CD44H plays an important role in peritoneal dissemination of scirrhous gastric cancer cells

Japanese Journal of Cancer Research

Volumn 87, Issue 12, 1996, Pages 1235-1244

  Nishimura, Shigehiko ^a   Chung, Yong Suk ^a   Yashiro, Masakazu ^a   Inoue, Tohru ^a   Sowa, Michio ^a  

^a OSAKA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Adhesion; CD44H; Mesothelial cell; Peritoneal dissemination; Scirrhous gastric cancer

Indexed keywords

CELL ADHESION MOLECULE; COLLAGEN TYPE 1; FIBRONECTIN; HERMES ANTIGEN; HYALURONIC ACID; MONOCLONAL ANTIBODY;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ANTIGEN EXPRESSION; ARTICLE; CANCER CELL CULTURE; CANCER INVASION; CELL ADHESION; CONTROLLED STUDY; FEMALE; FLOW CYTOMETRY; HUMAN; HUMAN CELL; IMMUNOBLOTTING; MESOTHELIUM CELL; METASTASIS; MOUSE; NONHUMAN; PERITONEUM ADHESION; PRIORITY JOURNAL; STOMACH CANCER;

EID: 0030455652     PISSN: 09105050     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1349-7006.1996.tb03138.x     Document Type: Article

References (31)

