Obesity, the PI3K/Akt signal pathway and colon cancer

Authors


Professor X-F Huang and Dr J-Z Chen, School of Health Sciences, The University of Wollongong, Northfield Avenue, Wollongong, NSW2522, Australia. E-mail: xhuang@uow.edu.au; jiezhong@uow.edu.au

Summary

Obesity is currently reaching epidemic levels worldwide and is a major predisposing factor for a variety of life-threatening diseases including diabetes, hypertension and cardiovascular diseases. Recently, it has also been suggested to be linked with cancer.

Epidemiological studies have shown that obesity increases the risk of colon cancer by 1.5–2 fold with obesity-associated colon cancer accounting for 14–35% of total incidence. Several factors, altered in obesity, may be important in cancer development including increased levels of blood insulin, insulin-like growth factor I, leptin, TNF-α, IL-6 as well as decreased adiponectin. A unifying characteristic of all these factors is that they increase the activity of the PI3K/Akt signal pathway. The PI3K/Akt signal pathway in turn activates signals for cell survival, cell growth and cell cycle leading to carcinogenesis. Here we review the evidence that PI3K/Akt and its downstream targets are important in obesity-associated colon cancer and thus, that targeted inhibition of this pathway could be employed for the prevention of obesity-associated colon cancer and incorporated into the therapy regime for those with irremovable colon cancers.

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