MiR-30e-3p Influences Tumor Phenotype through
Animals
Antineoplastic Agents
/ pharmacology
Binding Sites
Carcinogens
Carcinoma, Hepatocellular
/ drug therapy
Cell Proliferation
Cohort Studies
Diethylnitrosamine
Disease Models, Animal
Down-Regulation
Drug Resistance, Neoplasm
Epithelial Cell Adhesion Molecule
/ metabolism
Gene Silencing
Genes, Tumor Suppressor
Genes, p53
/ genetics
Hep G2 Cells
Heterografts
Humans
Liver Neoplasms
/ drug therapy
MicroRNAs
/ metabolism
Mutation
Neoplasm Invasiveness
Neoplasm Proteins
/ genetics
Neoplastic Stem Cells
PTEN Phosphohydrolase
/ metabolism
Phenotype
Proliferating Cell Nuclear Antigen
/ metabolism
Proto-Oncogene Proteins c-mdm2
/ genetics
Rats
Sorafenib
/ pharmacology
Tissue Array Analysis
Tumor Suppressor Protein p53
/ genetics
Journal
Cancer research
ISSN: 1538-7445
Titre abrégé: Cancer Res
Pays: United States
ID NLM: 2984705R
Informations de publication
Date de publication:
15 04 2020
15 04 2020
Historique:
received:
06
02
2019
revised:
29
06
2019
accepted:
28
01
2020
pubmed:
6
2
2020
medline:
21
10
2020
entrez:
5
2
2020
Statut:
ppublish
Résumé
The molecular background of hepatocellular carcinoma (HCC) is highly heterogeneous, and biomarkers predicting response to treatments are an unmet clinical need. We investigated miR-30e-3p contribution to HCC phenotype and response to sorafenib, as well as the mutual modulation of
Identifiants
pubmed: 32015093
pii: 0008-5472.CAN-19-0472
doi: 10.1158/0008-5472.CAN-19-0472
doi:
Substances chimiques
Antineoplastic Agents
0
Carcinogens
0
EPCAM protein, human
0
Epithelial Cell Adhesion Molecule
0
MIRN30b microRNA, human
0
MicroRNAs
0
Neoplasm Proteins
0
Proliferating Cell Nuclear Antigen
0
TP53 protein, human
0
Tumor Suppressor Protein p53
0
p27 antigen
0
Diethylnitrosamine
3IQ78TTX1A
Sorafenib
9ZOQ3TZI87
MDM2 protein, human
EC 2.3.2.27
Proto-Oncogene Proteins c-mdm2
EC 2.3.2.27
PTEN Phosphohydrolase
EC 3.1.3.67
PTEN protein, human
EC 3.1.3.67
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1720-1734Informations de copyright
©2020 American Association for Cancer Research.