Skip to main content

Advertisement

Log in

T-antigen expression by peanut agglutinin staining relates to mucosal dysplasia in ulcerative colitis

  • Published:
Diseases of the Colon & Rectum

Abstract

Staining of 326 rectal mucosal biopsies from ulcerative colitis patients with peanut agglutinin (PNA), which binds to the T-blood group antigen and has been claimed to reflect a cancer-associated mucin alteration, showed highly significant direct associations with mucosal dysplasia (P<0.001), disease activity (P<0.001), and subsequent development of rectal cancer in a smaller series of patients (P=0.005). Staining for normal colonic mucin by theDolichos biflorus (DBA) lectin related significantly and inversely to dysplasia. Intense normal colon mucin staining by DBA related significantly (P<0.025) to long disease duration and to subsequent development of cancer (P=0.02). The latter association is based on a small number of patients only and is not considered conclusive evidence, but may provide a link with goblet-cell hyperplasia. The authors conclude that although T-antigen expression relates to dysplasia, the findings of “false” positive and negative rates of 22 and 33 percent respectively, make it unlikely that staining of biopsy sections for the T-antigen by peanut agglutinin will contribute materially to routine assessment for dysplasia and cancer risk prediction in patients with ulcerative colitis.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Morson BC, Pang LS. Rectal biopsy as an aid to cancer control in ulcerative colitis. Gut 1967;8:423–34.

    Article  CAS  Google Scholar 

  2. Craft CF, Mendelsohn G, Cooper HS. Colonic “precancer” in Crohn's disease. Gastroenterology 1981;80:578–84.

    Article  CAS  Google Scholar 

  3. Lennard-Jones JE, Morson BC, Ritchie JK, Shove DC, Williams BM. Cancer in colitis: assessment of the individual risk by clinical and histological criteria. Gastroenterology 1977;73:1280–9.

    Article  CAS  Google Scholar 

  4. Johnson WR, McDermott FT, Hughes ESR, Milne BJ, Pihl EA, Price AB. Carcinoma of the colon and rectum in inflammatory disease of the intestine. Surg Gynecol Obstet 1983;156:193–7.

    CAS  PubMed  Google Scholar 

  5. Johnson WR, McDermott FT, Pihl E, Hughes ES. Mucosal dysplasia: a major predictor of cancer following ileorectal anastomosis. Dis Colon Rectum 1983;26:697–700.

    Article  CAS  Google Scholar 

  6. Riddell RH, Goldman H, Ransohoff DF, et al. Dysplasia in inflammatory bowel disease: standardized classification with provisional clinical applications. Hum Pathol 1983;14:931–68.

    Article  CAS  Google Scholar 

  7. Boland CR, Montgomery CK, Kim YS. Alterations in human colonic mucin occurring with cellular differentiation and malignant transformation. Proc Natl Acad Sci USA 1982;79:2051–5.

    Article  CAS  Google Scholar 

  8. Cooper HS. Peanut lectin-binding sites in large bowel carcinoma: peanut lectin-binding sites in large bowel carcinoma. Lab Invest 1982;47:383–90.

    CAS  PubMed  Google Scholar 

  9. Johnson WR, McDermott FT, Hughes ES, Pihl EA, Milne BJ, Price AB. The risk of rectal carcinoma following colectomy in ulcerative colitis. Dis Colon Rectum 1983;26:44–6.

    Article  CAS  Google Scholar 

  10. Morson BC, Dawson IM. Gastrointestinal pathology Oxford: Blackwell, 1976.

    Google Scholar 

  11. Sokal RR, Rohlf FJ. Biometry: the principles and practice of statistics in biological research. San Francisco. WM Freeman & Co, 1969.

    Google Scholar 

  12. Kaplan EL, Meier P. Nonparametric estimation from incomplete observations. J Am Statist Assoc 1958;53:457–81.

    Article  Google Scholar 

  13. Gehan EA. A generalized Wilcoxon test for comparing arbitrarily singly censored samples. Biometrika 1965;52:203–23.

    Article  CAS  Google Scholar 

  14. Rampal P, La Mont JT, Trier JS. Differentiation of glycoprotein synthesis in fetal rat colon. Am J Physiol 1978;235:E207.

    CAS  PubMed  Google Scholar 

  15. La Mont JT, Ventola A. Galactosyltransferase in fetal, neonatal, and adult colon: relationship to differentiation. Am J Physiol 1978;235:E213–7.

    Google Scholar 

  16. Boland CR, Montgomery CK, Kim YS. A cancer-associated mucin alteration in benign colonic polyps. Gastroenterology, 1982;82:664–72.

    Article  CAS  Google Scholar 

  17. Cooper HS, Reuter UE. Peanut lectin-binding sites in polyps of the colon and rectum: adenomas, hyperplastic polyps, and adenomas with in situ carcinoma. Lab Invest 1983;49:655–61.

    CAS  PubMed  Google Scholar 

  18. Lotan R, Skutelsky E, Danor D, Skaron N. The purification, composition, and specificity of the anti-T lectin from peanut (Arachis hypogaea). J Biol Chem 1975;250:8518–23.

    Article  CAS  Google Scholar 

  19. Hakomori S, Kannagi R. Glycosphingolipids as tumor-associated and differentiation markers. J Natl Cancer Inst 1983;71:231–50.

    CAS  PubMed  Google Scholar 

  20. Springer GF, Desai PR, Murphy MS, Yang HJ, Scanlan EF. Precursors of the blood group MN antigens as human carcinoma associated antigens. Transfusion 1979;19:233–49.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported by a grant from the Alfred Hospital.

About this article

Cite this article

Pihl, E., Peura, A., Johnson, W.R. et al. T-antigen expression by peanut agglutinin staining relates to mucosal dysplasia in ulcerative colitis. Dis Colon Rectum 28, 11–17 (1985). https://doi.org/10.1007/BF02553898

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02553898

Key words

Navigation