Chronic inflammation increases risk of cancer by as much as 500%

nanoA new study, published by in the journal Cell Stem Cell, has revealed that chronic in the gut increases the of cancer by 500 %.

The increase is linked to microRNA, called miR-34a, which provides cancer the ability to divide asymmetrically.

“A quarter of the world’s population is affected by some type of gut ,” said lead author Xiling Shen, of biomedical engineering at . “These patients always have a much higher chance of developing colon cancer, but it was never clear why. Now we have found a link.”

The scientists used a mouse model to delete microRNA and investigate the effect on the of cancer. The mouse tissue became inflamed without microRNA miR-34A; their grew out of control and formed many tumor-like structures.

Based on the study, Shen’s group concluded that even though miR-34a is active in cancer, it’s actually a good guy. Triggered to act when the gut becomes inflamed, miR-34a forces the process of asymmetrical division, helping to control normal stem cell population

“Typically when you look at tumors and see something that isn’t in normal tissue, you think it’s a bad thing,” said Shen. “But it turns out that, under normal circumstances, these microRNAs are the good guys who only show up when things go wrong. And when you silence them in late-stage cancer, it’s like the super-villain carried off the superhero and the cancer becomes much worse.”

The researchers are investigating potential treatment possibilities and a test which would act as a warning system to catch cancer at an early stage, by detecting elevated levels of miR-34a. A treatment for late-stage cancer would involve the expression of mIR-34 by cancer cells. This would prevent from reverting back to stem calls.


A miR-34a-Numb Feedforward Loop Triggered by Regulates Asymmetric Stem Cell Division in Intestine and Colon Cancer. Pengcheng Bu , Lihua Wang , Kai-Yuan Chen , Tara Srinivasan , Preetish Kadur Lakshminarasimha Murthy , Kuei-Ling Tung , Anastasia Kristine Varanko , Huanhuan Joyce Chen , Yiwei Ai , Sarah King , Steven M. Lipkin , Xiling Shen Cell Stem Cell. DOI10.1016/j.stem.2016.01.006.. Published online 4 February 2016.

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