4.3 Review

2017 update on the relationship between diabetes and colorectal cancer: epidemiology, potential molecular mechanisms and therapeutic implications

Journal

ONCOTARGET
Volume 8, Issue 11, Pages 18456-18485

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.14472

Keywords

hyperglycemia; inflammation; diabetic kidney disease; colon cancer; diabetes mellitus

Funding

  1. FIS/FEDER [PI14/01650, PI13/00047, PI14/00386, PIE13/00051, PI13/01873, PI13/00802, PI14/00883, PI15/00298, PI15/01460, PI16/02057, PI16/01900, CP09/00229, CP14/00133, CPII15/00027, SAF2012-38830, CP12/03262 ISCIII-RETIC REDinREN RD12/0021 RD16/0009, RETICEF RD12/0043/0008]
  2. CIBER in Diabetes and Associated Metabolic Disorders (CIBERDEM, ISCIII)
  3. Biobanco IIS-FJD [PT13/0010/0012, FP7-HEALTH-2013-INNOVATION-1-602422]
  4. Comunidad de Madrid [S2010/BMD-2378]
  5. CYTED IBERERC
  6. CYTED IBERERC, Programa Intensificacion Actividad Investigadora (ISCIII)
  7. Sociedad Espanola de Nefrologia y Fundacion Renal Inigo Alvarez de Toledo
  8. Programa Miguel Servet
  9. Programa Joan Rodes

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Worldwide deaths from diabetes mellitus (DM) and colorectal cancer increased by 90% and 57%, respectively, over the past 20 years. The risk of colorectal cancer was estimated to be 27% higher in patients with type 2 DM than in non-diabetic controls. However, there are potential confounders, information from lower income countries is scarce, across the globe there is no correlation between DM prevalence and colorectal cancer incidence and the association has evolved over time, suggesting the impact of additional environmental factors. The clinical relevance of these associations depends on understanding the mechanism involved. Although evidence is limited, insulin use has been associated with increased and metformin with decreased incidence of colorectal cancer. In addition, colorectal cancer shares some cellular and molecular pathways with diabetes target organ damage, exemplified by diabetic kidney disease. These include epithelial cell injury, activation of inflammation and Wnt/beta-catenin pathways and iron homeostasis defects, among others. Indeed, some drugs have undergone clinical trials for both cancer and diabetic kidney disease. Genome-wide association studies have identified diabetes-associated genes (e.g. TCF7L2) that may also contribute to colorectal cancer. We review the epidemiological evidence, potential pathophysiological mechanisms and therapeutic implications of the association between DM and colorectal cancer. Further studies should clarify the worldwide association between DM and colorectal cancer, strengthen the biological plausibility of a cause-and-effect relationship through characterization of the molecular pathways involved, search for specific molecular signatures of colorectal cancer under diabetic conditions, and eventually explore DM-specific strategies to prevent or treat colorectal cancer.

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