Related Experiment Video
Updated: Sep 19, 2025

Desthiobiotin-Streptavidin-Affinity Mediated Purification of RNA-Interacting Proteins in Mesothelioma Cells
Published on: April 25, 2018
EZH2: A Crucial Competing Endogenous RNA in Cancer Research-A Scoping Review
Sadra Salehi-Mazandarani1, Sharareh Mahmoudian-Hamedani1, Ziba Farajzadegan2
1Department of Genetics and Molecular Biology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Competing endogenous RNAs (ceRNAs) regulate Enhancer of zeste 2 polycomb repressive complex 2 subunit (EZH2) in cancer. This review identifies 66 ceRNA axes involving EZH2, highlighting their therapeutic potential in cancer treatment.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- Competing endogenous RNAs (ceRNAs) are crucial regulators in cancer progression.
- Enhancer of zeste 2 polycomb repressive complex 2 subunit (EZH2) acts as a ceRNA with a dual role in cancer, presenting a potential therapeutic target.
- Understanding EZH2's ceRNA functions is vital for advancing clinical cancer treatment.
Purpose of the Study:
- To conduct a scoping review of experimentally validated ceRNA axes involving EZH2 in human cancers.
- To identify and categorize the types of RNAs (miRNAs, lncRNAs, mRNAs, circRNAs) participating in these axes.
- To highlight frequently observed ceRNA axes and their components for potential therapeutic targeting.
Main Methods:
- Systematic search of multiple online databases for relevant studies.
- Inclusion of only experimentally validated ceRNA axes involving EZH2.
- Data extraction and categorization of identified RNA molecules and their interactions.
Main Results:
- Identified 66 unique ceRNA axes involving EZH2.
- Cataloged 30 microRNAs (miRNAs), 32 long non-coding RNAs (lncRNAs), 9 messenger RNAs (mRNAs), and 14 circular RNAs (circRNAs).
- Observed recurrent axes like SPRY4-IT1-miR-101-3p-EZH2 and XIST-miR-101-3p-EZH2 across multiple cancer types. Frequent competitors included miR-101-3p, miR-144-3p, miR-124-3p, SPRY4-IT1, XIST, SNHG6, HOXA11-AS, MALAT1, and TUG1.
Conclusions:
- EZH2-containing ceRNA axes are diverse and prevalent in human cancers.
- These axes represent promising targets for novel cancer therapies.
- Further research is necessary to elucidate the precise roles and clinical applicability of these ceRNA networks.
Related Concept Videos
Leaky Scanning
Targeted Cancer Therapies
There are several types of targeted therapies against...
The Nucleolus
Non-LTR Retrotransposons
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
lncRNA - Long Non-coding RNAs

