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Updated: Apr 10, 2026

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Published on: April 6, 2012
MicroRNA-802 suppresses breast cancer proliferation through downregulation of FoxM1
1Department of Breast Cancer, Hubei Cancer Hospital, Wuhan, Hubei 430079, P.R. China.
Abstract:
An increasing number of studies have shown that microRNAs (miRNAs) are critical in tumor cell proliferation, as they modulate key gene transcripts. In the present study, the expression and roles of miRNA (miR)‑802 were analyzed by quantitative polymerase chain reaction in breast cancer cells. The results showed that expression levels of miR‑802 were significantly reduced in breast cancer tissues and cells compared with those of normal tissue and normal breast epithelial cells. In vitro and in vivo experiments demonstrated that miR‑802 overexpression inhibited cell proliferation in MCF‑7 breast cancer cells and tumor growth in nude mice, respectively. Furthermore, mechanistic investigation with western blotting and luciferase reporter assays revealed that miR‑802 overexpression downregulated protein expression levels of Forkhead box protein M1 (FoxM1). Therefore, the results of the present study provided evidence for a previously undetermined miR‑802/FoxM1 molecular network, which was involved in the regulation of breast cancer cell proliferation.
Insights
MicroRNA-802 (miR-802) is reduced in breast cancer, inhibiting tumor cell proliferation and growth. Overexpression of miR-802 downregulates Forkhead box protein M1 (FoxM1), revealing a novel regulatory network.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) play crucial roles in regulating gene expression, impacting processes like tumor cell proliferation.
- Dysregulation of specific miRNAs is frequently observed in various cancers, including breast cancer.
Purpose of the Study:
- To investigate the expression and functional role of microRNA (miR)-802 in breast cancer.
- To elucidate the molecular mechanisms underlying miR-802's function in breast cancer cell proliferation.
Main Methods:
- Quantitative polymerase chain reaction (qPCR) was used to assess miR-802 expression levels in breast cancer tissues and cells.
- In vitro assays (MCF-7 cells) and in vivo experiments (nude mice) were conducted to evaluate the effects of miR-802 overexpression on cell proliferation and tumor growth.
- Western blotting and luciferase reporter assays were employed to identify downstream targets of miR-802.
Main Results:
- miR-802 expression was significantly downregulated in breast cancer tissues and cells compared to normal controls.
- Overexpression of miR-802 inhibited proliferation of MCF-7 breast cancer cells and suppressed tumor growth in vivo.
- Mechanistic studies revealed that miR-802 directly downregulates the protein expression of Forkhead box protein M1 (FoxM1).
Conclusions:
- The study identifies a novel molecular network involving miR-802 and FoxM1 in the regulation of breast cancer cell proliferation.
- miR-802 acts as a tumor suppressor in breast cancer by inhibiting cell proliferation and tumor growth, partly through the downregulation of FoxM1.
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