Integrative analysis of deoxyribonuclease 1-like 3 as a potential biomarker in renal cell carcinoma

dc.contributor.authorGe, Minghuan
dc.contributor.authorZhu, Hengcheng
dc.contributor.authorSong, Huajie
dc.contributor.authorSchmeusser, Benjamin N.
dc.contributor.authorNg, Keng Lim
dc.contributor.authorZeng, Yan
dc.contributor.authorLiu, Ting
dc.contributor.authorYang, Kang
dc.contributor.departmentUrology, School of Medicine
dc.date.accessioned2024-03-14T11:14:19Z
dc.date.available2024-03-14T11:14:19Z
dc.date.issued2023
dc.description.abstractBackground: Clear cell renal cell carcinoma (ccRCC), the most common subtype of renal cell carcinoma (RCC), is insensitive to radiotherapy and chemotherapy after surgery. Deoxyribonuclease 1-like 3 (DNASE1L3), an endonuclease that cleaves both membrane-encapsulated single- and double-stranded DNA, suppresses cell cycle progression, proliferation and metabolism in hepatocellular carcinoma cells. There is currently no established link between DNASE1L3 and RCC inhibition. We are gonging to explored the mechanism underlying the relationship between DNASEL1L3 and RCC. Methods: RNA sequencing data for RCC tissue and peritumoral tissue were downloaded from The Cancer Genome Atlas database and analyzed. The expression levels of DNASE1L3 in RCC and normal samples were verified using the Gene Expression Omnibus (GEO) database, Human Protein Atlas database and western blotting. The role and potential mechanism of DNASE1L3 were investigated by analysis of immune-related databases and wound healing, invasion, cell counting kit 8 and immunofluorescence assays. Results: We revealed that DNASE1L3 expression was downregulated in RCC group compared with control group [The Cancer Genome Atlas (TCGA): 7.98 vs. 10.87, P<0.001]. Meanwhile, DNASE1L3 expression correlated with the clinical characteristics of patients. Patients with low DNASE1L3 expression had worse survival (P<0.001) and larger (r=-0.32, P<0.001) and heavier tumors (r=-0.17, P<0.001). DNASE1L3 overexpression inhibited the proliferation (786-O: 0.135±0.014 vs. 0.322±0.027, P<0.001) and invasion (786-O: 1,479±134 vs. 832±67, P<0.05) of RCC cells. The expression of DNASE1L3 was significantly correlated with the tumor immune microenvironment and drug sensitivity in ccRCC. Moreover, the level of the key phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) signaling pathway protein P-AKT was decreased in the group of cells transfected with DNASE1L3. Conclusions: This study strongly suggest that DNASE1L3 may be a promising potential biomarker for the diagnosis and treatment of ccRCC patients.
dc.eprint.versionFinal published version
dc.identifier.citationGe M, Zhu H, Song H, et al. Integrative analysis of deoxyribonuclease 1-like 3 as a potential biomarker in renal cell carcinoma. Transl Androl Urol. 2023;12(8):1308-1320. doi:10.21037/tau-23-355
dc.identifier.urihttps://hdl.handle.net/1805/39241
dc.language.isoen_US
dc.publisherAME
dc.relation.isversionof10.21037/tau-23-355
dc.relation.journalTranslational Andrology and Urology
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourcePMC
dc.subjectDeoxyribonuclease 1-like 3 (DNASE1L3)
dc.subjectTumor immune
dc.subjectRenal cell carcinoma (RCC)
dc.subjectBioinformatics analysis
dc.titleIntegrative analysis of deoxyribonuclease 1-like 3 as a potential biomarker in renal cell carcinoma
dc.typeArticle
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