Abstract
The sera from patients with nasopharyngeal carcinoma (n = 30), oral carcinoma (n = 22) and laryngeal carcinoma (n = 22) was extracted before treatment. The concentration of circulating intercellular adhesion molecule 1 (ICAM-1), E-selectin and vascular cell adhesion molecule 1 (VCAM-1) was measured by enzyme-linked immunoassay and compared with those from normal subjects (n = 20). The concentration of circulating ICAM-1, E-selectin and VCAM-1 was significantly increased in nasopharyngeal carcinoma. Correspondingly, VCAM-1 and E-selectin were significantly increased in laryngeal carcinoma, whereas only E-selectin was elevated in oral carcinoma. The concentrations of these adhesion molecules did not significantly differ with respect to the early and late stages of these carcinomas. Elevated levels of soluble adhesion molecules in the sera of cancer patients at three different head and neck regions, although appearing to be implicated in these tumour formations, may be unrelated to tumour progression. © 1999 Cancer Research Campaign
Keywords: circulating adhesion molecule, intercellular adhesion molecule 1, E-selectin, vascular cell adhesion molecule 1, head and neck cancer
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- Azuma A., Yagita H., Matsuda H., Okumura K., Niitani H. Induction of intercellular adhesion molecule 1 on small cell lung carcinoma cell lines by gamma-interferon enhances spontaneous and bispecific anti-CD3 x antitumor antibody-directed lymphokine activated killer cell cytotoxicity. Cancer Res. 1992 Sep 15;52(18):4890–4894. [PubMed] [Google Scholar]
- Banks R. E., Gearing A. J., Hemingway I. K., Norfolk D. R., Perren T. J., Selby P. J. Circulating intercellular adhesion molecule-1 (ICAM-1), E-selectin and vascular cell adhesion molecule-1 (VCAM-1) in human malignancies. Br J Cancer. 1993 Jul;68(1):122–124. doi: 10.1038/bjc.1993.298. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Becker J. C., Dummer R., Hartmann A. A., Burg G., Schmidt R. E. Shedding of ICAM-1 from human melanoma cell lines induced by IFN-gamma and tumor necrosis factor-alpha. Functional consequences on cell-mediated cytotoxicity. J Immunol. 1991 Dec 15;147(12):4398–4401. [PubMed] [Google Scholar]
- Bevilacqua M. P., Nelson R. M. Selectins. J Clin Invest. 1993 Feb;91(2):379–387. doi: 10.1172/JCI116210. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Birdsall H. H., Lane C., Ramser M. N., Anderson D. C. Induction of VCAM-1 and ICAM-1 on human neural cells and mechanisms of mononuclear leukocyte adherence. J Immunol. 1992 May 1;148(9):2717–2723. [PubMed] [Google Scholar]
- Gearing A. J., Newman W. Circulating adhesion molecules in disease. Immunol Today. 1993 Oct;14(10):506–512. doi: 10.1016/0167-5699(93)90267-O. [DOI] [PubMed] [Google Scholar]
- Giavazzi R., Chirivi R. G., Garofalo A., Rambaldi A., Hemingway I., Pigott R., Gearing A. J. Soluble intercellular adhesion molecule 1 is released by human melanoma cells and is associated with tumor growth in nude mice. Cancer Res. 1992 May 1;52(9):2628–2630. [PubMed] [Google Scholar]
- Harning R., Mainolfi E., Bystryn J. C., Henn M., Merluzzi V. J., Rothlein R. Serum levels of circulating intercellular adhesion molecule 1 in human malignant melanoma. Cancer Res. 1991 Sep 15;51(18):5003–5005. [PubMed] [Google Scholar]
- Hsu M. M., Ko J. Y., Chang Y. L. Elevated levels of soluble interleukin 2 receptor and tumor necrosis factor in nasopharyngeal carcinoma. Arch Otolaryngol Head Neck Surg. 1991 Nov;117(11):1257–1259. doi: 10.1001/archotol.1991.01870230073010. [DOI] [PubMed] [Google Scholar]
- Kageshita T., Yoshii A., Kimura T., Ono T. Analysis of expression and soluble form of intercellular adhesion molecule-1 in malignant melanoma. J Dermatol. 1992 Nov;19(11):836–840. doi: 10.1111/j.1346-8138.1992.tb03793.x. [DOI] [PubMed] [Google Scholar]
- Koch A. E., Burrows J. C., Haines G. K., Carlos T. M., Harlan J. M., Leibovich S. J. Immunolocalization of endothelial and leukocyte adhesion molecules in human rheumatoid and osteoarthritic synovial tissues. Lab Invest. 1991 Mar;64(3):313–320. [PubMed] [Google Scholar]
- Kuo W. R., Yu H. S., Chang K. L., Juan K. H., Jan Y. S., Yu C. L. Increased production of tumor necrosis factor-alpha and release of soluble CD4 and CD8 molecules, but decreased responsiveness to phytohemagglutinin in patients with nasopharyngeal carcinoma. J Formos Med Assoc. 1994 Jul;93(7):569–575. [PubMed] [Google Scholar]
- Kuzu I., Bicknell R., Fletcher C. D., Gatter K. C. Expression of adhesion molecules on the endothelium of normal tissue vessels and vascular tumors. Lab Invest. 1993 Sep;69(3):322–328. [PubMed] [Google Scholar]
