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一种PTEN-COL17A1融合基因及其在Ⅶ型胶原蛋白表达和胶质母细胞瘤恶性程度中的新调控作用。

A PTEN-COL17A1 fusion gene and its novel regulatory role in Collagen XVII expression and GBM malignance.

作者信息

Yan Xiaoyan, Zhang Chuanbao, Liang Tingyu, Yang Fan, Wang Haoyuan, Wu Fan, Wang Wen, Wang Zheng, Cheng Wen, Xu Jiangnan, Jiang Tao, Chen Jing, Ding Yaozhong

机构信息

Department of Immunology, School of Basic Medical Sciences, Capital Medical University, Beijing 100069, China.

Beijing Neurosurgical Institute, Capital Medical University, Beijing 100050, China.

出版信息

Oncotarget. 2017 Aug 24;8(49):85794-85803. doi: 10.18632/oncotarget.20526. eCollection 2017 Oct 17.

Abstract

Collagen XVII expression has recently been demonstrated to be correlated with the tumor malignance. While Collagen XVII is known to be widely distributed in neurons of the human brain, its precise role in pathogenesis of glioblastoma multiforme (GBM) is unknown. In this study, we identified and characterized a new PTEN-COL17A1 fusion gene in GMB using transcriptome sequencing. Although fusion gene did not result in measurable fusion protein production, its presence is accompanied with high levels of COL17A1 expression, revealed a novel regulatory mechanism of Collagen XVII expression by PTEN-COL17A1 gene fusion. Knocked down Collagen XVII expression in glioma cell lines resulted in decreased tumor invasiveness, along with significant reduction of MMP9 expression, while increased Collagen XVII expression promotes invasive activities of glioma cells and associated with GBM recurrences. Together, our results uncovered a new PTEN-COL17A1 fusion gene and its novel regulatory role in Collagen XVII expression and GBM malignance, and demonstrated that COL17A1 could serve as a useful prognostic biomarker and therapeutic targets for GBM.

摘要

最近已证明胶原蛋白 XVII 的表达与肿瘤恶性程度相关。虽然已知胶原蛋白 XVII 广泛分布于人类大脑的神经元中,但其在多形性胶质母细胞瘤(GBM)发病机制中的精确作用尚不清楚。在本研究中,我们使用转录组测序在 GBM 中鉴定并表征了一种新的 PTEN - COL17A1 融合基因。尽管融合基因未导致可测量的融合蛋白产生,但其存在伴随着高水平的 COL17A1 表达,揭示了 PTEN - COL17A1 基因融合对胶原蛋白 XVII 表达的一种新的调控机制。在胶质瘤细胞系中敲低胶原蛋白 XVII 的表达导致肿瘤侵袭性降低,同时 MMP9 表达显著减少,而增加胶原蛋白 XVII 的表达则促进胶质瘤细胞的侵袭活性并与 GBM 复发相关。总之,我们的结果揭示了一种新的 PTEN - COL17A1 融合基因及其在胶原蛋白 XVII 表达和 GBM 恶性程度中的新调控作用,并证明 COL17A1 可作为 GBM 的有用预后生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09fb/5689647/aeca829fb13f/oncotarget-08-85794-g001.jpg

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