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BIOMARKER:

miR-199a overexpression

i
Other names: MIR199A, MicroRNA 199a, MIR 199A, MIR-199A
7ms
MiR-199a-5p Decreases Esophageal Cancer Cell Proliferation Partially through Repression of Jun-B. (PubMed, Cancers (Basel))
Either forced expression of miR-199a-5p or Jun-B silencing led to a significant decrease in cellular proliferation as well as in AP-1 promoter activity. Our results provide evidence that miR-199a-5p functions as a tumor suppressor in esophageal cancer cells by regulating cellular proliferation, partially through repression of Jun B.
Journal
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MIR199A (MicroRNA 199a) • JUN (Jun proto-oncogene)
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miR-199a overexpression
7ms
miR-199a/214 cluster enhances prostate cancer sensitiveness to nimotuzumab via targeting TBL1XR1. (PubMed, Kaohsiung J Med Sci)
In summary, our data indicated that miR-199a/214 cluster play a crucial role in enhancing the inhibitory effect of nimotuzumab on PCa development by downregulating TBL1XR1 and modulating Wnt/β-catenin and EGFR signaling pathways. These findings offer a novel therapeutic approach for the treatment of prostate cancer.
Journal
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MIR199A (MicroRNA 199a) • MIR214 (MicroRNA 214) • TBL1XR1 (TBL1X Receptor 1)
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miR-199a overexpression
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TheraCIM (nimotuzumab)
8ms
LncRNA SNHG1 upregulates FANCD2 and G6PD to suppress ferroptosis by sponging miR-199a-5p/3p in hepatocellular carcinoma. (PubMed, Drug Discov Ther)
In addition, knockdown of SNHG1 increased erastin-mediated ferroptosis, iron accumulation, and lipid peroxidation...Moreover, a signature based on expression of SNHG1, FANCD2, and G6PD was identified as being associated with overall survival and the immunological microenvironment in HCC. Collectively, this study identified the SNHG1-miR-199a-FANCD2/G6PD axis in HCC, which is a potential marker for the prognosis and therapy of this tumor.
Journal
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MIR199A1 (MicroRNA 199a-1) • FANCD2 (FA Complementation Group D2) • G6PD (Glucose-6-Phosphate Dehydrogenase) • MIR199A (MicroRNA 199a) • SNHG1 (Small Nucleolar RNA Host Gene 1)
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miR-199a overexpression
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erastin
over1year
MiR-199a-3p Induces Mesenchymal to Epithelial Transition of Keratinocytes by Targeting RAP2B. (PubMed, Int J Mol Sci)
These findings suggest that miR-199a-3p inhibits the EMT process by targeting RAP2B. Inhibitors of RAP2B or FAK may be effective therapeutic agents for CSCC.
Journal
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MIR199A1 (MicroRNA 199a-1) • MIR199A (MicroRNA 199a)
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miR-199a overexpression
almost2years
miR-199a-3p/5p regulate tumorgenesis via targeting Rheb in non-small cell lung cancer. (PubMed, Int J Biol Sci)
In addition, miR-199a-3p/5p has been shown to enhance the sensitivity of gefitinib to EGFR-T790M in NSCLC. Collectively, these results prove that miR-199a-3p/5p can act as cancer suppressor genes to inhibit the mTOR signaling pathway by targeting Rheb, which in turn inhibits the regulatory process of NSCLC. Thus, to investigate the anti-cancer effect of pre-miR-199a/Rheb/mTOR axis in NSCLC, miR-199a-3p and miR-199a-5p have the potential to become an early diagnostic marker or therapeutic target for NSCLC.
Journal
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EGFR (Epidermal growth factor receptor) • MIR199A1 (MicroRNA 199a-1) • MIR199A (MicroRNA 199a) • RHEB (Ras Homolog, MTORC1 Binding)
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EGFR T790M • miR-199a overexpression
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gefitinib
almost2years
Exosomal MiR-199a-5p Inhibits Tumorigenesis and Angiogenesis by Targeting VEGFA in Osteosarcoma. (PubMed, Front Oncol)
Our results demonstrated that miR-199a-5p could be transported from osteosarcoma cells to HUVECs through exosomes, subsequently targeting VEGFA and inhibiting the growth and angiogenesis of osteosarcoma. Therefore, miR-199a-5p may act as a biomarker in the diagnosis and treatment of osteosarcoma.
Journal
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TP53 (Tumor protein P53) • MIR199A (MicroRNA 199a) • MIR223 (MicroRNA 223)
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miR-199a overexpression