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HMGN5:胶质瘤中的一个潜在癌基因。

HMGN5: a potential oncogene in gliomas.

机构信息

Department of Neurosurgery, Shanghai Institute of Neurosurgery, Changzheng Hospital, Second Military Medical University, Shanghai, 200433, China.

出版信息

J Neurooncol. 2011 Sep;104(3):729-36. doi: 10.1007/s11060-011-0558-9. Epub 2011 Mar 4.

Abstract

Gliomas are the most common primary brain tumors in the central nervous system and a leading cause of tumor-related death. High-mobility group nucleosome binding domain 5 (HMGN5/NSBP1), which is highly expressed in breast cancer and in hormone-induced mouse uterine adenocarcinoma, acts as a potential oncogene in gliomas. In this study, the role of HMGN5 in the proliferation of human glioma cells was investigated by lentivirus-mediated RNA interference (RNAi). The decrease in HMGN5 expression in human glioma U251 and U87 cells caused cell cycle arrest in the G1 phase and a delay in cell proliferation, as well as resulting in more apoptosis and an inhibition of clonogenic growth in soft agar in U251 cells; these results suggest that HMGN5 is required for tumorigenesis in vitro. Furthermore, HMGN5 was highly expressed in both high-grade and low-grade glioma tissue samples compared with normal brain tissues. Collectively, our data suggest that HMGN5 may play a critical role in the development of gliomas.

摘要

神经胶质瘤是中枢神经系统中最常见的原发性脑肿瘤,也是肿瘤相关死亡的主要原因。高迁移率族核小体结合域 5(HMGN5/NSBP1)在乳腺癌和激素诱导的小鼠子宫腺癌中高度表达,在神经胶质瘤中作为一种潜在的癌基因。在这项研究中,通过慢病毒介导的 RNA 干扰(RNAi)研究了 HMGN5 在人神经胶质瘤细胞增殖中的作用。人神经胶质瘤 U251 和 U87 细胞中 HMGN5 表达的降低导致细胞周期停滞在 G1 期,并延迟细胞增殖,导致更多的细胞凋亡,并抑制 U251 细胞在软琼脂中的集落形成生长;这些结果表明 HMGN5 是体外肿瘤发生所必需的。此外,与正常脑组织相比,HMGN5 在高级别和低级别神经胶质瘤组织样本中高度表达。总之,我们的数据表明 HMGN5 可能在神经胶质瘤的发展中起关键作用。

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