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Deciphering the oncogenic potential of ADAM9 in hepatocellular carcinoma through bioinformatics and experimental approaches.
- Source :
-
Scientific reports [Sci Rep] 2024 Nov 02; Vol. 14 (1), pp. 26432. Date of Electronic Publication: 2024 Nov 02. - Publication Year :
- 2024
-
Abstract
- Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality worldwide. This study investigates the role and mechanisms of ADAM9 as a biomarker and potential therapeutic target in HCC. Utilizing RNA-sequencing data and clinicopathological characteristics from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases, we conducted survival and meta-analyses, functional enrichment, and immune infiltration studies. Additionally, we evaluated the effects of ADAM9 silencing on HCC cell proliferation, migration, and invasion through in vitro experiments. Our results demonstrate that high ADAM9 expression is associated with poor prognosis and increased immune infiltration in HCC patients. Furthermore, ADAM9 knockdown significantly inhibited tumor cell proliferation and migration. These findings indicate that ADAM9 is a promising prognostic biomarker and potential therapeutic target in HCC. In conclusion, ADAM9 could offer avenues for developing strategies to inhibit tumor progression and improve patient outcomes.<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Cell Line, Tumor
Cell Movement genetics
Prognosis
Biomarkers, Tumor genetics
Biomarkers, Tumor metabolism
Carcinoma, Hepatocellular genetics
Carcinoma, Hepatocellular pathology
Carcinoma, Hepatocellular metabolism
Liver Neoplasms genetics
Liver Neoplasms pathology
Liver Neoplasms metabolism
ADAM Proteins genetics
ADAM Proteins metabolism
Membrane Proteins genetics
Membrane Proteins metabolism
Computational Biology methods
Cell Proliferation genetics
Gene Expression Regulation, Neoplastic
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 14
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 39488509
- Full Text :
- https://doi.org/10.1038/s41598-024-74650-8