Possible involvement of hyperlipidemia in increasing risk of colorectal tumor development in human familial adenomatous polyposis

Jpn J Clin Oncol. 2006 Mar;36(3):166-71. doi: 10.1093/jjco/hyi233. Epub 2006 Feb 14.

Abstract

Background: Familial adenomatous polyposis (FAP) results from germline adenomatous polyposis coli (APC) gene mutations and many affected patients die from colorectal cancers which arise from colorectal polyps. We previously reported that two strains of Apc gene-deficient mice developing multiple intestinal polyps exhibit a hyperlipidemic state. The triglyceride (TG) levels were approximately 10-fold higher than the levels observed in wild-type mice.

Methods: To examine whether a positive relationship might exist between hyperlipidemia and colorectal tumor development in FAP patients, as with Apc gene-deficient mice, a pilot experiment was performed using readily available clinical data such as ages, serum lipid levels, number of colorectal polyps and cancer development in 28 FAP patients from the National Cancer Center Hospital, Japan.

Results: The overall prevalence of hyperlipidemia in FAP cases was 58%. Average TG levels in the 40-60 year age groups of FAP patients were > or =150 mg/dl (the defined threshold level of hyperlipidemia). Moreover, there was a tendency for higher serum TG levels in patients who developed colorectal cancer, as compared with those without colorectal cancer.

Conclusions: These results show that a hyperlipidemic state occurs in FAP patients. Although it is weaker than that in Apc gene-deficient mice, it may be linked to colon tumor development. These data warrant further studies for wider populations of FAP patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenomatous Polyposis Coli / complications*
  • Adenomatous Polyposis Coli / genetics
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Colorectal Neoplasms / epidemiology
  • Colorectal Neoplasms / etiology
  • Female
  • Genes, APC*
  • Germ-Line Mutation*
  • Humans
  • Hyperlipidemias / epidemiology*
  • Intestinal Polyps / epidemiology*
  • Intestinal Polyps / etiology
  • Male
  • Mice
  • Middle Aged
  • Pilot Projects
  • Prevalence
  • Rectal Neoplasms / epidemiology
  • Rectal Neoplasms / etiology
  • Risk
  • Triglycerides / blood

Substances

  • Triglycerides