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Serum YKL-40 and colorectal cancer
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  • Open Access
  • Published: 26 February 1999

Serum YKL-40 and colorectal cancer

  • C Cintin1,
  • J S Johansen2,
  • I J Christensen3,
  • P A Price4,
  • S Sørensen5 &
  • …
  • H J Nielsen1 

British Journal of Cancer volume 79, pages 1494–1499 (1999)Cite this article

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Summary

YKL-40 is a mammalian member of the chitinase protein family. Although the function of YKL-40 is unknown, the pattern of its expression suggests a function in remodelling or degradation of extracellular matrix. High serum YKL-40 has been found in patients with recurrent breast cancer and has been related to short survival. In the present study we analysed YKL-40 in preoperative sera from patients with colorectal cancer and evaluated its relation to survival. Serum YKL-40 was determined by RIA in 603 patients. Survival after operation was registered, and median follow-up time was 61 months. Three hundred and forty patients died. Sixteen per cent of the patients with Dukes’ A, 26% with Dukes’ B, 19% with Dukes’ C and 39% with Dukes’ D had high serum YKL-40 levels (adjusted for age). Analysis of serum YKL-40 as a continuous variable showed an association between increased serum YKL-40 and short survival (P < 0.0001). Patients with high preoperative serum YKL-40 concentration had significantly shorter survival than patients with normal YKL-40 (HR = 1.7; 95% CI: 1.3–2.1, P < 0.0001). Multivariate Cox analysis including serum YKL-40, serum CEA, Dukes’ stage, age and gender showed that high YKL-40 was an independent prognostic variable for short survival (HR = 1.4; 95% CI: 1.1–1.8, P = 0.007). These results suggest that YKL-40 may play an important role in tumour invasion.

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

References

  • Bresalier, R. S., Byrd, J. C., Wang, L. & Raz, A. (1996). Colon cancer mucin: a new ligand for the β-galactoside-binding protein galectin-3. Cancer Res, 56: 4354–4357.

    CAS  PubMed  Google Scholar 

  • Dukes, C. & Bussey, H. J. R. (1958). The spread of rectal cancer and its effect on prognosis. Br J Cancer 12: 309–320.

    Article  CAS  Google Scholar 

  • Finlay, I. & McArdle, C. S. (1983). Effect of occult hepatic metastases on survival after curative resection for colorectal carcinoma. Gastroenterology 85: 596–599.

    CAS  PubMed  Google Scholar 

  • Hakala, B. E., White, C. & Recklies, A. D. (1993). Human cartilage gp-39, a major secretory product of articular chondrocytes and synovial cells, is a mammalian member of a chitinase protein family. J Biol Chem, 268: 5803–5810.

    Google Scholar 

  • Hu, B., Trinh, K., Figueira, W. F. & Price, P. A. (1996). Isolation and sequence of a novel human chondrocyte protein related to mammalian members of the chitinase protein family. J Biol Chem 271: 19415–19420.

    Article  CAS  Google Scholar 

  • Jass, J. R., Love, S. B. & Northover, J. M. (1987). A new prognostic classification of rectal cancer. Lancet, 1: 1303–1306.

    Article  CAS  Google Scholar 

  • Johansen, J. S., Williamson, M. K., Rice, J. S. & Price, P. A. (1992). Identification of proteins secreted by human osteoblastic cells in culture. J Bone Miner Res, 7: 501–512.

    Article  CAS  Google Scholar 

  • Johansen, J. S., Jensen, H. S. & Price, P. A. (1993). A new biochemical marker for joint injury. Analysis of YKL-40 in serum and synovial fluid. Br J Rheumatol, 32: 949–955.

    Article  CAS  Google Scholar 

  • Johansen, J. S., Cintin, C., Jørgensen, M., Kamby, C. & Price, P. A. (1995). Serum YKL-40: a new potential marker of prognosis and location of metastases of patients with recurrent breast cancer. Eur J Cancer, 31A: 1437–1442.

