Diabetes-associated angiotensin activation enhances liver metastasis of colon cancer

Clin Exp Metastasis. 2012 Dec;29(8):915-25. doi: 10.1007/s10585-012-9480-6. Epub 2012 May 3.

Abstract

We examined the effects of hyperglycemic conditions on liver metastasis of colorectal cancer (CRC). Angiotensin (A)-II increased growth, invasion, and anti-apoptotic survival in HT29 and CT26 cells. In contrast, angiotensinogen (ATG) increased these features in HT29 cells but not in CT26 cells. HT29 cells expressed A-II type 1 receptor, chymase, and rennin, whereas CT26 cells did not express renin. Renin expression and ATG-induced cell growth, invasion, and survival induced and increased as glucose concentration increased in HT29 cells and also CT26 cells. An inhibitor of renin or chymase abrogated A-II production in HT29 cells. Reduction of hepatic ATG production by cholesterol-conjugated antisense S-oligodeoxynucleotide suppressed liver metastasis of HT29 cells. An examination of 121 CRC patients showed that diabetes in CRC cases was associated with higher blood HbA1c, higher renin and A-II concentrations in the primary tumors, and higher incidence of liver metastasis than in nondiabetic cases. These results suggest that diabetes-associated angiotensin activation enhances liver metastasis of CRC and may therefore provide a possible target for antimetastatic therapy in CRC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin I / biosynthesis
  • Angiotensin I / metabolism
  • Angiotensin II / biosynthesis
  • Angiotensin II / metabolism*
  • Angiotensin II Type 1 Receptor Blockers
  • Angiotensinogen / genetics
  • Angiotensinogen / metabolism
  • Animals
  • Apoptosis
  • Cell Line, Tumor
  • Cell Proliferation
  • Chymases / biosynthesis
  • Chymases / genetics
  • Chymases / metabolism
  • Colonic Neoplasms / complications
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • Diabetes Complications / metabolism*
  • Diabetes Mellitus / metabolism*
  • Glucose / analysis
  • Glycated Hemoglobin / analysis
  • HT29 Cells
  • Humans
  • Hyperglycemia
  • Liver Neoplasms / secondary*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasm Invasiveness
  • Oligoribonucleotides, Antisense
  • RNA Interference
  • RNA, Small Interfering
  • Receptor, Angiotensin, Type 1 / metabolism
  • Renin / genetics
  • Renin / metabolism

Substances

  • Angiotensin II Type 1 Receptor Blockers
  • Glycated Hemoglobin A
  • Oligoribonucleotides, Antisense
  • RNA, Small Interfering
  • Receptor, Angiotensin, Type 1
  • hemoglobin A1c protein, human
  • Angiotensinogen
  • Angiotensin II
  • Angiotensin I
  • Chymases
  • Renin
  • Glucose