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CXCL2 的过表达抑制肝癌细胞增殖并促进其凋亡。

Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma.

机构信息

Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery First Affiliated Hospital School of Medicine, Zhejiang University; Key Laboratory of Combined Multi-organ Transplantation, Ministry of Public Health; Key Laboratory of the Diagnosis and Treatment of Organ Transplantation, Chinese Academy of Medical Sciences; Key Laboratory of Organ Transplantation, Hangzhou, Zhejiang 310003, P.R.China.

Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery First Affiliated Hospital School of Medicine, Zhejiang University; Department of Hepatobiliary Surgical, First Hospital of Jiaxing, Jiaxing, Zhejiang 314000, P.R.China.

出版信息

BMB Rep. 2018 Dec;51(12):630-635. doi: 10.5483/BMBRep.2018.51.12.140.

Abstract

C-X-C motif chemokine ligand 2 (CXCL2) is a small secreted protein that exhibits a structure similar to the proangiogenic subgroup of the CXC chemokine family. Recently, accumulating evidence suggests that chemokines play a pivotal role in cancer progression and carcinogenesis. We examined the expression levels of 7 types of ELR+ CXCLs messenger RNA (mRNA) in 264 clinical samples. We found that CXCL2 expression was stably down-regulated in 94% of hepatocellular carcinoma (HCC) specimens compared with paired adjacent normal liver tissues and some HCC cell lines. Moreover, CXCL2 overexpression profoundly attenuated HCC cell proliferation and growth and induced apoptosis in vitro. In animal studies, we found that overexpressing CXCL2 by lentivirus also apparently inhibited the size and weight of subcutaneous tumours in nude mice. Furthermore, we demonstrated that CXCL2 induced HCC cell apoptosis via both nuclear and mitochondrial apoptosis pathways. Our results indicate that CXCL2 negatively regulates the cell cycle in HCC cells via the ERK1/2 signalling pathway. These results provide new insights into HCC and may ultimately lead to the discovery of innovative therapeutic approaches of HCC. [BMB Reports 2018; 51(12): 630-635].

摘要

C-X-C 基序趋化因子配体 2(CXCL2)是一种小分泌蛋白,其结构与 CXC 趋化因子家族的促血管生成亚组相似。最近,越来越多的证据表明趋化因子在癌症进展和致癌作用中起关键作用。我们检查了 264 个临床样本中 7 种 ELR + CXCLs 信使 RNA(mRNA)的表达水平。我们发现,与配对的相邻正常肝组织和一些 HCC 细胞系相比,94%的肝细胞癌(HCC)标本中 CXCL2 的表达稳定下调。此外,CXCL2 的过表达可显著抑制 HCC 细胞的增殖和生长,并在体外诱导细胞凋亡。在动物研究中,我们发现通过慢病毒过表达 CXCL2 也明显抑制了裸鼠皮下肿瘤的大小和重量。此外,我们证明 CXCL2 通过核和线粒体凋亡途径诱导 HCC 细胞凋亡。我们的结果表明,CXCL2 通过 ERK1/2 信号通路负调控 HCC 细胞的细胞周期。这些结果为 HCC 提供了新的见解,并可能最终导致发现 HCC 的创新治疗方法。[BMB 报告 2018;51(12):630-635]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2863/6330937/64a0f5f67457/bmb-51-630f1.jpg

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