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疾病机制:对转录信号转导子和激活子在癌症中新兴作用的见解。

Mechanisms of disease: Insights into the emerging role of signal transducers and activators of transcription in cancer.

作者信息

Haura Eric B, Turkson James, Jove Richard

机构信息

Thoracic Oncology Program, H Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.

出版信息

Nat Clin Pract Oncol. 2005 Jun;2(6):315-24. doi: 10.1038/ncponc0195.

Abstract

Members of the signal transducers and activators of transcription (STAT) pathway, which were originally identified as key components linking cytokine signals to transcriptional events in cells, have recently been demonstrated to have a major role in cancer. They are cytoplasmic proteins that form functional dimers with each other when activated by tyrosine phosphorylation. Activated STAT proteins translocate to the nucleus to regulate expression of genes by binding to specific elements within gene promoters. Constitutive activation of the STAT family members Stat3 and Stat5, and/or loss of Stat1 signaling, is found in a large group of diverse tumors. Increasing evidence demonstrates that STAT proteins can regulate many pathways important in oncogenesis including cell-cycle progression, apoptosis, tumor angiogenesis, tumor-cell invasion and metastasis, and tumor-cell evasion of the immune system. Based on these findings, a growing effort is underway to target STAT proteins directly and indirectly for cancer therapy. This review will highlight STAT signaling pathways, STAT target genes involved in cancer, evidence for STAT activation in human cancers, and therapeutic strategies to target STAT molecules for anticancer therapy.

摘要

信号转导与转录激活因子(STAT)通路的成员最初被确定为将细胞因子信号与细胞内转录事件联系起来的关键成分,最近已被证明在癌症中起主要作用。它们是细胞质蛋白,在被酪氨酸磷酸化激活时相互形成功能性二聚体。激活的STAT蛋白转移到细胞核,通过与基因启动子内的特定元件结合来调节基因表达。在一大类不同的肿瘤中发现STAT家族成员Stat3和Stat5的组成性激活和/或Stat1信号传导的丧失。越来越多的证据表明,STAT蛋白可以调节许多在肿瘤发生中重要的途径,包括细胞周期进程、细胞凋亡、肿瘤血管生成、肿瘤细胞侵袭和转移以及肿瘤细胞对免疫系统的逃避。基于这些发现,针对癌症治疗直接和间接靶向STAT蛋白的努力正在不断增加。本综述将重点介绍STAT信号通路、参与癌症的STAT靶基因、人类癌症中STAT激活的证据以及针对STAT分子进行抗癌治疗的策略。

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