人类乳腺癌中的蛋白精氨酸甲基转移酶 CARM1。

IF 3.8 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Megan Bacabac, Peng Liu, Wei Xu
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引用次数: 0

摘要

共激活因子相关精氨酸甲基转移酶 1(CARM1)是一种蛋白质精氨酸甲基转移酶,可在组蛋白和非组蛋白底物上沉积不对称的二甲基化标记。CARM1 在转录中的调控作用最早是在雌激素受体阳性(ER+)乳腺癌中发现的。此后,人们进一步研究了 CARM1 激活 ER 靶基因的机制。在ER阴性(ER-)乳腺癌中,CARM1的表达水平最高,且较高的表达水平与预后不良相关,这表明CARM1具有致癌作用。 事实上,在ER-乳腺癌中,CARM1至少部分是通过甲基化蛋白和激活癌基因来促进增殖和转移的。在本综述中,我们将总结 CARM1 在乳腺癌中的转录激活机制。CARM1的甲基转移酶活性对它的许多功能都很重要,在此,我们还强调了CARM1的非酶作用。 我们还介绍了CARM1调控的、在癌症中经常失调的生物过程,以及在癌症治疗中利用CARM1的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protein Arginine Methyltransferase CARM1 in Human Breast Cancer.

Coactivator-associated arginine methyltransferase 1 (CARM1) is a protein arginine methyltransferase that deposits asymmetrical dimethylation marks on both histone and nonhistone substrates. The regulatory role of CARM1 in transcription was first identified in estrogen receptor positive (ER+) breast cancer. Since then, the mechanism of CARM1 in activating ER-target genes has been further interrogated. CARM1 is expressed at the highest level in ER negative (ER-) breast cancer and higher expression correlates with poor prognosis, suggesting an oncogenic role of CARM1. Indeed, in ER- breast cancer, CARM1 can promote proliferation and metastasis at least partly through methylation of proteins and activation of oncogenes. In this review, we summarize the mechanisms of transcriptional activation by CARM1 in breast cancer. The methyltransferase activity of CARM1 is important for many of its functions; here, we also highlight the nonenzymatic roles of CARM1. We also cover the biological processes regulated by CARM1 that are often deregulated in cancer and the ways to harness CARM1 in cancer treatment.

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来源期刊
Endocrinology
Endocrinology 医学-内分泌学与代谢
CiteScore
8.10
自引率
4.20%
发文量
195
审稿时长
2-3 weeks
期刊介绍: The mission of Endocrinology is to be the authoritative source of emerging hormone science and to disseminate that new knowledge to scientists, clinicians, and the public in a way that will enable "hormone science to health." Endocrinology welcomes the submission of original research investigating endocrine systems and diseases at all levels of biological organization, incorporating molecular mechanistic studies, such as hormone-receptor interactions, in all areas of endocrinology, as well as cross-disciplinary and integrative studies. The editors of Endocrinology encourage the submission of research in emerging areas not traditionally recognized as endocrinology or metabolism in addition to the following traditionally recognized fields: Adrenal; Bone Health and Osteoporosis; Cardiovascular Endocrinology; Diabetes; Endocrine-Disrupting Chemicals; Endocrine Neoplasia and Cancer; Growth; Neuroendocrinology; Nuclear Receptors and Their Ligands; Obesity; Reproductive Endocrinology; Signaling Pathways; and Thyroid.
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