Basic Fibroblast Growth Factor Regulates Matrix Metalloproteinases Production and In Vitro Invasiveness in Human Bladder Cancer Cell Lines
1997; Lippincott Williams & Wilkins; Volume: 157; Issue: 6 Linguagem: Inglês
10.1016/s0022-5347(01)64779-7
ISSN1527-3792
AutoresHideaki Miyake, Koji Yoshimura, Isao Hara, Hiroshi Eto, Soichi Arakawa, Sadao Kamidono,
Tópico(s)Epigenetics and DNA Methylation
ResumoNo AccessJournal of UrologyInvestigative Urology1 Jun 1997Basic Fibroblast Growth Factor Regulates Matrix Metalloproteinases Production and In Vitro Invasiveness in Human Bladder Cancer Cell Lines Hideaki Miyake, Koji Yoshimura, Isao Hara, Hiroshi Eto, Soichi Arakawa, and Sadao Kamidono Hideaki MiyakeHideaki Miyake , Koji YoshimuraKoji Yoshimura , Isao HaraIsao Hara , Hiroshi EtoHiroshi Eto , Soichi ArakawaSoichi Arakawa , and Sadao KamidonoSadao Kamidono View All Author Informationhttps://doi.org/10.1016/S0022-5347(01)64779-7AboutFull TextPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract Purpose: This study was designed to investigate the effect of endogenous basic fibroblast growth factor (FGF-2) on matrix metalloproteinases (MMPs) production and in vitro invasive potential of human bladder cancer cell lines. Materials and Methods: The human bladder cancer cell lines, HT1376 and KoTCC-1, were used in this study. The mRNA for FGF receptor has been shown to be expressed in both cell lines; the mRNA for FGF-2 is expressed in only KoTCC-1. The effects of FGF-2 expression on HT1376 by gene transfection and those of FGF-2 antisense oligonucleotides treatment on KoTCC-1 were analyzed by zymography and in vitro tumor cell invasion assay. Results: The introduction of human FGF-2 gene into HT1376 cells markedly enhanced both the MMP-2 and MMP-9 production, and the in vitro invasive potential was also increased. In contrast, the exposure of KoTCC-1 cells to FGF-2 specific antisense oligonucleotides decreased the MMP-2 production and in vitro invasive potential, but the exposure to FGF-2 sense oligonucleotides did not. Conclusions: These findings suggest that FGF-2 plays an important role in the invasive process of human bladder cancer in part through the regulation of MMPs production. References 1 : Current management of invasive and metastatic transitional cell carcinoma of the bladder. J. Urol.1993; 149: 957. Link, Google Scholar 2 : Contemporary cystectomy with pelvic node dissection compared to preoperative radiation therapy plus cystectomy in management of invasive bladder cancer. J. Urol.1984; 131: 1069. Link, Google Scholar 3 : Preliminary results of M-VAC (methotrexate, vinblastine, doxorubicin and cisplatin) for transitional cell carcinoma of the urotherium. J. Urol.1985; 133: 403. Abstract, Google Scholar 4 : Introduction of basic fibroblast growth factor gene into mouse renal cell carcinoma cell line enhances its metastatic potential. Cancer Res.1996; 56: 2440. Google Scholar 5 : Angiogenic factors. Science1987; 235: 442. Crossref, Medline, Google Scholar 6 : Elevated levels of the angiogenic peptide basic fibroblast growth factor in urine of bladder cancer patients. J. Natl. Cancer Inst.1993; 85: 241. Crossref, Medline, Google Scholar 7 : Expression of basic fibroblast growth factor and its receptor in an invasive bladder carcinoma cell line. J. Cell. Physiol.1993; 155: 368. Google Scholar 8 : Tumor invasion and metastasis: an imbalance of positive and negative regulation. Cancer Res.1991; 51: 5054s. Google Scholar 9 : Degradation and basement membrane type IV collagen and lung subendotherial matrix by rat mammary adenocarcinoma cell clones of differing metastatic potentials. Cancer Res.1987; 47: 4869. Google Scholar 10 : Serum and plasma Mr 92,000 progelatinase levels correlate with spontaneous metastasis of rat 13762NF mammary adenocarcinoma. Cancer Res.1993; 53: 5802. Google