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癌症中转录信号转导子与激活子家族基因的突变

Mutations in the signal transducer and activator of transcription family of genes in cancer.

作者信息

Shahmarvand Nahid, Nagy Alexandra, Shahryari Jahanbanoo, Ohgami Robert S

机构信息

Department of Pathology, Stanford University, Stanford, CA, USA.

出版信息

Cancer Sci. 2018 Apr;109(4):926-933. doi: 10.1111/cas.13525. Epub 2018 Mar 2.

Abstract

In recent years, it has become clear that members of the signal transducer and activator of transcription (STAT) family of genes play an important role in cancer. The STAT family consists of seven genes, STAT1-4, STAT5A, STAT5B and STAT6, that are involved in regulating cellular proliferation, apoptosis, angiogenesis and the immune system response. Constitutive activation of STAT3, via mutational changes, is important in oncogenesis in both solid and hematopoietic cancers. In the case of hematopoietic neoplasms, STAT3 driver mutations have been described in T-cell large granular lymphocytic (T-LGL) leukemia and chronic natural killer lymphoproliferative disorders (CLPD-NK) and are seen in 30%-40% of T-LGL leukemia patients. STAT5B is also mutated in T-LGL leukemia and CLPD-NK, but in a much smaller proportion. Here we review past and current research on STAT genes in hematopoietic and solid cancers with emphasis on STAT3 and STAT5B and their roles in the pathogenesis of hematopoietic malignancies, particularly T-LGL leukemia and CLPD-NK.

摘要

近年来,信号转导子和转录激活子(STAT)基因家族成员在癌症中发挥重要作用已变得清晰。STAT家族由七个基因组成,即STAT1 - 4、STAT5A、STAT5B和STAT6,它们参与调节细胞增殖、凋亡、血管生成和免疫系统反应。通过突变变化导致的STAT3组成性激活在实体癌和血液系统癌症的肿瘤发生中都很重要。在血液系统肿瘤中,STAT3驱动突变已在T细胞大颗粒淋巴细胞(T - LGL)白血病和慢性自然杀伤细胞淋巴增殖性疾病(CLPD - NK)中被描述,并且在30% - 40%的T - LGL白血病患者中可见。STAT5B在T - LGL白血病和CLPD - NK中也发生突变,但比例要小得多。在此,我们回顾过去和当前关于血液系统癌症和实体癌中STAT基因的研究,重点是STAT3和STAT5B及其在血液系统恶性肿瘤,特别是T - LGL白血病和CLPD - NK发病机制中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f43/5891179/91f5e72aa061/CAS-109-926-g001.jpg

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