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Updated: Oct 19, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Dysfunction of miR-802 in tumors
Tong Gao1, Mengsha Zou1, Tiancheng Shen1
1Medical Genetics Center, Ningbo University School of Medicine, Ningbo, China.
Abstract:
Recent studies have shown that miR-802 is abnormally expressed in many tumors. miR-802 is expressed at low levels in tissues and cells of gastric cancer, colorectal cancer, breast cancer, cervical cancer, epithelial ovarian cancer, tongue squamous cell carcinoma, oral squamous cell carcinoma, esophageal squamous cell carcinoma, laryngeal squamous cell carcinoma, and melanoma. In contrast, miR-802 is overexpressed in hepatocellular carcinoma, bladder urothelial cancer, osteosarcoma, and cholesteatoma tissue cells. It should be noted that the results of studies on the expression of miR-802 in pancreatic cancer, prostate cancer, and lung cancer are inconsistent. Current studies have found that miR-802 can target and regulate genes in different tumors, and affect the regulation of the Wnt signaling pathway, EMT signaling pathway, PI3K/AKT signaling pathway, ERK signaling pathway, and Hedgehog signaling pathway. At the same time, miR-802 is regulated by the endogenous competition of four ceRNAs, including circDONSON, IGFL2-AS1, MIR155HG, and MIR4435-2HG. This article reviews the abnormal expression of miR-802 in a variety of tumors, expounds the mechanism by which miR-802 affects tumor progression by regulating different target genes, and elaborates the network of miR-802-related ceRNAs. We also summarized the limitations of miR-802 research and looked forward to the potential application of miR-802 in the diagnosis and prognosis of tumors.
Insights
MicroRNA-802 (miR-802) shows altered expression across many cancers, impacting tumor progression by targeting key signaling pathways. Further research into miR-802 could offer new diagnostic and prognostic tools for cancer.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- MicroRNA-802 (miR-802) exhibits dysregulation in various human malignancies.
- Its expression levels vary, being downregulated in cancers like gastric, breast, and colorectal, but upregulated in others such as hepatocellular carcinoma and osteosarcoma.
Purpose of the Study:
- To review the aberrant expression patterns of miR-802 in diverse tumor types.
- To elucidate the molecular mechanisms underlying miR-802's role in tumor progression through target gene regulation and signaling pathway modulation.
- To explore the ceRNA network involving miR-802 and its potential as a diagnostic and prognostic biomarker.
Main Methods:
- Literature review of studies investigating miR-802 expression and function in cancer.
- Analysis of miR-802's regulatory roles in critical cancer signaling pathways (Wnt, EMT, PI3K/AKT, ERK, Hedgehog).
- Examination of the competitive endogenous RNA (ceRNA) network influencing miR-802 levels.
Main Results:
- miR-802 is differentially expressed in numerous cancers, with specific patterns of downregulation or upregulation.
- miR-802 influences tumor progression by targeting various genes and modulating key oncogenic signaling pathways.
- The ceRNA network, involving circDONSON, IGFL2-AS1, MIR155HG, and MIR4435-2HG, plays a role in regulating miR-802.
Conclusions:
- miR-802 is a significant player in tumorigenesis with diverse expression profiles across different cancer types.
- Understanding miR-802's regulatory functions and ceRNA interactions is crucial for developing novel cancer therapies.
- miR-802 holds promise as a potential biomarker for cancer diagnosis and prognosis.
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