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Carbonic anhydrase-9 (CA9), a transmembrane enzyme with an extracellular active site, is involved in the reversible metabolism of the carbon dioxide to carbonic acid. Up-regulation of CA by hypoxia and the hypoxia-inducible factor (HIF) pathway has been recently postulated (Wykoff et al. Cancer Res., 60: 7075-7083, 2000). In the present study we examined the expression of this enzyme in non-small cell lung cancer. Of 107 cases analyzed, 39 (36.4%) had strong membrane/cytoplasmic expression of CA9 and were grouped as positive. The staining was confined around areas of necrosis, and a significant association of CA9 expression with the extent of necrosis was noted (P = 0.004). Nevertheless, 38 of 74 cases with focal or extensive necrosis did not express CA9. CA9 expression was more frequent in the squamous cell histology (P = 0.001) and with advanced T stage (P = 0.009). A significant coexpression of CA9 with platelet-derived endothelial cell growth factor and basic fibroblast growth factor receptor expression was noted. Double staining of CA9 with anti-CD31 monoclonal antibody revealed an overall higher microvessel density in the areas expressing CA9 than in negative areas (P = 0.0005). Thirty-one of 38 CA9-positive cases were positive for HIF1a/HIF2a, but HIF positivity was a more common event (68 of 107) and their patterns of expression were diffuse (not confined in the necrotic areas). A direct association of CA9 expression with epidermal growth factor receptor, c-erbB-2, and MUC1 expression was also noted (P < 0.04). Survival analysis showed that CA9 expression is related to poor prognosis. CA9 expression in tumors with low vascularization defined a prognosis similar to the one of patients with highly angiogenic tumors. Multivariate analysis revealed that CA9 expression is a significant prognostic factor independent of angiogenesis. We conclude that CA9 is an important molecule in non-small cell lung cancer, the up-regulation of which occurs in highly hypoxic/necrotic regions of the tumors. The expression of CA9 is linked to the expression of a constellation of proteins involved in angiogenesis, apoptosis inhibition, and cell-cell adhesion disruption, which explains the strong association of CA9 with poor outcome.

Type

Journal article

Journal

Cancer Res

Publication Date

01/11/2001

Volume

61

Pages

7992 - 7998

Keywords

Adenocarcinoma, Adult, Aged, Antigens, Neoplasm, Basic Helix-Loop-Helix Transcription Factors, Carbonic Anhydrase IX, Carbonic Anhydrases, Carcinoma, Non-Small-Cell Lung, Carcinoma, Squamous Cell, Cell Hypoxia, Enzyme Induction, Female, Fibroblast Growth Factor 2, Humans, Hypoxia-Inducible Factor 1, alpha Subunit, Lung Neoplasms, Male, Middle Aged, Mucin-1, Necrosis, Neoplasm Proteins, Neovascularization, Pathologic, Prognosis, Receptor, Epidermal Growth Factor, Receptor, ErbB-2, Signal Transduction, Thymidine Phosphorylase, Trans-Activators, Transcription Factors