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FAM72、多形性胶质母细胞瘤及其他相关疾病

FAM72, Glioblastoma Multiforme (GBM) and Beyond.

作者信息

Ho Nguyen Thi Thanh, Rahane Chinmay Satish, Pramanik Subrata, Kim Pok-Son, Kutzner Arne, Heese Klaus

机构信息

Graduate School of Biomedical Science and Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791, Korea.

Maharashtra Institute of Medical Education and Research, Talegaon Dabhade, Maharashtra 410507, India.

出版信息

Cancers (Basel). 2021 Mar 1;13(5):1025. doi: 10.3390/cancers13051025.

Abstract

Neural stem cells (NSCs) offer great potential for regenerative medicine due to their excellent ability to differentiate into various specialized cell types of the brain. In the central nervous system (CNS), NSC renewal and differentiation are under strict control by the regulation of the pivotal SLIT-ROBO Rho GTPase activating protein 2 (SRGAP2)-Family with sequence similarity 72 (FAM72) master gene (i.e., |-SRGAP2-FAM72-|) via a divergent gene transcription activation mechanism. If the gene transcription control unit (i.e., the intergenic region of the two sub-gene units, SRGAP2 and FAM72) gets out of control, NSCs may transform into cancer stem cells and generate brain tumor cells responsible for brain cancer such as glioblastoma multiforme (GBM). Here, we discuss the surveillance of this |-SRGAP2-FAM72-| master gene and its role in GBM, and also in light of FAM72 for diagnosing various types of cancers outside of the CNS.

摘要

神经干细胞(NSCs)因其具有分化为大脑各种特化细胞类型的卓越能力,在再生医学中具有巨大潜力。在中枢神经系统(CNS)中,NSC的更新和分化通过关键的SLIT-ROBO Rho GTP酶激活蛋白2(SRGAP2)-序列相似性72家族(FAM72)主基因(即|-SRGAP2-FAM72-|)的调控,经由一种不同的基因转录激活机制受到严格控制。如果基因转录控制单元(即两个亚基因单元SRGAP2和FAM72的基因间区域)失控,NSCs可能转化为癌症干细胞并产生负责诸如多形性胶质母细胞瘤(GBM)等脑癌的脑肿瘤细胞。在此,我们讨论这种|-SRGAP2-FAM72-|主基因的监测及其在GBM中的作用,并且鉴于FAM72用于诊断CNS之外的各种类型癌症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5d9/7957592/9f4c6ddce48d/cancers-13-01025-g008.jpg

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