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Published on: April 25, 2022
Aberrant regulation and function of microRNAs in cancer
Brian D Adams1, Andrea L Kasinski2, Frank J Slack1
1Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06520, USA.
Abstract:
Malignant neoplasms are consistently among the top four leading causes of death in all age groups in the United States, despite a concerted effort toward developing novel therapeutic approaches. Our understanding of and therapeutic strategy for treating each of these neoplastic diseases have been improved through decades of research on the genetics, signaling pathways, and cellular biology that govern tumor cell initiation, progression and maintenance. Much of this work has concentrated on post-translational modifications and abnormalities at the DNA level, including point mutations, amplifications/deletions, and chromosomal translocations, and how these aberrant events affect the expression and function of protein-coding genes. Only recently has a novel class of conserved gene regulatory molecules been identified as a major contributor to malignant neoplastic disease. This review focuses on how these small non-coding RNA molecules, termed microRNAs (miRNAs), can function as oncogenes or tumor suppressors, and how the misexpression of miRNAs and dysregulation of factors that regulate miRNAs contribute to the tumorigenic process. Specific focus is given to more recently discovered regulatory mechanisms that go awry in cancer, and how these changes alter miRNA expression, processing, and function.
Insights
MicroRNAs (miRNAs) are small non-coding RNAs that can act as oncogenes or tumor suppressors. Their misexpression and dysregulation are increasingly recognized as key contributors to cancer development and progression.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Malignant neoplasms remain a leading cause of death in the US, driving research into novel therapeutic strategies.
- Decades of research have focused on genetic and cellular mechanisms of cancer, including DNA-level abnormalities and post-translational modifications.
- Recent discoveries highlight small non-coding RNA molecules, microRNAs (miRNAs), as significant contributors to neoplastic diseases.
Purpose of the Study:
- To review the role of microRNAs (miRNAs) in cancer, focusing on their function as oncogenes or tumor suppressors.
- To explore how miRNA misexpression and dysregulation contribute to tumorigenesis.
- To examine recently identified regulatory mechanisms affecting miRNA expression, processing, and function in cancer.
Main Methods:
- Review of current scientific literature on microRNA biology and cancer.
- Analysis of genetic and molecular mechanisms underlying miRNA regulation in neoplastic diseases.
- Focus on aberrant regulatory pathways impacting miRNA expression and function.
Main Results:
- MicroRNAs (miRNAs) can function as either oncogenes or tumor suppressors.
- Misexpression and dysregulation of miRNAs are implicated in the development and progression of various cancers.
- Altered regulatory mechanisms significantly impact miRNA expression, processing, and function in the tumorigenic process.
Conclusions:
- MicroRNAs (miRNAs) represent a critical class of gene regulatory molecules in cancer.
- Understanding miRNA dysregulation offers potential for novel cancer therapeutic strategies.
- Further research into miRNA regulatory networks is essential for advancing cancer treatment.
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