Volume 172, Issue 3 p. 261-266
Original Paper

Nm23 ‘anti-metastatic’ gene product expression in colorectal carcinoma

Janice A. Royds

Corresponding Author

Janice A. Royds

Department of Pathology, University of Sheffield Medical School, PO Box 596, Sheffield, S10 2UL, U.K.

Department of Pathology, University of Sheffield Medical School, PO Box 596, Sheffield, S10 2UL, U.K.Search for more papers by this author
Simon S. Cross

Simon S. Cross

Department of Pathology, University of Sheffield Medical School, PO Box 596, Sheffield, S10 2UL, U.K.

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Paul B. Silcocks

Paul B. Silcocks

Department of Public Health Medicine, University of Sheffield Medical School, PO Box 596, Sheffield, S10 2UL, U.K.

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John H. Scholefield

John H. Scholefield

Department of Surgery, Northern General Hospital, Herries Road, Sheffield, S5 7AU, U.K.

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Robert C. Rees

Robert C. Rees

Institute of Cancer Studies, University of Sheffield Medical School, PO Box 596, Sheffield, S10 2UL, U.K.

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Timothy J. Stephenson

Timothy J. Stephenson

Department of Pathology, University of Sheffield Medical School, PO Box 596, Sheffield, S10 2UL, U.K.

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First published: March 1994
Citations: 33

Abstract

Nm23 is a putative metastasis suppressor gene and alterations in this gene have been reported in colorectal carcinomas suggestive of a role for nm23 in the dissemination of these tumours. In this study we used an affinity purified polyclonal antibody, ab-11, on formalin-fixed, paraffin-embedded sections of colorectai carcinomas from 46 patients in a three-stage avidin–biotin complex immunoperoxidase technique. Follow-up of these patients was until time of death or for 5 years, with a mean time of 31·2 months. Two observers scored the staining results from 1 to 3 according to the proportion of tumour cells positive. The association of nm23 staining with survival, sex, age, vascular invasion, and Dukes' stage was determined using Cox's regression model. The association of death from colorectal cancer and nm23 status reached marginal significance in this study (P = 0.0417). Moreover, there is some suggestion of a protective effect from nm23 as the relative risk of dying from colorectal cancer for each increment of nm23 positivity is 0·573 (95 per cent confidence limits 0·34–0·98).