Related Experiment Video
Updated: Jun 25, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
Let-7 and miR-200 microRNAs: guardians against pluripotency and cancer progression
1The Ben May Department for Cancer Research, The University of Chicago, Chicago, Illinois 60637, USA. mpeter@uchicago.edu
Abstract:
Micro (mi)RNAs are emerging as important regulators of cellular differentiation, their importance underscored by the fact that they are often dysregulated during carcinogenesis. Two evolutionary conserved families, let-7 and miR-200, regulate key differentiation processes during development. Loss of let-7 in cancer results in reverse embryogenesis and dedifferentiation, and miR-200 has been identified as a powerful regulator of epithelial-to-mesenchymal transition (EMT). Recent findings have connected let-7 with stem cell maintenance and point at a connection between EMT and stem cell formation. A part of tumor progression can be viewed as a continuum of progressive dedifferentiation (EMT) with a cell at the endpoint that has stem cell-like properties. I propose that steps of this process are driven by specific changes in the expression of let-7 and miR-200 family members.
Insights
MicroRNAs (miRNAs) regulate cell differentiation and are crucial in cancer. The let-7 and miR-200 families are key players in development, with their dysregulation linked to tumor progression and stem cell properties.
Area of Science:
- Molecular Biology
- Developmental Biology
- Cancer Research
Background:
- MicroRNAs (miRNAs) are critical regulators of cellular differentiation.
- Dysregulation of miRNAs is frequently observed in carcinogenesis.
- The let-7 and miR-200 miRNA families are evolutionarily conserved and play vital roles in development.
Purpose of the Study:
- To explore the role of let-7 and miR-200 in cellular differentiation and cancer.
- To investigate the connection between epithelial-to-mesenchymal transition (EMT), stem cell properties, and miRNA expression.
- To propose a model where changes in let-7 and miR-200 drive tumor progression.
Main Methods:
- Literature review and synthesis of existing research on let-7, miR-200, EMT, and stem cell biology.
- Analysis of the proposed continuum of dedifferentiation during tumor progression.
- Hypothesizing the role of specific miRNA family expression changes.
Main Results:
- Loss of let-7 is associated with reverse embryogenesis and dedifferentiation in cancer.
- miR-200 is a key regulator of epithelial-to-mesenchymal transition (EMT).
- let-7 is linked to stem cell maintenance, suggesting a connection between EMT and stem cell formation.
Conclusions:
- Tumor progression can be conceptualized as a continuum of dedifferentiation (EMT) leading to stem cell-like properties.
- Specific alterations in let-7 and miR-200 family expression are proposed to drive key steps in this process.
- Understanding these miRNA dynamics offers insights into cancer development and potential therapeutic targets.
Related Concept Videos
MicroRNAs
MicroRNAs
MicroRNAs
Induced Pluripotent Stem Cells
Somatic cells are...
Induced Pluripotent Stem Cells
Induced Pluripotent Stem Cells

