1 min readNew Data Changes the Way Scientists Explain How Cancer Tumours Develop
Galveston, Texas (Sciasts) — A collaborative research team has uncovered new information that more accurately explains how cancerous tumours grow within the body.
Researchers led by scientists at The University of Texas Medical Branch at Galveston and Baylor College of Medicine found that a losing a section of messenger RNA that was previously thought to transform normal cells into cancerous ones actually acts by blocking a body’s ability suppress the formation of tumours. The finding could completely alter the way that medical science approaches the formation of tumours.
In molecules throughout the body, the three-prime untranslated region, or 3’UTR, is a section of messenger RNA that can alter gene expression. It’s known that shortening this RNA section promotes cancerous tumour growth.
“Researchers have historically thought that this was because 3’UTR shortening induces the expression of proto-oncogenes, normal genes that when altered by mutation or expressed too high, become oncogenes that can transform a normal cell into a cancer cell,” said Eric Wagner, UTMB associate professor in the department of biochemistry and molecular biology. “However, using a combination of computational approaches and cancer cell models, we found that 3’UTR shortening in tumours actually causes tumour-suppressing genes to be turned off.”
In the study, the researchers used “Big data” analyses to reconstruct the RNA thought to form global regulatory networks within breast tumour cells and their matched normal tissues. This approach identified the fact that 3’UTRs are vital in regulating these global regulatory networks. Using this new information, they then disrupted these networks within breast cancer cells to test the effects on tumour growth.
Article adapted from a University of Texas Medical Branch at Galveston news release.
Publication: 3′ UTR shortening represses tumour-suppressor genes in trans by disrupting ceRNA crosstalk. Park, HJ et al. Nature Genetics (May 21, 2018): Click here to view.