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Researchers identify long non-coding RNA which modulates colorectal cancer metabolism.

Long non-coding RNAs (lncRNA) are unusual in that they don’t encode proteins like normal RNA. Yet they do play a role in regulating cellular functions and interest cancer researchers.  Now, researchers at The MD Anderson Cancer Center have found that a specific lncRNA called CCAT2 regulates cancer metabolism both in vivo and in vitro. The data was presented at the 2015 American Association for Cancer Research (AACR) Annual Meeting.

The team explain that altered energy metabolism is a cancer hallmark as malignant cells tailor their metabolic pathways to meet their energy requirements.  The current study found that CCAT2 regulated cancer metabolism in an allele-specific manner that appears to match a known risk associated with colon cancer. This result was novel in that it uncovered complex mechanisms of cancer metabolism and regulation controlled by a long non-coding RNA.

Alleles are gene forms that cause genetic traits, and can be specific for disease development, state the researchers; adding that, some alleles are associated with a higher risk for cancer. To better understand how lncRNAs play a role in cancer metabolism the team looked at glutamine, one of the major nutrients that fuel cellular metabolism.  The pathways that use these nutrients are often changed by cancer.

The current study observed that the long non-coding RNA CCAT2 resulted in a newly formed RNA protein complex that regulated the metabolic enzyme glutaminase 1 (GLS1).  The lncRNA, located near a DNA sequence called SNP known to be associated with an increased risk of colon cancer, accomplishes this by binding to a protein complex called CFIm that regulates genetic splicing of GLS1, state the team. This binding displays similarities to known genetic risks tied to SNP, indicating that this stronger interaction may be associated with the higher-risk allele.

The team state that while there may not be an increased risk for cancer results from this interaction, it may contribute to it, adding that more studies are needed to learn more about this new development.

Source:  The University of Texas MD Anderson Cancer Center 

Michelle Petersen View All

I am an award-winning science journalist and health industry veteran who has taught and worked in the field.

Featured by numerous prestigious brands and publishers, I specialize in clinical trial innovation–-expertise I gained while working in multiple positions within the private sector, the NHS, and Oxford University, where I taught undergraduates the spectrum of biological sciences integrating physics for over four years.

I recently secured tenure as a committee member for the Smart Works Charity, which helps women find employment in the UK.

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