LINC‐PINT alleviates lung cancer progression via sponging miR‐543 and inducing PTEN [PDF]
Long intergenic nonprotein coding RNA p53‐induced transcript (LINC‐PINT) has been reported to participate in various cancers. Here, we investigated the effects of LINC‐PINT on lung cancer progression.
Shu Wang +7 more
doaj +5 more sources
Placental Growth Factor Promotes Metastases of Ovarian Cancer Through MiR-543-Regulated MMP7
Background/Aims: Elucidation of the molecular mechanisms underlying ovarian cancer (OC) cell invasion and migration may provide important evidence for developing efficient therapy.
Ning Song +3 more
doaj +4 more sources
Higher miR‐543 levels correlate with lower STK31 expression and longer pancreatic cancer survival [PDF]
AbstractPancreatic cancer (PC) is one of the most malignant gastrointestinal tumors and the 5‐year survival is only 9%. The expression of miRNAs in serum has been proved to be related to tumorigenesis and development of cancers. The miRNA targets and gene targets were predicted in microRNA.org, miRDB, TargetScan, and RNAInter.
Weizhong Yuan, Guangfu Wang
exaly +5 more sources
Upregulation of miR-370 and miR-543 is associated with reduced expression of heat shock protein 40 in spinocerebellar ataxia type 3. [PDF]
Molecular chaperones are important regulators of protein folding and proteasomal removal of misfolded proteins. In spinocerebellar ataxia type 3 (SCA3), the co-chaperone DnaJ homology subfamily B member 1 (DNAJB1 or heat shock protein 40) is recruited to
Bernd O Evert +9 more
doaj +4 more sources
CTGF promotes osteosarcoma angiogenesis by regulating miR-543/angiopoietin 2 signaling
Osteosarcoma is the most common primary solid tumor of bone. It has a high metastatic potential and occurs predominantly in adolescents and young adults. Angiopoietin 2 (Angpt2) is a key regulator in tumor angiogenesis, facilitating tumor growth and metastasis.
Li-Hong Wang +2 more
exaly +4 more sources
MiR-543 Promotes Migration, Invasion and Epithelial-Mesenchymal Transition of Esophageal Cancer Cells by Targeting Phospholipase A2 Group IVA [PDF]
Background/Aims: The aim of this study was to investigate the roles of miR-543 and phospholipase A2 group IVA (PLA2G4A) in cell mobility and the invasiveness cascade in esophageal squamous cell carcinoma (ESCC) and to validate the interactive ...
Huaying Zhao +7 more
doaj +2 more sources
m5C modification of LINC01082 inhibits osteosarcoma progression by modulating the miR-543-TNRC6A axis. [PDF]
Osteosarcoma (OS) is a highly malignant bone tumor primarily affecting children and adolescents, with a significant portion of patients developing metastasis, leading to poor prognosis. Recent studies have identified long noncoding RNAs (lncRNAs) as critical regulators in cancer progression.
Hu Y +8 more
europepmc +4 more sources
miR‑543 acts as a novel oncogene in oral squamous cell carcinoma by targeting CYP3A5. [PDF]
MicroRNAs (miRNAs/miRs) are small non‑coding RNAs that can act as oncogenes or tumor‑suppressor genes in human cancer. Previous studies have revealed that abnormal expression of miRNAs is closely associated with tumor cell cycle, differentiation, growth and apoptosis.
Wang L +7 more
europepmc +4 more sources
miR-543 Inhibits the Occurrence and Development of Intrauterine Adhesion by Inhibiting the Proliferation, Migration, and Invasion of Endometrial Cells. [PDF]
Objective. To explore the function of miR‐543 in endometrial cells and the possible mechanism of regulating the occurrence and development of intrauterine adhesion. Method. Endometrial epithelial cells and endometrial adenocarcinoma cells were transfected with miR‐543 mimics and miR‐543 inhibitor as the experimental group and were tested with the ...
Liu X, Xu Q, Chen C, Duan H.
europepmc +4 more sources
miR-543 functions as a tumor suppressor in glioma in vitro and in vivo. [PDF]
Gliomas are the most common primary central nervous system tumors and account for approximately 80% of malignant brain tumors. MicroRNAs (miRNAs) are a class of small non-coding, regulatory RNA molecules that mediate the expression levels of specific proteins.
Xu L +5 more
europepmc +4 more sources

