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Dysregulation of microRNAs in cancer: playing with fire
1Cancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), Barcelona, Catalonia, Spain.
Abstract:
MicroRNAs have emerged as key post-transcriptional regulators of gene expression, involved in various physiological and pathological processes. It was found that several miRNAs are directly involved in human cancers, including lung, breast, brain, liver, colon cancer and leukemia. In addition, some miRNAs may function as oncogenes or tumor suppressors in tumor development. Furthermore, a widespread down-regulation of miRNAs is commonly observed in human cancers and promotes cellular transformation and tumorigenesis. More than 50% of miRNA genes are located in cancer-associated genomic regions or in fragile sites, frequently amplified or deleted in human cancer, suggesting an important role in malignant transformation. A better understanding of the miRNA regulation and misexpression in cancer may ultimately yield further insight into the molecular mechanisms of tumorigenesis and new therapeutic strategies may arise against cancer. Here, we discuss the occurrence of the deregulated expression of miRNAs in human cancers and their importance in the tumorigenic process.
Insights
MicroRNAs (miRNAs) are key gene regulators involved in cancer. Their widespread down-regulation in tumors promotes cancer development, offering potential therapeutic targets.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- MicroRNAs (miRNAs) are crucial post-transcriptional regulators of gene expression.
- Dysregulated miRNA expression is implicated in various human cancers, including lung, breast, brain, liver, colon, and leukemia.
- miRNAs can act as oncogenes or tumor suppressors, influencing tumor development.
Purpose of the Study:
- To discuss the role of deregulated microRNA expression in human cancers.
- To highlight the importance of miRNAs in the tumorigenic process.
- To explore the potential for miRNA-based cancer therapeutics.
Main Methods:
- Review of existing literature on microRNA deregulation in cancer.
- Analysis of miRNA gene locations in cancer-associated genomic regions.
- Discussion of miRNA functions as oncogenes or tumor suppressors.
Main Results:
- A significant down-regulation of miRNAs is commonly observed in human cancers, promoting cellular transformation.
- Over 50% of miRNA genes are located in genomic regions frequently altered in cancer.
- Altered miRNA expression is a hallmark of malignant transformation.
Conclusions:
- Understanding miRNA dysregulation in cancer provides insight into tumorigenesis mechanisms.
- MicroRNAs represent promising targets for novel cancer therapeutic strategies.
- Further research into miRNA biology is essential for advancing cancer treatment.
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