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:C0023890 (
cirrhosis
)
42,195
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Ras association domain family 1 isoform A
(
RASSF1A
) is a tumor suppressor that is methylated in many human cancers, including hepatocellular carcinoma (HCC).
RASSF1A
has been shown to suppress tumors via activation of the Hippo tumor suppressor pathway, including mammalian STE20-like kinase (MST). Amphiregulin (AREG), a target gene for Yes-associated protein (YAP), is a known oncogenic component of the Hippo pathway; however, the tumor-suppressive effect of
RASSF1A
on AREG in regard to regulation of the Hippo pathway remains unclear in HCC. Overexpression of
RASSF1A
in HCC cells, which lack functional
RASSF1A
, significantly inhibited cell proliferation and induced apoptosis by activating the Hippo pathway. Consequently, overexpression of
RASSF1A
inhibited the oncogenic functions of YAP, leading to a significant reduction in AREG secretion via regulation of the Hippo pathway. In human specimens, greater expression of
RASSF1A
was observed in chronic hepatitis/
cirrhosis
than in HCC, whereas expression of YAP and AREG was higher in 81% and 86% of HCC than in corresponding chronic hepatitis/
cirrhosis
, respectively. Furthermore,
RASSF1A
protein gradually decreased as multistep hepatocarcinogenesis progressed from chronic hepatitis/
cirrhosis
dysplastic nodules toward HCC, whereas the protein expression of YAP and AREG gradually increased. These findings provide mechanistic insight into the regulation of YAP and AREG by
RASSF1A
in human multistep hepatocarcinogenesis.
...
PMID:RASSF1A-mediated regulation of AREG via the Hippo pathway in hepatocellular carcinoma. 2359 97