Granulocyte colony-stimulating factor receptor signals for β 1-integrin expression and adhesion in bladder cancer

Urology

Volumn 63, Issue 1, 2004, Pages 177-183

  Chakraborty, Arup ^a   White, Scott M ^b   Lerner, Seth P ^b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BETA1 INTEGRIN; FIBRONECTIN; GRANULOCYTE COLONY STIMULATING FACTOR; GRANULOCYTE COLONY STIMULATING FACTOR RECEPTOR; LAMININ;

ARTICLE; AUTOCRINE EFFECT; BLADDER CARCINOMA; CANCER CELL CULTURE; CANCER INVASION; CANCER TISSUE; CARCINOMA CELL; CELL ADHESION; CONTROLLED STUDY; CYSTECTOMY; DISEASE ASSOCIATION; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; METASTASIS; MOLECULAR DYNAMICS; NEUTROPHIL; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SAMPLE; STATISTICAL SIGNIFICANCE; UPREGULATION; UROTHELIUM; WESTERN BLOTTING;

EID: 0742272158     PISSN: 00904295     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0090-4295(03)00786-6     Document Type: Article

References (22)

1. Morini M., Mottolese M., Ferrari N., et al. The alpha 3 beta 1 integrin is associated with mammary carcinoma cell metastasis, invasion, and gelatinase b (mmp-9) activity. Int J Cancer. 87:2000;336-342.
2. Skubitz A.P. Adhesion molecules. Cancer Treat Res. 107:2002;305-329.
3. Yamada K.M., Kennedy D.W., Yamada S.S., et al. Monoclonal antibody and synthetic peptide inhibitors of human tumor cell migration. Cancer Res. 50:1990;4485-4496.
4. Fujita S., Suzuki H., Kinoshita M., et al. Inhibition of cell attachment, invasion and metastasis of human carcinoma cells by anti-integrin beta 1 subunit antibody. Jpn J Cancer Res. 83:1992;1317-1326.
5. Tachibana M., Murai M. G-CSF production in human bladder cancer and its ability to promote autocrine growth a review . Cytokines Cell Mol Ther. 4:1998;113-120.
6. Ohigashi T., Tachibana M., Tazaki H., et al. Bladder cancer cells express functional receptors for granulocyte-colony stimulating factor. J Urol. 147:1992;283-286.
7. Tkatch L.S., Tweardy D.J. Human granulocyte colony-stimulating factor (G-CSF), the premier granulopoietin biology, clinical utility, and receptor structure and function . Lymphokine Cytokine Res. 12:1993;477-488.
8. Chakraborty A., Hentzen E.R., Seo S.M., et al. Granulocyte colony-stimulating factor promotes adhesion of neutrophils. Am J Physiol Cell Physiol. 284:2003;C103-C110.
9. 2 (CD11b/CD18) expression by cytokines is regulated by Stat3-dependent activation of pu.1. J Biol Chem. 277:2002;19001-19007.
10. Yong K.L. Granulocyte colony-stimulating factor (G-CSF) increases neutrophil migration across vascular endothelium independent of an effect on adhesion comparison with granulocyte-macrophage colony-stimulating factor (GM-CSF) . J Am Assoc Gynecol Laparosc. 8:2001;267-271.
11. White S.M., Ball E.D., Ehmann W.C., et al. Increased expression of the differentiation-defective granulocyte colony-stimulating factor receptor mRNA isoform in acute myelogenous leukemia. Leukemia. 12:1998;899-906.
12. Lawrence M.B., Smith C.W., Eskin S.G., et al. Effect of venous shear stress on CD18-mediated neutrophil adhesion to cultured endothelium. Blood. 75:1990;227-237.
13. Tweardy D.J., Wright T.M., Ziegler S.F., et al. Granulocyte colony-stimulating factor rapidly activates a distinct STAT-like protein in normal myeloid cells. Blood. 86:1995;4409-4416.
14. Sunaga H., Fujieda S., Tsuzuki H., et al. Expression of granulocyte colony-stimulating factor receptor and platelet-derived endothelial cell growth factor in oral and oropharyngeal precancerous lesions. Anticancer Res. 21:2001;2901-2906.
15. Savarese T.M., Mitchell K., McQuain C., et al. Coexpression of granulocyte colony stimulating factor and its receptor in primary ovarian carcinomas. Cancer Lett. 162:2001;105-115.
16. Hirai K., Kumakiri M., Fujieda S., et al. Expression of granulocyte colony-stimulating factor and its receptor in epithelial skin tumors. J Dermatol Sci. 25:2001;179-188.
17. Kyo S., Kanaya T., Takakura M., et al. A case of cervical cancer with aggressive tumor growth possible autocrine growth stimulation by G-CSF and IL-6 . Gynecol Oncol. 78:2000;383-387.
18. Ichiishi E., Yoshikawa T., Kogawa T., et al. Possible paracrine growth of adenocarcinoma of the stomach induced by granulocyte colony stimulating factor produced by squamous cell carcinoma of the oesophagus. Gut. 46:2000;432-434.
19. Mercurio A.M., Bachelder R.E., Rabinovitz I., et al. The metastatic odyssey the integrin connection . Surg Oncol Clin North Am. 10:2001;313-328.
20. Mizejewski G.J. Role of integrins in cancer survey of expression patterns . Proc Soc Exp Biol Med. 222:1999;124-138.
21. Bohle A., Jurczok A., Ardelt P., et al. Inhibition of bladder carcinoma cell adhesion by oligopeptide combinations in vitro and in vivo. J Urol. 167:2002;357-363.
22. Syrigos K.N., Harrington K.J., Pignatelli M. Role of adhesion molecules in bladder cancer an important part of the jigsaw . Urology. 53:1999;428-434.