Hypoxia-regulated Carbonic Anhydrase-9 (CA9) Relates to Poor Vascularization and Resistance of Squamous Cell Head and Neck Cancer to Chemoradiotherapy

  1. Michael I. Koukourakis1,
  2. Alexandra Giatromanolaki,
  3. Efthimios Sivridis,
  4. Konstantinos Simopoulos,
  5. Jaromir Pastorek,
  6. Charles C. Wykoff,
  7. Kevin C. Gatter and
  8. Adrian L. Harris
  1. Tumour and Angiogenesis Research Group, Departments of Radiotherapy/Oncology, Pathology and Surgery, Democritus University of Thrace, Alexandroupolis 68100, Greece [M. I. K., A. G., E. S., K. S.]; Institute of Virology, Slovak Academy of Sciences, Bratislava, Slovak Republic, 84246 [J. P.]; and Departments of Cellular Science and Institute of Molecular Medicine, Oxford Radcliffe Hospital, Headington, Oxford, OX3 9DS, United Kingdom [C. C. W., K. C. G., A. L. H.]

    Abstract

    Purpose: Carbonic anhydrases are proteins involved in the catalytic hydration of carbon dioxide to carbonic acid. Recent studies show that carbonic anhydrase 9 (CA9) is up-regulated by hypoxia and that its immunohistochemical tissue distribution follows the distribution of the radiosensitizer pimonidazole (C. C. Wykoff et al., Cancer Res. 60: 7075–7083, 2001). Therefore, CA9 expression may show hypoxia levels of clinical importance.

    Experimental Design: We assessed the expression of CA9 and the microvessel density (MVD; CD31-positive) in 75 locally advanced squamous cell head and neck cancers treated with concurrent chemoradiotherapy with carboplatin.

    Results: Strong membrane/cytoplasmic CA9 expression, noted in 20/75 (26.6%) tumors, mainly occurred in tumors with very poor vascularization (expression in 63% versus 14%; P < 0.0001), was located around areas of focal necrosis, and was related to poor complete response rate (40% versus 70%; P = 0.02). These observations suggested that CA9 might be a marker of clinically important hypoxia. Combining the CA9 staining and the tumor angiogenicity (MVD), we identified three groups of patients: (a) hypoxic tumors; (b) euoxic highly angiogenic tumors; and (c) euoxic non-highly angiogenic tumors. Groups (a) and (b) had a very poor local relapse-free survival (P < 0.0001).

    Conclusions: Stratification of patients undergoing radical radiotherapy using the CA9/MVD model may be useful for the individualization of therapeutic strategies combining antiangiogenesis and hypoxia targeting with radiotherapy.

    Footnotes

    • The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    • 1 To whom requests for reprints should be addressed, at Tumour and Angiogenesis Research Group, 18 Dimokratias Avenue, Iraklion 71306, Crete, Greece. Phone: 0030-932-480808; Fax: 0030-81-284661; E-mail: targ{at}her.forthnet.gr

    • 2 The abbreviations used are: HIF, hypoxia-inducible factor; CA9, carbonic anhydrase 9; SCHNC; squamous cell head and neck carcinoma; APAAP, alkaline phosphatase/antialkaline phosphatase; MVD, microvessel density; LRFS, local relapse-free survival; OS, overall survival.

    • 3 Internet address: www.graphpad.com.

    • 4 A. Giatromanolaki, M. I. Koukourakis, E. Sivridis, J. Pastorek, C. C. Wykoff, K. C. Gatter, A. L. Harris. Expression of hypoxia inducible carbonic anhydrase (CA9) relates to angiogenic pathways and independently to poor outcome in non-small cell lung cancer. Cancer Res., in press, 2001.

      • Accepted July 31, 1901.
      • Received April 27, 1901.
      • Revision received June 28, 1901.
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