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Obesity inhibits key cancer defence mechanism

Posted: 27 April 2018 | | No comments yet

Obesity could enhance cancer development while aspirin might prevent it – a new insight into potential targets for cancer prevention.

Obesity inhibits key cancer defence mechanism

‘Epithelial’ cells lining the surfaces of organs have the intrinsic ability to remove potentially malignant cells from their midst. This is called the ‘epithelial defence against cancer’ mechanism. Normally, the cells sense harmful cells and push them out by the process called cell competition.

To study how obesity affects this defence mechanism, researchers from Hokkaido University and their collaborators bred mice that were designed to express a known cancer-inducing mutant protein called Ras. Epithelial cells usually remove the potentially malignant Ras-transformed cells.

Feeding the Ras mice high-fat diets, which resulted in severe obesity, suppressed the defence mechanism and therefore increased the number of Ras-transformed cells remaining in the tissue. This suppression was seen in the intestine and pancreas, but not in the lungs. Furthermore, a month later the Ras-transformed cells developed a tumour in the pancreas of mice with the high-fat diet. The result supports previous correlations made between intestinal and pancreatic cancer and obesity, but not lung cancer.

Following experiments using the mice model and cultured cells revealed that fatty acids and chronic inflammation cause the suppression of the defence mechanism.

When mice fed a high-fat diet were treated with aspirin, known for its anti-inflammatory properties, the defence mechanism was substantially enhanced. This implies that reinforcing the epithelial defence mechanism with anti-inflammatory drugs could be utilised for cancer prevention.

“This is the first report to show that obesity and chronic inflammation can influence competitive interaction between normal cells and transformed cells. It implies other factors such as infection, smoking, sleeping patterns and aging may also affect cell competition,” says Yasuyuki Fujita of Hokkaido University who led the study.

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