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本文引用的文献

1
Transcription factor Stat5 knockdown enhances androgen receptor degradation and delays castration-resistant prostate cancer progression in vivo.转录因子 Stat5 敲低增强雄激素受体降解并延缓体内去势抵抗性前列腺癌的进展。
Mol Cancer Ther. 2011 Feb;10(2):347-59. doi: 10.1158/1535-7163.MCT-10-0850. Epub 2011 Jan 7.
2
Stat5 promotes survival of mammary epithelial cells through transcriptional activation of a distinct promoter in Akt1.Stat5 通过 Akt1 中一个独特启动子的转录激活促进乳腺上皮细胞的存活。
Mol Cell Biol. 2010 Jun;30(12):2957-70. doi: 10.1128/MCB.00851-09. Epub 2010 Apr 12.
3
Stat5 promotes metastatic behavior of human prostate cancer cells in vitro and in vivo.Stat5 促进人前列腺癌细胞在体外和体内的转移行为。
Endocr Relat Cancer. 2010 May 18;17(2):481-93. doi: 10.1677/ERC-09-0328. Print 2010 Jun.
4
Transcription factor Stat3 stimulates metastatic behavior of human prostate cancer cells in vivo, whereas Stat5b has a preferential role in the promotion of prostate cancer cell viability and tumor growth.转录因子 Stat3 可刺激体内人前列腺癌细胞的转移行为,而 Stat5b 在促进前列腺癌细胞活力和肿瘤生长方面具有优先作用。
Am J Pathol. 2010 Apr;176(4):1959-72. doi: 10.2353/ajpath.2010.090653. Epub 2010 Feb 18.
5
The JAK2 inhibitor AZD1480 potently blocks Stat3 signaling and oncogenesis in solid tumors.JAK2抑制剂AZD1480可有效阻断实体瘤中的Stat3信号传导和肿瘤发生。
Cancer Cell. 2009 Dec 8;16(6):487-97. doi: 10.1016/j.ccr.2009.10.015.
6
Transcription factor Stat5a/b as a therapeutic target protein for prostate cancer.转录因子 Stat5a/b 作为前列腺癌的治疗靶标蛋白。
Int J Biochem Cell Biol. 2010 Feb;42(2):186-92. doi: 10.1016/j.biocel.2009.11.001. Epub 2009 Nov 13.
7
Signal transducer and activator of transcription 5A/B in prostate and breast cancers.前列腺癌和乳腺癌中的信号转导及转录激活因子5A/B
Endocr Relat Cancer. 2008 Jun;15(2):367-90. doi: 10.1677/ERC-08-0013.
8
Transcription factor signal transducer and activator of transcription 5 promotes growth of human prostate cancer cells in vivo.转录因子信号转导子和转录激活子5促进人前列腺癌细胞在体内的生长。
Clin Cancer Res. 2008 Mar 1;14(5):1317-24. doi: 10.1158/1078-0432.CCR-07-2024.
9
Transcription factor Stat5 synergizes with androgen receptor in prostate cancer cells.转录因子Stat5与前列腺癌细胞中的雄激素受体协同作用。
Cancer Res. 2008 Jan 1;68(1):236-48. doi: 10.1158/0008-5472.CAN-07-2972.
10
JAK2 inhibitor therapy in myeloproliferative disorders: rationale, preclinical studies and ongoing clinical trials.JAK2抑制剂治疗骨髓增殖性疾病:原理、临床前研究及正在进行的临床试验。
Leukemia. 2008 Jan;22(1):23-30. doi: 10.1038/sj.leu.2404948. Epub 2007 Sep 20.

信号转导子和转录激活子 5a/b:前列腺癌和乳腺癌的生物标志物和治疗靶点。

Signal transducer and activator of transcription 5a/b: biomarker and therapeutic target in prostate and breast cancer.

机构信息

Department of Cancer Biology, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, United States.

出版信息

Int J Biochem Cell Biol. 2011 Oct;43(10):1417-21. doi: 10.1016/j.biocel.2011.06.007. Epub 2011 Jun 17.

DOI:10.1016/j.biocel.2011.06.007
PMID:21704724
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3163765/
Abstract

The search for new therapeutic strategies for prostate and breast cancer is of significant interest. Signal transducer and activator of transcription 5a/b (Stat5a/b) controls viability and growth of prostate cancer. Nuclear active Stat5a/b expression is clustered to high grade prostate cancers, predicts early disease recurrence and promotes metastatic dissemination of prostate cancer. In breast cancer, the role of Stat5a/b is more complex. In rodent model systems, Stat5a/b may promote malignant transformation and enhance growth of the breast tumors. In contrast, Stat5a/b activation in established human breast cancer positively correlates with tumor differentiation, prevents metastatic dissemination, and predicts favorable clinical outcome of node-negative breast cancer. Here we review the molecular structure and biological functions of Stat5a/b and discuss the potential applications of Stat5a/b for therapy development and as a prognostic marker for prostate and breast cancer.

摘要

寻找前列腺癌和乳腺癌的新治疗策略具有重要意义。信号转导子和转录激活子 5a/b(Stat5a/b)控制前列腺癌的存活和生长。核活性 Stat5a/b 表达与高级别前列腺癌聚集,预测早期疾病复发并促进前列腺癌的转移扩散。在乳腺癌中,Stat5a/b 的作用更为复杂。在啮齿动物模型系统中,Stat5a/b 可能促进恶性转化并增强乳腺肿瘤的生长。相比之下,在已建立的人类乳腺癌中,Stat5a/b 的激活与肿瘤分化呈正相关,可防止转移扩散,并预测淋巴结阴性乳腺癌的良好临床结局。本文综述了 Stat5a/b 的分子结构和生物学功能,并讨论了 Stat5a/b 在治疗开发和作为前列腺癌和乳腺癌的预后标志物方面的潜在应用。