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长链非编码RNA CKMT2-AS1通过靶向AKT/mTOR信号通路降低结肠癌细胞的活力。

Long Non-Coding RNA CKMT2-AS1 Reduces the Viability of Colorectal Cancer Cells by Targeting AKT/mTOR Signaling Pathway.

作者信息

Zhuang Biao, Ni Xiong, Min Zhijun, Wu Dejun, Wang Tingfeng, Cui Peng

机构信息

Department of General Surgery, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai 201399, China.

出版信息

Iran J Public Health. 2022 Feb;51(2):327-335. doi: 10.18502/ijph.v51i2.8685.

Abstract

BACKGROUND

Colorectal cancer (CRC) has not only seriously affected people's lives, but also burdened the government healthcare system. Long non-coding RNAs (lncRNA) have attracted more and more attention in the cancer study field.

METHODS

Experiments were completed in the Medical Research and Innovation Center of Shanghai Pudong Hospital, China from 2019 to 2020. Cell cycle was detected by western blot analyzing and flow cytometry. Apoptosis analysis were determined using flow cytometry or western blot analysis. LncRNA was knocked down by shRNA transfection.

RESULTS

We found was the most significant=0.0105 for SW480 and =0.0071 for HCT116) difference lncRNA between colorectal cancer treated with autophagy inducer and colorectal cancer without any treatment. Effective shRNA- was also designed. Following, we found the treatment of autophagy inducer and autophagy inducer + shRNA-NC were able to suppress the proliferation of both SW480 and HCT116 cells. In addition, the treatment of autophagy inducer + shRNA- significantly reduced the apoptosis of SW480 and HCT116 cells induced by autophagy. Furthermore, we found the phosphorylation of mTOR, AKT was enhanced in SW480, and HCT116 cells treated with autophagy inducer + shRNA- compared to the cells treated with autophagy inducer of autophagy inducer + shRNA-NC.

CONCLUSION

Enhancing the expression of will become a promising strategy to prevent the progress of colorectal cancer.

摘要

背景

结直肠癌(CRC)不仅严重影响人们的生活,还给政府医疗保健系统带来负担。长链非编码RNA(lncRNA)在癌症研究领域越来越受到关注。

方法

实验于2019年至2020年在中国上海浦东医院医学研究与创新中心完成。通过蛋白质免疫印迹分析和流式细胞术检测细胞周期。使用流式细胞术或蛋白质免疫印迹分析进行细胞凋亡分析。通过shRNA转染敲低LncRNA。

结果

我们发现,在用自噬诱导剂治疗的结直肠癌与未进行任何治疗的结直肠癌之间,[具体lncRNA名称未给出]是差异最显著的lncRNA(对SW480而言,[具体数值未给出] = 0.0105;对HCT116而言,[具体数值未给出] = 0.0071)。还设计了有效的shRNA - [具体名称未给出]。随后,我们发现自噬诱导剂以及自噬诱导剂 + shRNA - NC的处理能够抑制SW480和HCT116细胞的增殖。此外,自噬诱导剂 + shRNA - [具体名称未给出]的处理显著降低了自噬诱导的SW480和HCT116细胞的凋亡。此外,我们发现与用自噬诱导剂或自噬诱导剂 + shRNA - NC处理的细胞相比,用自噬诱导剂 + shRNA - [具体名称未给出]处理的SW480和HCT116细胞中mTOR、AKT的磷酸化增强。

结论

增强[具体lncRNA名称未给出]的表达将成为预防结直肠癌进展的一种有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f9/9273497/5fcdd00dafd0/IJPH-51-327-g001.jpg

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