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Functions and mechanisms of microRNA-31 in human cancers
1Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Abstract:
MicroRNAs can exhibit opposite functions in different tumors. MiR-31 is a representative example as it can not only enhance tumor development and progression in pancreatic cancer, colorectal cancer and so on, but also inhibit tumorigenesis and induce apoptosis in ovarian cancer, prostate cancer and etc. The mechanism underlying its' pleiotropy remains unknown. Several recent studies that focused on the global gene expression changes caused by aberrant miR-31 provided information on the upstream and downstream events associated with deregulated miR-31. MiR-31 might interact with a number of signaling pathways including RAS/MARK, PI3K/AKT and RB/E2F to play its opposite functions. This review summarizes the target genes and pathways associated with miR-31 and examines the mechanisms underlying the function of miR-31. The resulting hypothesis is possible that the tissue-specific features of adenocarcinoma and squamous cell cancer and the positive feedback loop consists of miR-31 and its upstream and downstream may account for the diversity of miR-31 functions.
Insights
MicroRNAs like miR-31 have dual roles in cancer, promoting some tumors while inhibiting others. This review explores the molecular mechanisms behind miR-31
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression.
- Aberrant miRNA expression is implicated in various human diseases, including cancer.
- MiR-31 is known to play contrasting roles in different cancer types, acting as an oncogene or tumor suppressor.
Purpose of the Study:
- To review the known target genes and signaling pathways influenced by miR-31.
- To elucidate the mechanisms responsible for miR-31's pleiotropic functions in cancer.
- To propose a hypothesis explaining the opposing roles of miR-31 in different tumor types.
Main Methods:
- Literature review of studies investigating global gene expression changes induced by miR-31.
- Analysis of signaling pathways potentially modulated by miR-31, including RAS/MARK, PI3K/AKT, and RB/E2F.
- Synthesis of findings to formulate a hypothesis on miR-31's functional diversity.
Main Results:
- MiR-31 targets numerous genes and interacts with key cancer-related signaling pathways.
- Evidence suggests miR-31 can promote tumor development (e.g., pancreatic, colorectal cancer) or inhibit it (e.g., ovarian, prostate cancer).
- Specific pathways like RAS/MARK, PI3K/AKT, and RB/E2F are implicated in mediating miR-31's opposing functions.
Conclusions:
- The pleiotropy of miR-31 is likely influenced by tissue-specific characteristics of adenocarcinoma and squamous cell carcinoma.
- A positive feedback loop involving miR-31 and its regulatory network may contribute to its diverse functional outcomes.
- Understanding miR-31's complex roles is crucial for developing targeted cancer therapies.
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