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本文引用的文献

1
Deciphering the rules of programmed cell death to improve therapy of cancer and other diseases.解析细胞程序性死亡的规律以提高癌症和其他疾病的治疗效果。
EMBO J. 2011 Aug 23;30(18):3667-83. doi: 10.1038/emboj.2011.307.
2
Transient binding of an activator BH3 domain to the Bak BH3-binding groove initiates Bak oligomerization.瞬时结合激活剂 BH3 结构域到 Bak BH3 结合沟启动 Bak 寡聚化。
J Cell Biol. 2011 Jul 11;194(1):39-48. doi: 10.1083/jcb.201102027. Epub 2011 Jul 4.
3
Non-apoptotic role of BID in inflammation and innate immunity.BID 在炎症和天然免疫中的非凋亡作用。
Nature. 2011 Jun 2;474(7349):96-9. doi: 10.1038/nature09982. Epub 2011 May 8.
4
Deciphering the molecular events necessary for synergistic tumor cell apoptosis mediated by the histone deacetylase inhibitor vorinostat and the BH3 mimetic ABT-737.解析组蛋白去乙酰化酶抑制剂伏立诺他和 BH3 模拟物 ABT-737 协同诱导肿瘤细胞凋亡所必需的分子事件。
Cancer Res. 2011 May 15;71(10):3603-15. doi: 10.1158/0008-5472.CAN-10-3289. Epub 2011 Mar 11.
5
Oncogenic Ras-induced expression of Noxa and Beclin-1 promotes autophagic cell death and limits clonogenic survival.致癌性 Ras 诱导 Noxa 和 Beclin-1 的表达促进自噬性细胞死亡并限制集落形成能力的存活。
Mol Cell. 2011 Apr 8;42(1):23-35. doi: 10.1016/j.molcel.2011.02.009. Epub 2011 Feb 25.
6
Phase I study of Navitoclax (ABT-263), a novel Bcl-2 family inhibitor, in patients with small-cell lung cancer and other solid tumors.Navitoclax(ABT-263)治疗小细胞肺癌和其他实体瘤患者的 I 期临床研究。Navitoclax 是一种新型 Bcl-2 家族抑制剂。
J Clin Oncol. 2011 Mar 1;29(7):909-16. doi: 10.1200/JCO.2010.31.6208. Epub 2011 Jan 31.
7
Glucocorticoid-mediated repression of the oncogenic microRNA cluster miR-17~92 contributes to the induction of Bim and initiation of apoptosis.糖皮质激素介导的致癌性微小RNA簇miR-17~92的抑制作用有助于Bim的诱导和细胞凋亡的启动。
Mol Endocrinol. 2011 Mar;25(3):409-20. doi: 10.1210/me.2010-0402. Epub 2011 Jan 14.
8
The proapoptotic function of Noxa in human leukemia cells is regulated by the kinase Cdk5 and by glucose.Noxa 在人白血病细胞中的促凋亡功能受激酶 Cdk5 和葡萄糖调节。
Mol Cell. 2010 Dec 10;40(5):823-33. doi: 10.1016/j.molcel.2010.11.035.
9
Navitoclax, a targeted high-affinity inhibitor of BCL-2, in lymphoid malignancies: a phase 1 dose-escalation study of safety, pharmacokinetics, pharmacodynamics, and antitumour activity.纳维托昔单抗,一种靶向高亲和力的 BCL-2 抑制剂,用于淋巴恶性肿瘤:安全性、药代动力学、药效学和抗肿瘤活性的 1 期剂量递增研究。
Lancet Oncol. 2010 Dec;11(12):1149-59. doi: 10.1016/S1470-2045(10)70261-8. Epub 2010 Nov 18.
10
Evidence that inhibition of BAX activation by BCL-2 involves its tight and preferential interaction with the BH3 domain of BAX.证据表明,BCL-2 通过抑制 BAX 的激活涉及 BAX 的 BH3 结构域的紧密和优先相互作用。
Cell Res. 2011 Apr;21(4):627-41. doi: 10.1038/cr.2010.149. Epub 2010 Nov 9.

BH3-only proteins in apoptosis at a glance.

作者信息

Happo Lina, Strasser Andreas, Cory Suzanne

机构信息

The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, Melbourne, VIC 3052, Australia.

出版信息

J Cell Sci. 2012 Mar 1;125(Pt 5):1081-7. doi: 10.1242/jcs.090514.

DOI:10.1242/jcs.090514
PMID:22492984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3324577/
Abstract
摘要