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在口腔癌侵袭过程中,蛋白酶受肌动蛋白丝交联蛋白调控。

Proteases are Modulated by Fascin in Oral Cancer Invasion.

作者信息

Lee Min Kyeong, Park Ji Hyeon, Gi Seol Hwa, Hwang Young Sun

机构信息

Department of Dental Hygiene, College of Health Science, Eulji University, Seongnam, Korea.

出版信息

J Cancer Prev. 2018 Sep;23(3):141-146. doi: 10.15430/JCP.2018.23.3.141. Epub 2018 Sep 30.

Abstract

BACKGROUND

Cancer invasion is a critical factor for survival and prognosis of patients with cancer. Identifying and targeting factors that influence cancer invasion are an important strategy to overcome cancer. In this study, we investigated the role of fascin known to be associated with cancer invasion.

METHODS

Fascin depletion was performed with lentiviral short hairpin RNA against fascin mRNA and stable cell line (Fascin) was established. Matrigel-Transwell invasion and three-dimensional (3D) culture system were used to observe fascin depletion effects. In order to observe the changes of protease secretion by fascin depleted cancer cells, protease antibody array was performed.

RESULTS

Fascin was highly expressed in invasive cancer cells. Fascin-depleted cells showed decreased cancer invasion in Matrigel-Transwell invasion and 3D culture system. In addition, inhibition of proteases secreation and decrease of intracellular proteases mRNA expression were observed in fascin deplete cells.

CONCLUSIONS

These results indicates that fascin is closely involved in proteases activity and cancer invasion. Therefore, fascin is a strategically important factor for controlling cancer invasion.

摘要

背景

癌症侵袭是影响癌症患者生存和预后的关键因素。识别并靶向影响癌症侵袭的因素是攻克癌症的重要策略。在本研究中,我们调查了已知与癌症侵袭相关的细丝蛋白的作用。

方法

利用针对细丝蛋白mRNA的慢病毒短发夹RNA进行细丝蛋白敲减,并建立稳定细胞系(细丝蛋白敲减细胞系)。采用基质胶-Transwell侵袭实验和三维(3D)培养系统观察细丝蛋白敲减的效果。为了观察细丝蛋白敲减的癌细胞中蛋白酶分泌的变化,进行了蛋白酶抗体芯片检测。

结果

细丝蛋白在侵袭性癌细胞中高表达。在基质胶-Transwell侵袭实验和3D培养系统中,细丝蛋白敲减的细胞显示出癌症侵袭能力下降。此外,在细丝蛋白敲减的细胞中观察到蛋白酶分泌受到抑制,细胞内蛋白酶mRNA表达降低。

结论

这些结果表明细丝蛋白与蛋白酶活性和癌症侵袭密切相关。因此,细丝蛋白是控制癌症侵袭的一个具有重要战略意义的因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61b4/6197847/7804611b3076/jcp-23-141f1.jpg

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