1. Tahara, E. Growth factors and oncogenes in human gastrointestinal carcinomas. J. Cancer Res. Clin. Oncol., 116, 121-131 (1990).
2. Sowa, M., Kato, Y., Nishimura, M., Yoshino, H., Kubo, T. and Umeyama, K. Clinicohistochemical studies on type 4 carcinoma of the stomach - with special reference to mucopolysaccharides and sialic acid in tumor tissue. Jpn. J. Surg., 19, 153-162 (1989).
3. Birbeck, M. S. C. and Wheatley, D. N. An electron microscopic study of the invasion of ascites tumor cells into the abdominal wall. Cancer Res., 25, 490-497 (1965).
4. Kimura, A., Koga, S., Kudoh, H. and Iitsuka, Y. Peritoneal mesothelial cell injury factors in rat cancerous ascites. Cancer Res., 45, 4330-4333 (1985).
5. Kiyasu, Y., Kaneshima, S. and Koga, S. Morphogenesis of peritoneal dissemination in human gastric cancer. Cancer Res., 41, 1236-1239 (1981).
6. Kaneshima, S., Kudo, H., Kosaka, H., Iitsuka, Y., Kimachi, H., Takeuchi, T. and Koga, S. A scanning electron microscopic study on implantation of Ehrlich ascites tumor cells in the peritoneal layer. Yonago Acta Med., 20, 101-107 (1976).
7. Cannistra, S. A., Kansas, G. S., Niloff, J., DeFranzo, B., Kim, Y. and Ottensmeier, C. Binding of ovarian cancer cells to peritoneal mesothelium in vivo is partly mediated by CD44H. Cancer Res., 53, 3830-3838 (1993).
8. Hamura, Y., Ito, A., Okada, Y. and Mori, Y. Hyaluronic acid metabolism in inflamed mesenterium of guinea pig. Res. Commun. Chem. Pathol. Pharmacol., 66, 311-327 (1989).
9. Leak, L. V. Interaction of the peritoneal cavity to intraperitoneal stimulation. A peritoneal model system to monitor cellular and extracellular events in the formation of granulation tissue. Am. J. Anat., 173, 171-183 (1985).
10. Jalkanen, S., Bargatze, R. F., de Los Toyos, J. and Butcher, E. C. Lymphocyte recognition of high endothelium: antibodies to distinct epitopes of an 85-95kD glycoprotein antigen differentially inhibit lymphocyte binding to lymph node, mucosal, or synovial endothelial cells. J. Cell Biol., 105, 983-990 (1987).
11. Hoffman, M., Rudy, W., Zoller, M., Tolg, C., Ponta, H., Herrlich, P. and Gunther, U. CD44 splice variants confer metastatic behavior in rats; homologous sequences are expressed in human tumor cell lines. Cancer Res., 51, 5292-5297 (1991).
12. Thomas, L., Byers, H.R., Vink, J. and Stamenkovic, I. CD44H regulates tumor cell migration on hyaluronate-coated substrate. J. Cell Biol., 118, 971-977 (1992).
13. Yashiro, M., Chung, Y. S., Nishimura, S., Inoue, T. and Sowa, M. Peritoneal metastatic model for human scirrhous gastric carcinoma in nude mice. Clin. Exp. Metastasis, 14, 43-54 (1996).
14. Yashiro, M., Chung, Y. S., Nishimura, S. and Sowa, M. Establishment of two new scirrhous gastric cancer cell lines: analysis of factors associated with disseminated metastasis. Br. J. Cancer, 72, 1200-1210 (1995).
15. Laemmli, U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature, 227, 680-685 (1970).
16. Jonjic, N., Peri, G., Bernasconi, S., Sciacca, F. L., Colotta, F., Pelicci, P. G., Lanfrancone, L. and Mantovani, A. Expression of adhesion molecules and chemotactic cytokines in cultured human mesothelial cells. J. Exp. Med., 176, 1165-1174 (1992).
17. Rice, G. E., Munro, J. M. and Bevilacqua, P. B. Inducible cell adhesion molecule 110 (INCAM-110) is an endothelial receptor for lymphocytes. A CD11/CD18-independent adhesion mechanism. J. Exp. Med., 171, 1369-1374 (1990).
18. Dustin, M. L., Rothlein, R., Bhan, A. K., Dinarello, C. A. and Springer, T. A. Induction by IL 1 and interferon-γ: tissue distribution, biochemistry, and function of a natural adherence molecule (ICAM-1). J. Immunol., 137, 245-254 (1986).
19. Stupack, D. G., Stewart, S., Carter, W. G., Wayner, E. A. and Wilkins, J. A. B lymphocyte fibronectin receptors: expression and utilization. Scand. J. Immunol., 34, 761-769 (1991).
20. Kleinman, H. K., McGarvey, M. L., Hassell, J. R., Star, V. L., Cannon, F. B., Laurie, G. W. and Martin, G. R. Basement membrane complexes with biological activity. Biochemistry, 25, 312-318 (1986).
21. Albini, A., Iwamoto, Y., Kleinman, H. K., Martin, G. R., Aaronson, S. A., Kozlowski, J. M. and McEwan, R. N. A rapid in vitro assay for quantitating the invasive potential of tumor cells. Cancer Res., 47, 3239-3245 (1987).
22. Washington, K., Gottfried, M. R. and Telen, M. J. Expression of the cell adhesion molecule CD44 in gastric adenocarcinomas. Hum. Pathol., 25, 1043-1049 (1994).
23. Gunthert, U., Hoffman, M., Rudy, W., Reber, S., Zoller, M., Haussmann, I., Matzku, S., Wenzel, A., Ponta, H. and Herrlich, P. A new variant of glycoprotein CD44 confers metastatic potential to rat carcinoma cells. Cell, 65, 13-25 (1991).
24. Stamenkovic, I., Aruffo, A., Amiot, M., and Seed, B. The hematopoietic and epithelial forms of CD44 are distinct polypeptides with different adhesion potentials for hyaluronate-bearing cells. EMBO J., 10, 343-348 (1991).
25. Screaton, G.R., Bell, M. V., Jackson, D. G., Cornelis, F. B., Gerth, U. and Bell, J. I. Genomic structure of DNA encoding the lymphocyte homing receptor CD44 reveals at least 12 alternatively spliced exons. Proc. Natl. Acad. Sci. USA, 89, 12160-12164 (1992).
26. Merzak, A., Koocheckpour, S. and Pilkington, G. J. CD44 mediates human glioma cell adhesion and invasion in vitro. Cancer Res., 54, 3988-3992 (1994).
27. Cooper, D. L., Dougherty, G., Harn, H. J., Jackson, S., Baptist, E. W., Byers, J., Datta, A., Phillips, G. and Isola, N. R. The complex CD44 transcriptional unit; alternative splicing of three internal exons generates the epithelial form of CD44. Biochem. Biophys. Res. Commun., 182, 569-578 (1992).
28. Heider, K. H., Hofmann, M., Hors, E., van den Berg, F., Ponta, H., Herrlich, P. and Pals, S. T. A human homologue of the rat metastasis-associated variant of CD44 is expressed in colorectal carcinomas and adenomatous polyps. J. Cell Biol., 120, 227-233 (1993).
29. Tanabe, K. K., Ellis, L. M. and Saya, H. Expression of CD44R1 adhesion molecule in colon carcinomas and metastasis. Lancet, 341, 725-726 (1993).
30. Jalkanen, S. and Jalkanen, M. Lymphocyte CD44 binds the COOH-terminal heparin-binding domain of fibronectin. J. Cell Biol., 116, 817-825 (1992).
31. Faassen, A. E., Mooradian, D. L., Tranquille, R. T., Dickinson, R. B., Letourneau, P. C., Oegema, T. R. and McCarthy, J. B. Cell surface CD44-related chondroitin sulfate proteoglycan is required for transforming growth factor-β-stimulated mouse melanoma cell motility and invasive behavior on type I collagen. J. Cell Sci., 105, 501-511 (1993).