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 Endourology(Electronic Edition) ›› 2022, Vol. 16 ›› Issue (03): 262-269. doi: 10.3877/cma.j.issn.1674-3253.2022.03.016

• Experiment Research • Previous Articles     Next Articles

ASF1B enhances the migration and proliferation of prostate cancers via regulating p53-related signaling pathways

Zhen Lei1, Zhenghui Guo1, Chen Tang1, Shengmeng Peng1, Yanting Ren2, Wanhua Wu1, Jie Zhou1, Yongming Chen1, Lingfeng Li1, Hai Huang1, Yiming Lai1,()   

  1. 1. Department of Urology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China; Guangdong Provincial Clinical Research Center for Urological Diseases, Guangzhou 510120, China; Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China
    2. Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China; Department of Pathology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China
  • Received:2022-01-04 Online:2022-06-01 Published:2022-05-19
  • Contact: Yiming Lai

Abstract:

Objective

To study the effect of Anti-Silencing Function 1B Histone Chaperone (ASF1B) on the migration and proliferation of prostate cancer (PCa), and to explore the specific molecular mechanism of ASF1B regulating P53-related signal pathway.

Methods

The survival and prognosis of ASF1B in prostate cancer patients was analyzed according to the data in TCGA database. After the expression of ASF1B was knocked down by small interference RNA (SiRNA), the mobility of cells was compared by Transwell cell migration test, the ability of cell proliferation was compared by CCK8 test and plate cloning test, and the apoptosis rate was compared by apoptosis test. The changes of signal pathways after ASF1B knockout were compared by transcriptome second generation sequencing, and the changes of protein and mRNA levels of P53 related signal pathway molecules were compared by Western-Blot test and Q-PCR test, in order to clarify the effect of ASF1B on the migration and proliferation of prostate cancer cells.

Results

After SiRNA knocked down the expression of ASF1B, the motor ability of DU145 and PC3 cells decreased, and the number of cells passing through the chamber decreased at the same time. After knocking down the expression of ASF1B, the number and size of cell viability and colony formation of DU145 and PC3 cells decreased, and the ability of cell proliferation decreased. After knocking down the expression of ASF1B, the percentage of apoptosis of DU145 and PC3 cells increased. After knocking down the expression of ASF1B, the second generation sequencing results of transcriptional group of PC3 cells showed that the P53 signal pathway was regulated. After knocking down the expression of ASF1B, the expression of p21, IGFBP3 and BBC3 of P53-related pathways in PC3 cells increased, while the expression of Cyclin D, Snail and Slug decreased.

Conclusion

ASF1B regulates the migration and proliferation of prostate cancer cells through P53-related signaling pathways in a P53-independent manner. ASF1B is expected to be a new target for the diagnosis and treatment of prostate cancer.

Key words: Prostate cancer, Anti-Silencing Function 1B Histone Chaperone, P53 signaling pathway, Cell migration, Cell proliferation

京ICP 备07035254号-20
Copyright © Chinese Journal of Endourology(Electronic Edition), All Rights Reserved.
Tel: 020-85252990 E-mail: chinendourology@126.com
Powered by Beijing Magtech Co. Ltd