Related Experiment Video
Updated: Mar 29, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
Dysregulation of microRNA biogenesis machinery in cancer
1a Cardiovascular Research Institute, University of California , San Francisco , CA , USA.
Abstract:
MicroRNAs (miRNAs) are integral to the gene regulatory network. A single miRNA is capable of controlling the expression of hundreds of protein coding genes and modulate a wide spectrum of biological functions, such as proliferation, differentiation, stress responses, DNA repair, cell adhesion, motility, inflammation, cell survival, senescence and apoptosis, all of which are fundamental to tumorigenesis. Overexpression, genetic amplification, and gain-of-function mutation of oncogenic miRNAs ("onco-miRs") as well as genetic deletion and loss-of-function mutation of tumor suppressor miRNAs ("suppressor-miRs") are linked to human cancer. In addition to the dysregulation of a specific onco-miR or suppressor-miRs, changes in global miRNA levels resulting from a defective miRNA biogenesis pathway play a role in tumorigenesis. The function of individual onco-miRs and suppressor-miRs and their target genes in cancer has been described in many different articles elsewhere. In this review, we primarily focus on the recent development regarding the dysregulation of the miRNA biogenesis pathway and its contribution to cancer.
Insights
MicroRNAs (miRNAs) regulate gene expression and cell functions. This review focuses on how defects in miRNA biogenesis contribute to cancer development.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression, influencing critical cellular processes like proliferation, apoptosis, and inflammation.
- Dysregulation of specific miRNAs, termed onco-microRNAs (onco-miRs) and tumor suppressor microRNAs (suppressor-miRs), is implicated in human cancers.
- Aberrant miRNA levels can arise from defects in the miRNA biogenesis pathway, contributing to tumorigenesis.
Purpose of the Study:
- To review recent advancements in understanding the dysregulation of the miRNA biogenesis pathway.
- To explore the contribution of altered miRNA biogenesis to cancer development.
- To highlight the role of global miRNA level changes in tumorigenesis.
Main Methods:
- Literature review of recent research on miRNA biogenesis and cancer.
- Analysis of studies focusing on the impact of miRNA biogenesis defects on tumorigenesis.
- Synthesis of information on the role of onco-miRs and suppressor-miRs in cancer.
Main Results:
- Defects in miRNA biogenesis pathways lead to altered global miRNA levels, contributing to cancer.
- Specific onco-miRs and suppressor-miRs, along with their target genes, are crucial in cancer development.
- The review consolidates current knowledge on the link between miRNA biogenesis and cancer.
Conclusions:
- Dysregulation of miRNA biogenesis is a significant factor in human cancer.
- Understanding these pathways offers potential therapeutic targets for cancer treatment.
- Further research into miRNA biogenesis defects is essential for cancer research.
Related Concept Videos
MicroRNAs
MicroRNAs
MicroRNAs
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
mTOR Signaling and Cancer Progression
Abnormal Proliferation

