MiR-93 suppresses cell proliferation and invasion by targeting ZNF322 in human hepatocellular carcinoma
نویسندگان
چکیده
Introduction This study aimed to investigate the biological role of microRNA 93 (miR-93), a novel tumor-related miRNA, in human hepatocellular carcinoma (HCC) and elucidate potential molecular mechanisms involved. Material methods Quantitative real-time polymerase chain reaction (qRT-PCR) was conducted determine expression miR-93 HCC tissues cell lines. The log-rank test Kaplan-Meier survival analysis were performed evaluate relationship between overall survival. MTT assay, colony formation Transwell migration invasion assays carried out exam proliferation, formation, invasion, respectively. Murine xenograft models established effect on tumor growth vivo. TargetScan online software applied predict target miR-93. Luciferase reporter used validate direct binding its putative target. Results Here we found that significantly down-regulated Patients with decreased had shorter Functional investigations demonstrated over-expression suppressed weakened clonogenic ability, slowed down invasion; whereas depletion facilitated invasion. MiR-93 retarded assay rescue revealed zinc finger protein 322 (ZNF322) mediated inhibitory effects proliferation motility. Conclusions Our data may provide some evidence for miR-93/ZNF322 axis candidate therapeutic HCC.
منابع مشابه
miR-92a promotes hepatocellular carcinoma cells proliferation and invasion by FOXA2 targeting
Objective(s): MicroRNAs (miRNAs) are considered as powerful, post-transcriptional regulators of gene expression in hepatocellular carcinoma cells (HCC). However, the function of miR-92a is still unclear in HCC. Materials and Methods: Expression of miR-92a in human HCC cell lines was evaluated using qRT-PCR. MTT assay and transwell assay were used to examine the function of miR-92a in HepG2 and ...
متن کاملMiR-144 suppresses cell proliferation, migration, and invasion in hepatocellular carcinoma by targeting SMAD4
BACKGROUND/AIM Increasing evidence show microRNAs (miRNAs) are engaged in hepatocellular carcinoma (HCC). The aim of this study was to investigate the role of miR-144 in HCC, as well as to identify its underlying mechanism. METHODS The expression levels of miR-144 were assessed in multiple HCC cell lines, as well as in liver tissues from patients with HCC. We further examined the effects of m...
متن کاملMiR-502-3P suppresses cell proliferation, migration, and invasion in hepatocellular carcinoma by targeting SET
BACKGROUND/AIM Increasing evidences show that microRNAs are engaged in hepatocellular carcinoma (HCC). The aim of this study was to investigate the role of miR-502-3P in HCC and to identify its underlying mechanism. METHODS The expression levels of miR-502-3P were assessed in multiple HCC cell lines and in liver tissues of patients with HCC. We further examined the effects of miR-502-3P on ma...
متن کاملMiR-493 suppresses the proliferation and invasion of gastric cancer cells by targeting RhoC
Objective(s):MiRNAs have been proposed to be key regulators of tumorigenesis, progression and metastasis. However, their effect and prognostic value in gastric cancer is still poorly known. Materials and Methods: Gastric cancer cell lines were cultured. Tissue samples obtained from 36 gastric cancer patients were used for quantitative real-time PCR (qRT-PCR) analysis. The tissue microarrays (T...
متن کاملmiR-506 inhibits cell proliferation and invasion by targeting TET family in colorectal cancer
Objective(s): Ten-eleven translocation (TET) family members have been shown to be involved in the development of many tumors. However, the biological role of the TET family and its mechanism of action in colorectal carcinogenesis and progression remain poorly understood. Materials and Methods:We measured the expression levels of TET family members in colorectal cancer (CRC) specimens, in the c...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Archives of Medical Science
سال: 2021
ISSN: ['2657-7941']
DOI: https://doi.org/10.5114/aoms/105350