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almost4years
Bioinformatic gene analysis for possible biomarkers and therapeutic targets of hypertension-related renal cell carcinoma. (PubMed, Transl Androl Urol)
We identified the differentially expressed genes (DEGs) of HN and RCC through analyzing Gene Expression Omnibus (GEO) datasets GSE99339, GSE99325, GSE53757 and GSE15641 by means of bioinformatics analysis, respectively...CRIP1 and ESRRG and their corresponding predicted miRNAs, especially hsa-miR-221-5p, hsa-miR-205-5p, hsa-miR-152-3p and hsa-miR-137 may be notably related to hypertension-related RCC. CRIP1 and ESRRG genes have great potential to become novel biomarkers and therapeutic targets concerning hypertension-related RCC.
Journal
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MIR221 (MicroRNA 221) • BCAT1 (Branched Chain Amino Acid Transaminase 1 ) • MIR205 (MicroRNA 205)
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GS-156
4years
Screening, identification and validation of CCND1 and PECAM1/CD31 for predicting prognosis in renal cell carcinoma patients. (PubMed, Aging (Albany NY))
In this study, three expression profile data sets (GSE15641, GSE16441 and GSE66270) were integrated to identify candidate genes that could elucidate functional pathways in ccRCC...In summary, integrated bioinformatics analysis identified candidate DEGs and pathways in ccRCC that could improve our understanding of the causes and underlying molecular events of ccRCC. These candidate genes and pathways could be therapeutic targets for ccRCC.
Clinical • Journal
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CCND1 (Cyclin D1) • CXCR4 (Chemokine (C-X-C motif) receptor 4) • ICAM1 (Intercellular adhesion molecule 1) • EGF (Epidermal growth factor) • CD31 (Platelet and endothelial cell adhesion molecule 1)
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GS-156
over4years
[VIRTUAL] Screening, identification and validation of CCND1 and PECAM1/CD31 in predicting prognosis for renal cell carcinoma patients (EAU-I 2020)
In summary, using integrated bioinformatics analysis, candidate DEGs and pathways in ccRCC that could improve our understanding of the causes and underlying molecular events of ccRCC, and these candidate genes and pathways could be therapeutic targets for ccRCC were identified.
Clinical
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CCND1 (Cyclin D1) • CXCR4 (Chemokine (C-X-C motif) receptor 4) • ICAM1 (Intercellular adhesion molecule 1) • EGF (Epidermal growth factor) • CD31 (Platelet and endothelial cell adhesion molecule 1)
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GS-156
over4years
Long non-coding RNA LINC00520 promotes the proliferation and metastasis of malignant melanoma by inducing the miR-125b-5p/EIF5A2 axis. (PubMed, J Exp Clin Cancer Res)
All results elucidated the role and molecular mechanism of LINC00520 in the malignant development of melanoma. LINC00520, a new oncogene in melanoma, maybe serve as a survival biomarkers or therapeutic target for melanoma patients.
Journal
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LINC00520 (Long Intergenic Non-Protein Coding RNA 520)
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LINC00520 expression
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GS-156
over4years
The genetic association between type 2 diabetic and hepatocellular carcinomas. (PubMed, Ann Transl Med)
In order to identify differentially expressed genes (DEGs) in T2DM and HCC, gene expression datasets for T2DM (GSE15653), HCC (GSE60502) and metformin-treated cells (GSE69850) were obtained from the Gene Expression Omnibus database repository. This study identified a number of genes that may play important roles in the association of T2DM and HCC, including four genes which may be the target of metformin treatment for diabetes and HCC. The specific mechanisms involved remain to be identified.
Journal
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CHEK1 (Checkpoint kinase 1) • CCNA2 (Cyclin A2) • CCNB1 (Cyclin B1) • RACGAP1 (Rac GTPase activating protein 1)
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metformin • GS-156