙库耗竭诱导的细胞凋亡。
Cell Death Differ. 2005 Oct;12(10):1310-8. doi: 10.1038/sj.cdd.4401659.
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Regulation of PUMA-alpha by p53 in cisplatin-induced renal cell apoptosis.p53对顺铂诱导的肾细胞凋亡中PUMA-α的调控
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The nuclear function of p53 is required for PUMA-mediated apoptosis induced by DNA damage.p53的核功能是DNA损伤诱导的PUMA介导的细胞凋亡所必需的。
Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):4054-9. doi: 10.1073/pnas.0700020104. Epub 2007 Feb 28.

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