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前列腺癌和乳腺癌中的信号转导及转录激活因子5A/B

Signal transducer and activator of transcription 5A/B in prostate and breast cancers.

作者信息

Tan Shyh-Han, Nevalainen Marja T

机构信息

Department of Cancer Biology, Kimmel Cancer Center, Thomas Jefferson University, 233 South 10th Street, BLSB 309, Philadelphia, Pennsylvania 19107, USA.

出版信息

Endocr Relat Cancer. 2008 Jun;15(2):367-90. doi: 10.1677/ERC-08-0013.

DOI:10.1677/ERC-08-0013
PMID:18508994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6036917/
Abstract

Protein kinase signaling pathways, such as Janus kinase 2-Signal transducer and activator of transcription 5A/B (JAK2-STAT5A/B), are of significant interest in the search for new therapeutic strategies in both breast and prostate cancers. In prostate cancer, the components of the JAK2-STAT5A/B signaling pathway provide molecular targets for small-molecule inhibition of survival and growth signals of the cells. At the same time, new evidence suggests that the STAT5A/B signaling pathway is involved in the transition of organ-confined prostate cancer to hormone-refractory disease. This implies that the active JAK2-STAT5A/B signaling pathway potentially provides the means for pharmacological intervention of clinical prostate cancer progression. In addition, active STAT5A/B may serve as a prognostic marker for identification of those primary prostate cancers that are likely to progress to aggressive disease. In breast cancer, the role of STAT5A/B is more complex. STAT5A/B may have a dual role in the regulation of malignant mammary epithelium. Data accumulated from mouse models of breast cancer suggest that in early stages of breast cancer STAT5A/B may promote malignant transformation and enhance growth of the tumor. This is in contrast to established breast cancer, where STAT5A/B may mediate the critical cues for maintaining the differentiation of mammary epithelium. In addition, present data suggest that activation of STAT5A/B in breast cancer predicts favorable clinical outcome. The dual nature of STAT5A/B action in breast cancer makes the therapeutic use of STAT5 A/B more complex.

摘要

蛋白激酶信号通路,如Janus激酶2-信号转导子和转录激活子5A/B(JAK2-STAT5A/B),在寻找乳腺癌和前列腺癌新治疗策略方面备受关注。在前列腺癌中,JAK2-STAT5A/B信号通路的组成成分提供了小分子抑制细胞存活和生长信号的分子靶点。同时,新证据表明STAT5A/B信号通路参与了局限于器官的前列腺癌向激素难治性疾病的转变。这意味着活跃的JAK2-STAT5A/B信号通路可能为临床前列腺癌进展的药物干预提供了途径。此外,活跃的STAT5A/B可能作为一种预后标志物,用于识别那些可能进展为侵袭性疾病的原发性前列腺癌。在乳腺癌中,STAT5A/B的作用更为复杂。STAT5A/B在恶性乳腺上皮细胞的调控中可能具有双重作用。从乳腺癌小鼠模型积累的数据表明,在乳腺癌早期,STAT5A/B可能促进恶性转化并增强肿瘤生长。这与已确诊的乳腺癌情况相反,在已确诊的乳腺癌中,STAT5A/B可能介导维持乳腺上皮细胞分化的关键信号。此外,目前的数据表明,乳腺癌中STAT5A/B的激活预示着良好的临床结果。STAT5A/B在乳腺癌中的双重作用性质使得其治疗应用更为复杂。

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Cancer Res. 2008 Jan 1;68(1):236-48. doi: 10.1158/0008-5472.CAN-07-2972.
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Front Oncol. 2024 Mar 28;14:1354543. doi: 10.3389/fonc.2024.1354543. eCollection 2024.
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