Suppr超能文献

肌动蛋白结合蛋白膜突蛋白促进小鼠肝细胞癌的进展。

Actin-binding protein anillin promotes the progression of hepatocellular carcinoma and in mice.

作者信息

Jia Huanxia, Gao Zhenya, Yu Fang, Guo Hongfang, Li Baoyu

机构信息

School of Medicine, Xuchang University, Xuchang, Henan 461000, P.R. China.

Department of General Surgery, The Secondary Hospital of Tianjin Medical University, Tianjin 300211, P.R. China.

出版信息

Exp Ther Med. 2021 May;21(5):454. doi: 10.3892/etm.2021.9885. Epub 2021 Mar 1.

Abstract

Hepatocellular carcinoma (HCC) is a common type of tumor with high mortality worldwide. Investigations associated with the molecular etiology of HCC and screening novel therapeutic targets are still urgently in need. Anillin (ANLN), as a type of evolutionarily conserved actin-binding protein, is involved in multiple cellular processes. ANLN widely affected the progression and metastasis of several types of cancer, and its overexpression was frequently demonstrated in previous studies. The present study demonstrated high expression of ANLN in human HCC tissues, which was also associated the prognosis of patients with HCC. The associations between ANLN expression and the clinicopathological features were determined, including the number of tumor nodes (P=0.011) and tumor size (P=0.003) of patients with HCC. It was found that ANLN promoted cell proliferation, invasion and migration of HCC cells , and affected tumor growth . Therefore, ANLN is suggested as a promising therapeutic target for the treatment of HCC.

摘要

肝细胞癌(HCC)是一种在全球范围内死亡率很高的常见肿瘤类型。与HCC分子病因相关的研究以及筛选新的治疗靶点仍然迫切需要。膜收缩蛋白(ANLN)作为一种进化上保守的肌动蛋白结合蛋白,参与多种细胞过程。ANLN广泛影响多种类型癌症的进展和转移,并且在先前的研究中经常证明其过表达。本研究证明ANLN在人HCC组织中高表达,这也与HCC患者的预后相关。确定了ANLN表达与临床病理特征之间的关联,包括HCC患者的肿瘤结节数量(P = 0.011)和肿瘤大小(P = 0.003)。发现ANLN促进HCC细胞的增殖、侵袭和迁移,并影响肿瘤生长。因此,ANLN被认为是治疗HCC的一个有前景的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed43/7967816/9ee36784c566/etm-21-05-09885-g00.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验