期刊
BIOENGINEERED
卷 12, 期 1, 页码 5892-5903出版社
TAYLOR & FRANCIS INC
DOI: 10.1080/21655979.2021.1971035
关键词
Bladder cancer; g-protein-coupled receptor; rgs19; gsk1070916; cell cycle
资金
- National Natural Science Foundation of China [82060465]
- Natural Science Foundation of Jiangxi Province [20161BAB205258]
- Science and Technology Support Program of Education Department of Jiangxi Province [GJJ150052]
The study identified RGS19 as a potential therapeutic target gene in bladder cancer, which is overexpressed in a wide range of tumors and associated with poor prognosis. In cell models, shRGS19 was found to halt the cell cycle at a polyploid point. Further cell rescue experiments showed that the drug GSK1070916 could inhibit the effect of RGS19 in vitro.
Bladder cancer is one of the most severe genitourinary cancers, causing high morbidity worldwide. However, the underlying molecular mechanism is not clear, and it is urgent to find target genes for treatment. G-protein-coupled receptors are currently a target of high interest for drug design. Thus, we aimed to identify a target gene-related to G-protein-coupled receptors for therapy. We used The Cancer Genome Atlas (TCGA) and DepMap databases to obtain the expression and clinical data of RGS19. The results showed that RGS19 was overexpressed in a wide range of tumor, especially bladder cancer. We also explored its effect on various types of cancer. High expression of RGS19 was also shown to be significantly associated with poor prognosis. Cell models were constructed for cell cycle detection. shRGS19 can halt the cell cycle at a polyploid point. RGS19 is a G-protein-coupled receptor signaling pathway-related gene with a significant effect on survival. We chose RGS19 as a therapeutic target gene in bladder cancer. The drug GSK1070916 was found to inhibit the effect of RGS19 via cell rescue experiments in vitro.
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