Endogenous markers of hypoxia/anaerobic metabolism and anemia in primary colorectal cancer

Cancer Sci. 2006 Jul;97(7):582-8. doi: 10.1111/j.1349-7006.2006.00220.x.

Abstract

Anemia has been implicated in the decreased oxygen tension noted within the tumor environment. In a series of 79 colorectal adenocarcinomas we investigated the role of anemia in activating molecular pathways regulated by hypoxia. Preoperative Hb levels were correlated with the immunohistochemical expression of HIF1alpha and HIF2alpha, LDH5, GLUT1, VEGF, DEC1 and BNIP3, and with angiogenesis and the cancer cell proliferation index. Upregulation of HIF1alpha and HIF2alpha proteins, found in 43% and 44.3% of cases, respectively, was not related to anemia (Hb < 10 g%). This is in agreement with other studies suggesting that HIF activation occurs for various reasons, such as poor or irregular vascularity, or oncogene activation. Nevertheless, low Hb levels (<10 g%) were linked to activated anaerobic metabolism (LDH5 overexpression) in a subset of tumors not expressing HIF1alpha (P < 0.01). Overexpression of HIFs, whether linked to anemia or not, was associated with a number of factors related to tumor aggressiveness (assessed as local invasion and nodal metastasis), anaerobic metabolism and intratumoral acidosis (LDH5, GLUT1; increased glucose metabolism to lactate), activation of genes related to necrosis (BNIP3) and angiogenesis (VEGF). Expression of BNIP3 emerged as the strongest independent factor related to transmural invasion and metastasis to lymph nodes. Identification of specific patterns of the hypoxia molecular cascade activated in cancer cells might help in developing specific therapeutic policies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / complications
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology*
  • Anaerobiosis
  • Anemia / diagnosis*
  • Anemia / etiology
  • Anemia / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / analysis*
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Biomarkers, Tumor / analysis*
  • Biomarkers, Tumor / metabolism
  • Cell Cycle Proteins / analysis
  • Cell Cycle Proteins / metabolism
  • Colorectal Neoplasms / complications
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology*
  • Glucose Transporter Type 1 / analysis
  • Glucose Transporter Type 1 / metabolism
  • Humans
  • Hypoxia / diagnosis*
  • Hypoxia / etiology
  • Hypoxia / metabolism
  • Hypoxia-Inducible Factor 1, alpha Subunit / analysis*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Immunohistochemistry
  • Isoenzymes / analysis
  • Isoenzymes / metabolism
  • L-Lactate Dehydrogenase / analysis
  • L-Lactate Dehydrogenase / metabolism
  • Lactate Dehydrogenase 5
  • Membrane Proteins / analysis
  • Membrane Proteins / metabolism
  • Neovascularization, Pathologic / metabolism
  • Oncogene Proteins / analysis
  • Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins / analysis
  • Proto-Oncogene Proteins / metabolism
  • Tumor Suppressor Proteins / analysis
  • Tumor Suppressor Proteins / metabolism
  • Up-Regulation
  • Vascular Endothelial Growth Factor A / analysis
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • BNIP3 protein, human
  • Basic Helix-Loop-Helix Transcription Factors
  • Biomarkers, Tumor
  • Cell Cycle Proteins
  • DELEC1 protein, human
  • Glucose Transporter Type 1
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Isoenzymes
  • MCTS1 protein, human
  • Membrane Proteins
  • Oncogene Proteins
  • Proto-Oncogene Proteins
  • SLC2A1 protein, human
  • Tumor Suppressor Proteins
  • Vascular Endothelial Growth Factor A
  • endothelial PAS domain-containing protein 1
  • L-Lactate Dehydrogenase
  • Lactate Dehydrogenase 5