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核心蛋白聚糖基因的过表达影响甲状腺滤泡癌细胞的生物学行为。

Overexpression of decorin gene influences the biological behaviors of follicular thyroid carcinoma cells.

作者信息

Lin Qianhuang, Ma Ye, Guo Runsheng, Guo Hailong, Wang Xiaoyun, Yang Ting

机构信息

Department of General Surgery, Jiading District Central Hospital Affiliated Shanghai University of Medicine and Health Sciences, Shanghai 201800, P.R. China.

出版信息

Oncol Lett. 2025 Jun 2;30(2):374. doi: 10.3892/ol.2025.15120. eCollection 2025 Aug.

Abstract

The objective of the present study was to examine the impact of decorin (DCN) gene overexpression on the proliferation, migration and invasion of human follicular thyroid carcinoma (FTC) cells. DCN expression was evaluated by western blotting (WB) in Nthy-ori3-1 normal thyroid cells and in two FTC cell lines, namely FTC-133 and FTC-238. Lentiviral transfection was employed to overexpress DCN in the FTC cells, with the overexpression efficiency confirmed through reverse transcription-quantitative polymerase chain reaction and WB. Cell viability, colony formation, wound healing and Transwell invasion assays were conducted to assess the proliferation, migration and invasion of the transfected cells. The results revealed that DCN expression in FTC-133 and FTC-238 cells was significantly lower compared with that in Nthy-ori3-1 cells. Successful lentiviral overexpression of DCN in the FTC cell lines significantly decreased the proliferation and colony formation abilities of the cells, and diminished their wound healing and invasive capabilities. This indicated that the lentivirus-mediated overexpression of DCN in FTC-133 and FTC-238 cells altered their cellular behavior, providing experimental evidence to support the suggestion that DCN is a potential therapeutic target for FTC.

摘要

本研究的目的是检测核心蛋白聚糖(DCN)基因过表达对人甲状腺滤泡癌(FTC)细胞增殖、迁移和侵袭的影响。通过蛋白质免疫印迹法(WB)评估DCN在Nthy-ori3-1正常甲状腺细胞以及两种FTC细胞系(即FTC-133和FTC-238)中的表达。采用慢病毒转染使FTC细胞中DCN过表达,并通过逆转录-定量聚合酶链反应和WB确认过表达效率。进行细胞活力、集落形成、伤口愈合和Transwell侵袭试验,以评估转染细胞的增殖、迁移和侵袭能力。结果显示,与Nthy-ori3-1细胞相比,FTC-133和FTC-238细胞中DCN的表达显著降低。FTC细胞系中成功实现慢病毒介导的DCN过表达后,显著降低了细胞的增殖和集落形成能力,并减弱了其伤口愈合和侵袭能力。这表明慢病毒介导的DCN在FTC-133和FTC-238细胞中的过表达改变了它们的细胞行为,为支持DCN是FTC潜在治疗靶点这一观点提供了实验证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ffd/12150200/d916a67a4506/ol-30-02-15120-g00.jpg

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