Home    中文  
 
  • Search
  • lucene Search
  • Citation
  • Fig/Tab
  • Adv Search
Just Accepted  |  Current Issue  |  Archive  |  Featured Articles  |  Most Read  |  Most Download  |  Most Cited

Chinese Journal of Colorectal Diseases(Electronic Edition) ›› 2021, Vol. 10 ›› Issue (03): 260-265. doi: 10.3877/cma.j.issn.2095-3224.2021.03.007

• Original Article • Previous Articles     Next Articles

Effect of RNA-binding protein with multiple splicing on colitis associated colon cancer

Xinhua Zhao1, Yiming Ma1, Longmei He1, Hongying Wang1,()   

  1. 1. State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China
  • Received:2021-02-23 Online:2021-06-25 Published:2021-07-14
  • Contact: Hongying Wang

Abstract:

Objective

To investigate the expression of RNA alternative splicing protein RBPMS in colitis associated colon cancer and its effect on the proliferation of colon cancer cells.

Methods

Colitis-associated colon cancer was induced by azoxymethane (AOM) and dextran sulfate sodium (DSS) in C57BL/6 mice. Mice of four different stages during the development of colon cancer were obtained (inflammatory recovery stage, mild dysplasia, Adenoma, Adenocarcinoma), and a control group was established without any treatment. RNA sequencing was performed in different stages of colon tissue. HCT116 cells were transfected with specific small interfering RNA (siRNA) using LipofectamineTM 2 000. The total protein was extracted 72 hours later, and the knock-down efficiency was measured by Western blot. The effect of RBPMS knockdown on cell proliferation and clone formation ability was examined by MTT and clone-forming assay. Cell cycle were measured by Flow cytometry.

Results

The RNA sequencing results showed that the expression level of RBPMS mRNA increased with the development of colitis associated colon cancer. The results showed that knocking down RBPMS significantly inhibited the proliferation and clone forming ability of tumor cells by inducing G0/G1 arrest.

Conclusion

RBPMS is overexpressed in colitis associated colon cancer tissue, and RBPMS knock down can inhibit the proliferation of HCT116 cells.

Key words: RBPMS, Proliferation, Colitis associated Colon cancer

京ICP 备07035254号-20
Copyright © Chinese Journal of Colorectal Diseases(Electronic Edition), All Rights Reserved.
Tel: 0086-010-87788026 E-mail: cjcd_editor@vip.163.com
Powered by Beijing Magtech Co. Ltd