Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0345904 (
liver cancer
)
15,188
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
This study aimed to evaluate the correlation of
integrin alpha 7
(
ITGA7
) with clinical outcomes and its effect on cell activities as well as stemness in hepatocellular carcinoma (HCC). HCC tumor tissues and paired adjacent tissues from 90 HCC patients were obtained and
ITGA7
expression was detected using immunohistochemistry assay. Cellular experiments were conducted to examine the effect of
ITGA7
on cell activities, astemness via
ITGA7
ShRNA transfection, and compensation experiments were further performed to test whether
ITGA7
functioned via regulating PTK2-PI3K-AKT signaling pathway.
ITGA7
was overexpressed in tumor tissues compared with paired adjacent tissues and its high expression was correlated with larger tumor size, vein invasion and advanced Barcelona Clinic
Liver Cancer
stage, and it also independently predicted worse overall survival in HCC patients. In cellular experiments,
ITGA7
was upregulated in SMMC-7721, Hep G2, HuH-7 and BEL-7404 cell lines compared with normal human liver cells HL-7702.
ITGA7
knockdown suppressed cell proliferation but promoted apoptosis, and it also downregulated CSCs markers (CD44, CD133 and OCT-4) as well as PTK2, PI3K and AKT expressions in SMMC-7721 and Hep G2 cell lines.
ITGA7
overexpression promoted cell proliferation but inhibited apoptosis, and it also upregulated CSCs markers in HL-7702 cells. Further compensation experiments verified that
ITGA7
regulated cell proliferation, apoptosis and CSCs markers via PTK2-PI3K-Akt signaling pathway.
ITGA7
negatively associates with clinical outcomes in HCC patients, and it regulates cell proliferation, apoptosis and CSCs markers via PTK2-PI3K-Akt signaling pathway.
...
PMID:Integrin alpha 7 correlates with poor clinical outcomes, and it regulates cell proliferation, apoptosis and stemness via PTK2-PI3K-Akt signaling pathway in hepatocellular carcinoma. 3169 37