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High-fat diet promotes prostate cancer metastasis via RPS27

Authors :
Dameng Li
Xueying Zhou
Wenxian Xu
Yongxin Cai
Chenglong Mu
Xinchun Zhao
Tingting Tang
Chen Liang
Tao Yang
Junnian Zheng
Liang Wei
Bo Ma
Source :
Cancer & Metabolism, Vol 12, Iss 1, Pp 1-11 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Abstract Background Metastasis is the leading cause of death among prostate cancer (PCa) patients. Obesity is associated with both PCa-specific and all-cause mortality. High-fat diet (HFD) is a risk factor contributing to obesity. However, the association of HFD with PCa metastasis and its underlying mechanisms are unclear. Methods Tumor xenografts were conducted by intrasplenic injections. The ability of migration or invasion was detected by transwell assay. The expression levels of RPS27 were detected by QRT-PCR and western blot. Results The present study verified the increase in PCa metastasis caused by HFD in mice. Bioinformatics analysis demonstrated increased RPS27 in the experimentally induced PCa in HFD mice, indicating that it is an unfavorable prognostic factor. Intrasplenic injections were used to demonstrate that RPS27 overexpression promotes, while RPS27 knockdown significantly reduces, PCa liver metastasis. Moreover, RPS27 inhibition suppresses the effects of HFD on PCa metastasis. Further mRNA sequencing analysis revealed that RPS27 promotes PCa metastasis by selectively enhancing the expression of various genes. Conclusion Our findings indicate that HFD increases the risk of PCa metastasis by elevating RPS27 expression and, subsequently, the expression of genes involved in PRAD progression. Therefore, RPS27 may serve as a novel target for the diagnosis and treatment of metastatic PCa.

Details

Language :
English
ISSN :
20493002
Volume :
12
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Cancer & Metabolism
Publication Type :
Academic Journal
Accession number :
edsdoj.beb4836389bd48a9a43c4a886d9b0d4c
Document Type :
article
Full Text :
https://doi.org/10.1186/s40170-024-00333-7