摘要
SET(SE易位,SET)是在各种人体组织中广泛表达的进化保守基因,特别是在性腺和神经系统中。作为多任务蛋白质,SET涉及必需的细胞过程,例如组蛋白修饰,染色质重塑,DNA修复,基因转录和雄激素合成。最近的研究表明,SET在乳腺癌,卵巢癌和各种其他恶性肿瘤中过表达。 SET表达水平与卵巢癌患者生存率和SET介导的雄激素合成活化之间的强相关性强烈表明,该因子可能在妇科癌症中起重要作用。在这里,我们总结了关于SET在肿瘤发生和癌症进展中的病理学意义的数据。我们分析了如何通过PP2A依赖和不依赖于PP2A途径的SET可以调节不同的细胞功能。还讨论了这些途径之间的潜在相互作用以及对SET的致癌活性的未来研究。
关键词: SET,PP2A,I2PP2A,INHAT,妇科癌症,类固醇激素,组蛋白伴侣。
图形摘要
Current Drug Targets
Title:Oncogenic Role of SET/I2PP2A for Gynecologic Cancers
Volume: 18 Issue: 10
关键词: SET,PP2A,I2PP2A,INHAT,妇科癌症,类固醇激素,组蛋白伴侣。
摘要: SET (SE translocation, SET) is an evolutionarily conserved gene broadly expressed in various human tissues, especially in the gonadal and neural system. As a multitasking protein, SET is involved in essential cell processes such as histone modification, chromatin remodeling, DNA repair, gene transcription, and androgen synthesis. Recent studies showed that SET is overexpressed in breast cancers, ovary cancers and a variety of other malignancies. The strong correlation between SET expression levels and survival of ovarian cancer patients, and SET-mediated activation of androgen synthesis, strongly indicated that this factor may play a significant role in gynecologic cancers. Here, we summarized data pertaining to the pathological implications of SET in tumorigenesis and cancer progression. We analyzed how SET, through the PP2A-dependent and PP2A-independent pathways, may regulate different cell functions. Potential interactions among these pathways and future studies on SET’s oncogenic activities are also discussed.
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Cite this article as:
Oncogenic Role of SET/I2PP2A for Gynecologic Cancers, Current Drug Targets 2017; 18 (10) . https://dx.doi.org/10.2174/1389450118666170328114506
DOI https://dx.doi.org/10.2174/1389450118666170328114506 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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