Hemoglobin induces colon cancer cell proliferation by release of reactive oxygen species

World J Gastroenterol. 2006 Sep 21;12(35):5644-50. doi: 10.3748/wjg.v12.i35.5644.

Abstract

Aim: To study whether hemoglobin could amplify colon cancer cell proliferation via reactive oxygen species (ROS) production.

Methods: Colon cancer cell line HT-29 was grown in the conventional method using RPMI1640 media. The viability of the cells was measured using the colorimetric MTT [3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide] assay after adding hemoglobin. We determined reactive oxygen species levels to be indicators of oxidative stress in HT 29 cell lines with and without hemoglobin and/or 5-fluorouracil (5-FU), 5'-deoxy-5-fluorouridine (5-DFUR) using fluorometric dichlorofluorescin diacetate (DCFH-DA) assay.

Results: Cellular proliferation was increased with hemoglobin in a concentration-dependent manner. A significant increment on ROS levels was found in HT 29 cells following hemoglobin incubation. The cytotoxic effects of 5-FU and 5-DFUR were significantly blunted by administration of hemoglobin. There was a slight increase of peroxiredoxin 1, superoxide dismutase 1 concentration according to different hemoglobin concentrations.

Conclusion: Hemoglobin has a cellular proliferative effect on HT-29 colon cancer cell line by production of ROS. Also, hemoglobin abates cytotoxic effects of chemotherapeutic agents such as 5-FU and 5-DFUR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimetabolites, Antineoplastic / pharmacology
  • Capecitabine
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology*
  • Deoxycytidine / analogs & derivatives
  • Deoxycytidine / pharmacology
  • Dose-Response Relationship, Drug
  • Fluorouracil / pharmacology
  • Gene Expression Regulation, Neoplastic / drug effects
  • HT29 Cells
  • Hemoglobins / physiology*
  • Humans
  • Oxidative Stress
  • Peroxidases / genetics
  • Peroxidases / metabolism
  • Peroxiredoxins
  • Reactive Oxygen Species / metabolism*
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism

Substances

  • Antimetabolites, Antineoplastic
  • Hemoglobins
  • Reactive Oxygen Species
  • Deoxycytidine
  • Capecitabine
  • Peroxidases
  • PRDX1 protein, human
  • Peroxiredoxins
  • Superoxide Dismutase
  • Fluorouracil