Artigo Revisado por pares

Over Expression of CD44V8—10 in Human Bladder Cancer Cells Decreases Their Interaction With Hyaluronic Acid and Potentiates Their Malignant Progression

2004; Lippincott Williams & Wilkins; Volume: 171; Issue: 1 Linguagem: Inglês

10.1097/01.ju.0000093446.54115.b6

ISSN

1527-3792

Autores

Mototsugu Muramaki, Hideaki Miyake, Sadao Kamidono, Isao Hara,

Tópico(s)

Fibroblast Growth Factor Research

Resumo

No AccessJournal of UrologyINVESTIGATIVE UROLOGY1 Jan 2004Over Expression of CD44V8—10 in Human Bladder Cancer Cells Decreases Their Interaction With Hyaluronic Acid and Potentiates Their Malignant Progression MOTOTSUGU MURAMAKI, HIDEAKI MIYAKE, SADAO KAMIDONO, and ISAO HARA MOTOTSUGU MURAMAKIMOTOTSUGU MURAMAKI , HIDEAKI MIYAKEHIDEAKI MIYAKE , SADAO KAMIDONOSADAO KAMIDONO , and ISAO HARAISAO HARA View All Author Informationhttps://doi.org/10.1097/01.ju.0000093446.54115.b6AboutFull TextPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract Purpose: We evaluated the effects of the over expression of CD44v8–10, one of the high molecular form of CD44, on the malignant potential of UM-UC-3 human bladder cancer cells in vitro and in vivo. Materials and Methods: We introduced CD44v8–10 complementary DNA into UM-UC-3 cells, which do not express detectable level of CD44v8–10 protein, and generated the CD44v8–10 over expressing cell line UM-UC-3/v8–10 and the vector only transfected cell line UM-UC-3/C. The effects of the introduction of CD44v8–10 into UM-UC-3 cells on the ability to bind hyaluronic acid (HA) were analyzed by the cell adhesion assay and the cell migration assay. We then evaluated tumor progression of UM-UC-3 sublines after subcutaneous and orthotopic injection into athymic nude mice. Results: There were no significant differences in in vitro growth rates. UM-UC-3/v8–10 cells showed significantly decreased binding and migration ability to HA but not to other extracellular matrix proteins. Furthermore, UM-UC-3/v8–10 cells demonstrated significantly increased tumor growth after subcutaneous as well as orthotopic injection into athymic nude mice and enhanced lymph node metastasis after orthotopic injection compared with UM-UC-3/C cells. Conclusions: These findings suggest that CD44v8–10 over expression in human bladder cancer cells decreases their interaction with HA and potentiates their malignant progression. References 1 : Natural history of bladder cancer. Prognostic features and long-term disease course. Urol Clin North Am1992; 19: 429. Google Scholar 2 : Recent advances in bladder cancer chemotherapy. Cancer Invest2001; 19: 77. Google Scholar 3 : Interaction between CD44 and hyaluronate is directly implicated in the regulation of tumor development. J Exp Med1994; 180: 53. Google Scholar 4 : Expression of CD44R1 adhesion molecule in colon carcinoma and metastases. Lancet1993; 341: 725. Google Scholar 5 : Restoration of CD44H expression in colon carcinomas reduces tumorigenicity. Ann Surg1995; 222: 493. Google Scholar 6 : CD44 standard form expression as a predictor of progression in high risk superficial bladder tumors. Int Urol Neohrol2001; 33: 479. Google Scholar 7 : Evaluation of clinicopathological factors and the correlation between the adhesion molecule CD44 variant 9 expression and pulmonary metastasis from colorectal cancers. Int Surg2002; 87: 130. Google Scholar 8 : Molecular detection of cancer cells by competitive reverse transcription-polymerase chain reaction analysis of specific CD44 variant RNAs. J Natl Cancer Inst1998; 90: 307. Google Scholar 9 : Over expression of CD44v8–10 in urinary exfoliated cells as an independent prognostic predictor in patients with urothelial cancer. J Urol2002; 167: 1282. Link, Google Scholar 10 : Expression patterns of CD44 adhesion molecule in testicular germ cell tumors and normal testes. Am J Pathol1998; 152: 1157. Google Scholar 11 : CD44 is the principal cell surface receptor for hyaluronate. Cell1990; 61: 1303. Crossref, Medline, Google Scholar 12 : The hematopoietic and epithelial forms of CD44 are distinct polypeptides with different adhesion potentials for hyaluronate-bearing cells. EMBO J1991; 10: 343. Google Scholar 13 : Interaction between CD44 and hyaluronic acid regulates human prostate cancer development. J Urol1998; 160: 1562. Link, Google Scholar 14 : CD44 hyaluronate binding influences growth kinetics and tumorigenicity of human colon carcinomas. Oncogene1995; 11: 2223. Google Scholar 15 : CD44s expression in human colon carcinomas influences growth of liver metastases. Int J Cancer2000; 85: 523. Google Scholar 16 : Hyaluronic acid/CD44H interaction induces cell detachment and stimulates migration and invasion of human glioma cells in vitro. Int J Cancer1995; 63: 450. Google Scholar 17 : Overexpression of Bcl-2 enhances metastatic potential of human bladder cancer cells. Br J Cancer1999; 79: 1651. Google Scholar 18 : High levels of stromal hyaluronan predict poor disease outcome in epithelial ovarian cancer. Cancer Res2000; 60: 150. Google Scholar 19 : Serum hyaluronan (hyaluronic acid) in breast cancer patients. Int J Cancer1990; 46: 388. Google Scholar From the Division of Urology, Department of Organ Therapeutics, Faculty of Medicine, Kobe University Graduate School of Medicine, Kobe and Department of Urology, Hyogo Medical Center for Adults, Akashi, Japan© 2004 by American Urological Association, Inc.FiguresReferencesRelatedDetails Volume 171Issue 1January 2004Page: 426-430 Advertisement Copyright & Permissions© 2004 by American Urological Association, Inc.Keywordsbladder neoplasmsbladderhyaluronic acidantigens, CD44mice, nudeMetricsAuthor Information MOTOTSUGU MURAMAKI More articles by this author HIDEAKI MIYAKE More articles by this author SADAO KAMIDONO More articles by this author ISAO HARA More articles by this author Expand All Advertisement PDF downloadLoading ...

Referência(s)
Altmetric
PlumX