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Identification and validation of key miRNAs and a microRNA-mRNA regulatory network associated with liver cancer.
Tang, Jie; Li, Song; Zhou, Zixiao; Chang, Weicai; Wang, Yongqiang; Mei, Juan; Zhou, Shaobo.
Afiliação
  • Tang J; General Surgery, The Second Affiliated Hospital of Bengbu Medical College, Bengbu, China.
  • Li S; Anhui Key Laboratory of Tissue Transplantation, Bengbu Medical College, Bengbu, China.
  • Zhou Z; Department of Hepatobiliary pancreatic gastrointestinal Surgery, JinHua People's Hospital, JinHua, China.
  • Chang W; Xiangya Medical College, Central South University, Changsha, China.
  • Wang Y; Anhui Key Laboratory of Tissue Transplantation, Bengbu Medical College, Bengbu, China.
  • Mei J; General Surgery, The Second Affiliated Hospital of Bengbu Medical College, Bengbu, China.
  • Zhou S; Pathology Department, The Second Affiliated Hospital of Bengbu Medical College, Bengbu, China.
Cell Cycle ; 23(4): 353-368, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38547309
ABSTRACT
MiRNAs play crucial regulatory roles in the growth and development of tumor cells by serving as carriers of post-transcriptional regulatory information derived from genes. Investigating the potential function and clinical significance of miRNA-mediated mRNA regulatory networks in liver cancer can offer novel insights and therapeutic strategies for the treatment of this disease. We identified 300 differentially expressed miRNAs, and five miRNAs were identified to be correlated with overall survival and could be used as an independent prognostic. GO enrichment analysis mainly included carboxylic acid biosynthesis, organic acid biosynthesis, peroxisomal membrane, microsomal membrane, DNA binding, C-acyltransferase activity, etc. KEGG enrichment analysis showed that the pathways of target genes related to liver cancer were mainly focused on butyric acid metabolism and partial amino acid metabolism. Eight of the top 10 HUB genes were associated with prognosis, and the expression of four genes was positively correlated with prognosis, of which ABAT, BHMT, and SHMT1 were target genes of hsa-miR-5003-3p. MiR-5003-3p inhibits ABAT/BHMT/SHMT1 expression, thereby promoting liver cancer development. Overall, our study provides new ideas for the treatment of liver cancer, and these five miRNAs may be independent prognostic biomarkers and therapeutic targets for liver cancer patients. And miR-5003-3p may be a critical factor in the mechanism of liver cancer development.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Mensageiro / Regulação Neoplásica da Expressão Gênica / MicroRNAs / Redes Reguladoras de Genes / Neoplasias Hepáticas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Mensageiro / Regulação Neoplásica da Expressão Gênica / MicroRNAs / Redes Reguladoras de Genes / Neoplasias Hepáticas Idioma: En Ano de publicação: 2024 Tipo de documento: Article