    Article  CAS  Google Scholar 

  • Johansen, J. S., Hvolris, J., Hansen, M., Backer, V., Lorenzen, I. & Price, P. A. (1996). Serum YKL-40 levels in healthy children and adults. Comparison with serum and synovial fluid levels of YKL-40 in patients with osteoarthritis or trauma of the knee joint. Br J Rheumatol, 35: 553–559.

    Article  CAS  Google Scholar 

  • Kievit, J. & Van de Velde, C. J. H. (1990). Utility and cost of carcinoembryonic antigen monitoring in colon cancer follow-up evaluation. Cancer, 65: 2580–2587.

    Article  CAS  Google Scholar 

  • Kirkpatrick, R. B., Emery, J. G., Connor, J. R., Dodds, R., Lysko, P. G. & Rosenberg, M. (1997). Induction and expression of human cartilage glycoprotein 39 in rheumatoid inflammatory and peripheral blood monocyte-derived macrophages. Exp Cell Res 237: 46–54.

    Article  CAS  Google Scholar 

  • Krause, S. W., Rehli, M., Kreutz, M., Schwarzfischer, L., Paulauskis, J. D. & Andreesen, R. (1996). Differential screening identifies genetic markers of monocyte to macrophage maturation. J Leukoc Biol 60: 540–545.

    Article  CAS  Google Scholar 

  • Lucha, P. A., Rosen, L., Olenwine, J. A., Reed, J. F., Riether, R. D., Stasik, J. J. & Khubchandani, I. T. (1997). Value of carcinoembryonic antigen monitoring in curative surgery for recurrent colorectal carcinoma. Dis Colon Rectum, 40: 145–149.

    Article  Google Scholar 

  • McArdle, C. S., Hole, D., Hansell, D., Blumgart, L. H. & Wood, C. B. (1990). Prospective study of colorectal cancer in the West of Scotland: 10 year follow-up. Br J Surg, 77: 280–282.

    Article  CAS  Google Scholar 

  • Morrison, B. W. & Leder, P. (1994). neu and ras initiate murine mammary tumors that share genetic markers generally absent in c-myc and int-2-initiated tumors. Oncogene 9: 3417–3426.

    CAS  PubMed  Google Scholar 

  • Newland, R. C., Chapuis, P. H. & Smyth, E. J. (1987). The prognostic value of substaging colorectal carcinoma. A prospective study of 1117 cases with standardized pathology. Cancer, 60: 852–857.

    Article  CAS  Google Scholar 

  • Nielsen, H. J., McArdle, C. S. & Moesgaard, F. The RANX05 Study Group (1998). The effect of ranitidine on long-term survival in primary colorectal cancer. G I Cancer, 2: 227–233.

    Google Scholar 

  • Nyirkos, P. & Golds, E. E. (1990). Human synovial cells secrete a 39 kDa protein similar to a bovine mammary protein expressed during the non-lactating period. Biochem J, 268: 265–268.

    Article  Google Scholar 

  • Raz, A., Zhu, D., Hogan, V., Shah, N., Raz, T., Karkash, R., Pazerine, G. & Carmi, P. (1990). Evidence for the role of 34-kDa galactoside-binding lectin in transformation and metastasis. Int J Cancer, 46: 871–877.

    Article  CAS  Google Scholar 

  • Rehli, M., Krause, S. W. & Andreesen, R. (1997). Molecular characterization of the gene for human cartilage gp-39 (CHI3L1), a member of the chitinase protein family and marker for late stages of macrophage differentiation. Genomics, 43: 221–225.

    Article  CAS  Google Scholar 

  • Renkema, G. H., Boot, G. R., Au, F. L., Donker-Koopman, W. E., Strijland, A., Muijsers, A. O., Hrebicek, M. & Aerts, JMFG (1998). Chitotriosidase, a chitinase, and the 39-kDa human cartilage glycoprotein, a chitin-binding lectin, are homologues of family 18 glycosyl hydrolases secreted by human macrophages. Eur J Biochem, 251: 504–509.

