e., physical inactivity, obesity, diabetes treatment types and high-saturated-fat diet), which are also independent risk factors for cancer. Furthermore, insulin-resistant diabetic cancer patients are characterized by a worst

outcome compared to non-diabetic cancer patients and this depends on an increased cancer-site specific mortality, which reaches statistical significance for breast, endometrial and colorectal cancers, and a reduced sensitivity to anticancer therapies (1). It has been suggested that the major mechanism responsible for the increased cancer risk Inhibitors,research,lifescience,medical in diabetics and the poor prognosis of patients with malignancies associated to insulin-resistance is the resulting hyperinsulinemia. Chronic hyperinsulinemia, indeed, favors cancer initiation and/or progression due to the direct mitogenic activity of Selleckchem BIIB057 insulin on epithelial cells and its ability to stimulate cells indirectly Inhibitors,research,lifescience,medical by increasing the levels of other modulators of proliferation, such as insulin-like

growth factor (IGF-1) and sex hormones. In addition, cancer cells are characterized by increased expression of insulin and IGF-1 receptors and by the inability to down-regulate these receptors in response to hyperinsulinemia. Inhibitors,research,lifescience,medical Thus, the increased levels of insulin and IGF-1 in diabetic cancer patients lead to abnormal activation of insulin and IGF-1 receptor signaling in tumors cells, potentially explaining the influence of hyperinsulinemia on tumor prognosis and poor response to anticancer therapies. In fact, insulin and IGF-1 are responsible for a strong activation of PI3K/AKT and MAPK pathways and this results in a cascade of proliferative and anti-apoptotic events favoring tumor Inhibitors,research,lifescience,medical progression, Inhibitors,research,lifescience,medical drug resistance and poor patient’s outcome (2). Noteworthy, the same mechanism of insulin resistance and subsequent hyperinsulinemia is likely responsible for the increased cancer risk and the poor prognosis of malignancies associated to other conditions such as obesity and metabolic syndrome (3). In this issue, Chen et al. present a study which

addresses the role of insulin and activation of AKT pathway on oxaliplatin antiproliferative activity in human colorectal cancer cells (4). The authors suggest that high insulin levels in the Phosphoprotein phosphatase extracellular environment are responsible for a significant inhibition of oxaliplatin cytotoxic activity, which could be mediated by the activation of the PI3K/AKT pathway. Of note, the selective pharmacological inhibition of PI3K results in the re-establishment of oxaliplatin-induced cytotoxicity. This study highlights two major issues which may be relevant for future clinical management of obesity-associated colorectal cancers: the role played by hyperinsulinemia and activation of PI3K/AKT pathway in favoring drug resistance.