- Lauri D., Needham L., Martin-Padura I., Dejana E. Tumor cell adhesion to endothelial cells: endothelial leukocyte adhesion molecule-1 as an inducible adhesive receptor specific for colon carcinoma cells. J Natl Cancer Inst. 1991 Sep 18;83(18):1321–1324. doi: 10.1093/jnci/83.18.1321. [DOI] [PubMed] [Google Scholar]
- Maio M., Gulwani B., Langer J. A., Kerbel R. S., Duigou G. J., Fisher P. B., Ferrone S. Modulation by interferons of HLA antigen, high-molecular-weight melanoma associated antigen, and intercellular adhesion molecule 1 expression by cultured melanoma cells with different metastatic potential. Cancer Res. 1989 Jun 1;49(11):2980–2987. [PubMed] [Google Scholar]
- McCarthy J. B., Skubitz A. P., Iida J., Mooradian D. L., Wilke M. S., Furcht L. T. Tumor cell adhesive mechanisms and their relationship to metastasis. Semin Cancer Biol. 1991 Jun;2(3):155–167. [PubMed] [Google Scholar]
- Natali P., Nicotra M. R., Cavaliere R., Bigotti A., Romano G., Temponi M., Ferrone S. Differential expression of intercellular adhesion molecule 1 in primary and metastatic melanoma lesions. Cancer Res. 1990 Feb 15;50(4):1271–1278. [PubMed] [Google Scholar]
- Pigott R., Dillon L. P., Hemingway I. H., Gearing A. J. Soluble forms of E-selectin, ICAM-1 and VCAM-1 are present in the supernatants of cytokine activated cultured endothelial cells. Biochem Biophys Res Commun. 1992 Sep 16;187(2):584–589. doi: 10.1016/0006-291x(92)91234-h. [DOI] [PubMed] [Google Scholar]
- Pizzolo G., Vinante F., Nadali G., Ricetti M. M., Morosato L., Marrocchella R., Vincenzi C., Semenzato G., Chilosi M. ICAM-1 tissue overexpression associated with increased serum levels of its soluble form in Hodgkin's disease. Br J Haematol. 1993 May;84(1):161–162. doi: 10.1111/j.1365-2141.1993.tb03040.x. [DOI] [PubMed] [Google Scholar]
- Price J. T., Bonovich M. T., Kohn E. C. The biochemistry of cancer dissemination. Crit Rev Biochem Mol Biol. 1997;32(3):175–253. doi: 10.3109/10409239709082573. [DOI] [PubMed] [Google Scholar]
- Rice G. E., Bevilacqua M. P. An inducible endothelial cell surface glycoprotein mediates melanoma adhesion. Science. 1989 Dec 8;246(4935):1303–1306. doi: 10.1126/science.2588007. [DOI] [PubMed] [Google Scholar]
- Rice G. E., Munro J. M., Corless C., Bevilacqua M. P. Vascular and nonvascular expression of INCAM-110. A target for mononuclear leukocyte adhesion in normal and inflamed human tissues. Am J Pathol. 1991 Feb;138(2):385–393. [PMC free article] [PubMed] [Google Scholar]
- Rothlein R., Dustin M. L., Marlin S. D., Springer T. A. A human intercellular adhesion molecule (ICAM-1) distinct from LFA-1. J Immunol. 1986 Aug 15;137(4):1270–1274. [PubMed] [Google Scholar]
- Rothlein R., Mainolfi E. A., Czajkowski M., Marlin S. D. A form of circulating ICAM-1 in human serum. J Immunol. 1991 Dec 1;147(11):3788–3793. [PubMed] [Google Scholar]
- Seth R., Raymond F. D., Makgoba M. W. Circulating ICAM-1 isoforms: diagnostic prospects for inflammatory and immune disorders. Lancet. 1991 Jul 13;338(8759):83–84. doi: 10.1016/0140-6736(91)90077-3. [DOI] [PubMed] [Google Scholar]
- Smith M. E., Thomas J. A. Cellular expression of lymphocyte function associated antigens and the intercellular adhesion molecule-1 in normal tissue. J Clin Pathol. 1990 Nov;43(11):893–900. doi: 10.1136/jcp.43.11.893. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tomita Y., Nishiyama T., Watanabe H., Fujiwara M., Sato S. Expression of intercellular adhesion molecule-1 (ICAM-1) on renal-cell cancer: possible significance in host immune responses. Int J Cancer. 1990 Dec 15;46(6):1001–1006. doi: 10.1002/ijc.2910460609. [DOI] [PubMed] [Google Scholar]
- Tsujisaki M., Imai K., Hirata H., Hanzawa Y., Masuya J., Nakano T., Sugiyama T., Matsui M., Hinoda Y., Yachi A. Detection of circulating intercellular adhesion molecule-1 antigen in malignant diseases. Clin Exp Immunol. 1991 Jul;85(1):3–8. doi: 10.1111/j.1365-2249.1991.tb05673.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vánky F., Wang P., Patarroyo M., Klein E. Expression of the adhesion molecule ICAM-1 and major histocompatibility complex class I antigens on human tumor cells is required for their interaction with autologous lymphocytes in vitro. Cancer Immunol Immunother. 1990;31(1):19–27. doi: 10.1007/BF01742491. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wenzel C. T., Scher R. L., Richtsmeier W. J. Adhesion of head and neck squamous cell carcinoma to endothelial cells. The missing links. Arch Otolaryngol Head Neck Surg. 1995 Nov;121(11):1279–1286. doi: 10.1001/archotol.1995.01890110053010. [DOI] [PubMed] [Google Scholar]
- Yamamoto T., Yoneda K., Ueta E., Osaki T. Serum cytokines, interleukin-2 receptor, and soluble intercellular adhesion molecule-1 in oral disorders. Oral Surg Oral Med Oral Pathol. 1994 Dec;78(6):727–735. doi: 10.1016/0030-4220(94)90087-6. [DOI] [PubMed] [Google Scholar]