    Article  CAS  Google Scholar 

  • Royston, P. (1991). Constructing time-specific reference ranges. Statist Med, 10: 675–690.

    Article  CAS  Google Scholar 

  • Shoeppner, H. L., Raz, A., Ho, S. B. & Bresalier, R. S. (1995). Expression of an endogenous galactose-binding lectin correlates with neoplastic progression in the colon. Cancer, 75: 2818–2826.

    Article  Google Scholar 

  • Shackelton, L. M., Mann, D. M. & Millis, A. J. T. (1995). Identification of a 38-kDa heparin binding glycoprotein (gp38k) in differentiating vascular smooth muscle cells as a member of a group of proteins associated with tissue remodeling. J Biol Chem, 270: 13076–13083.

    Article  CAS  Google Scholar 

  • Skjak-Braek, G., Anthonsen, T. & Sandford, P. A. (1989). Chitin and Chitosan: Sources, Chemistry, Biochemistry, Physical Properties and Applications, Elsevier Applied Science: New York

    Google Scholar 

  • Ståhle, E., Glimelius, B., Bergstrom, R. & Pahlman, L. (1989). Preoperative prediction of outcome in patients with rectal and rectosigmoid cancer. Cancer, 63: 1831–1837.

    Article  Google Scholar 

  • Virgo, K. S., Vernava, A. M., Longo, W. E., McKirgan, L. W. & Johnson, F. E. (1995). Cost of patient follow-up after potentially curative colorectal cancer treatment. JAMA, 23: 1837–1841.

    Article  Google Scholar 

  • Volck, B., Price, P. A., Johansen, J. S., Sørensen, O., Benfield, T., Nielsen, H. J., Calafat, J. & Borregaard, N. (1998). YKL-40, a mammalian member of the bacterial chitinase family, is a matrix protein of specific granules in human neutrophils. Proc Assoc Am Phys, 110: 351–360.

    CAS  PubMed  Google Scholar 

  • Wiggers, T., Arends, J. W., Schutte, B. & Volovics Bosman, F. T. (1988). A multivariate analysis of pathological prognostic indicators in large bowel cancer. Cancer, 61: 386–395.

    Article  CAS  Google Scholar 

  • Wojciechowitcz, D. C., Park, P. Y. & Baty, P. B. (1995). β1–6 branching of N-linked carbohydrate is associated with K-ras mutation in human colon carcinoma cell lines. Biochem Biophys Res Commun, 212: 758–766.

    Article  Google Scholar 

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Authors and Affiliations

  1. Department of Surgical Gastroenterology, Hvidovre Hospital, University of Copenhagen, Denmark

    C Cintin & H J Nielsen

  2. Department of Rheumatology, Hvidovre Hospital, University of Copenhagen, Denmark

    J S Johansen

  3. The Finsen Laboratory, Rigshospitalet, University of Copenhagen, Denmark

    I J Christensen

  4. Department of Biology, University of California San Diego, La Jolla, California, USA

    P A Price

  5. Department of Clinical Biochemistry, University of Copenhagen, Hvidovre Hospital, University of Copenhagen, Denmark

    S Sørensen

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  1. C Cintin
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Additional information

*YKL-40 has been named after its molecular weight (40 kDa) and the one letter code for its three N-terminal amino acids (Johansen et al, 1992). The protein is also called human cartilage glycoprotein-39 (HC gp-39) (Hakala et al, 1993)

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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Cintin, C., Johansen, J., Christensen, I. et al. Serum YKL-40 and colorectal cancer. Br J Cancer 79, 1494–1499 (1999). https://doi.org/10.1038/sj.bjc.6690238

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  • Received: 20 May 1998

  • Revised: 30 September 1998

  • Accepted: 14 October 1998

  • Published: 26 February 1999

  • Issue Date: 01 March 1999

  • DOI: https://doi.org/10.1038/sj.bjc.6690238

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Keywords

  • carcinoembryonic antigen
  • colorectal cancer
  • metastasis
  • tumour invasiveness
  • YKL-40/HC gp-39

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