Scholar 11 : Messenger RNA for two type IV collagenases is located in stromal cells in human colon cancer. Am. J. Pathol.1993; 142: 359. Google Scholar 12 : Type IV collagenase (Mr 72,000) expression in human prostate: benign and malignant tissue. Cancer Res.1993; 53: 878. Medline, Google Scholar 13 : Levels of matrix metalloproteinase in bladder cancer correlate with tumor grade and invasion. Cancer Res.1993; 53: 5365. Google Scholar 14 : Secreted or nonsecreted forms of acidic fibroblast growth factor produced by transfected epithelial cells influence cell morphology, motility, and invasive potential. Proc. Natl. Acad. Sci. USA1991; 88: 2893. Google Scholar 15 : A minority of carcinoma cells producing acidic fibroblast growth factor induces a community effect for tumor progression. Proc. Natl. Acad. Sci. USA1994; 91: 286. Google Scholar 16 : Tumor invasion and extracellular matrix degradative enzymes: regulation of activity by organ factors. Semin. Cancer Biol.1991; 2: 115. Google Scholar 17 : Regulation of gelatinase production in metastatic renal cell carcinoma by organ-specific fibroblasts. Jpn. J. Cancer Res.1994; 85: 152. Google Scholar 18 : Human bladder carcinoma: characterization of two new tumor cell lines and search for tumor viruses. J. Natl. Cancer Inst.1977; 58: 881. Google Scholar 19 : Expression and secretion of the beta subunit of human chorionic gonadotropin by bladder carcinoma in vitro. Cancer Res.1995; 55: 1479. Google Scholar 20 : Messenger ribonucleic acids for fibroblast growth factors and their receptor in human bladder and renal cell carcinoma cell lines. Cancer Lett.1996; 103: 91. Google Scholar 21 : Transformation of mouse BALA/c 3T3 cells with human basic fibroblast growth factor cDNA. Mol. Cell. Biol.1988; 8: 588. Google Scholar 22 : Cloning and expression of cDNA encoding human basic fibroblast growth factor. FEBS Lett.1987; 213: 189. Google Scholar 23 : Phosphorothioate antisense oligonucleotides against basic fibroblast growth factor inhibited anchorage-dependent and anchorage-independent growth of a malignant glioblastoma cell line. Mol. Endo.1992; 16: 877. Google Scholar 24 : A sensitive enzyme immunoassay for human basic fibroblast growth factor. Biochem. Biophys. Res. Commun.1991; 175: 229. Google Scholar 25 : Influence of organ environment on extracellular matrix degradation activity and metastasis of human colon carcinoma cells. J. Natl. Cancer Inst.1990; 82: 1890. Google Scholar 26 : A rapid in vitro assay for quantitating the invasive potential of tumor cells. Cancer Res.1987; 47: 3239. Medline, Google Scholar 27 : Type IV collagenases in tumor invasion and metastasis. Cancer Metast. Rev.1990; 9: 289. Google Scholar 28 : Isolation and characterization of metastatic variants from human transitional cell carcinoma passaged by orthotopic implantation in athymic nude mice. J. Urol.1995; 154: 1532. Link, Google Scholar 29 : Influence of growth factors on in vitro invasiveness and type IV collagenolysis of human renal cell carcinoma cells. J. Urol.1994; 151: 223. Google Scholar 30 : Suppression of solid tumor growth by immunoneutralizing monoclonal antibody against human basic fibroblast growth factor. Cancer Res.1991; 51: 6180. Google Scholar 31 : Inhibition of cell growth and tumorigenesis of human glioblastoma cells by a neutralizing antibody against human basic fibroblast growth factor. FEBS Lett.1991; 288: 65. Google Scholar 32 : Cell motility, invasion, and malignancy induced by overexpression of K-FGF or bFGF. Exp. Cell Res.1993; 204: 295. Google Scholar From the Department of Urology, Kobe University School of Medicine, Kobe, Japan.© 1997 by American Urological Association, Inc.FiguresReferencesRelatedDetailsCited byYoussef R, von Rundstedt F, Kapur P, Mosbah A, Abol-Enein H, Ghoneim M and Lotan Y (2014) Utility of Biomarkers in the Prediction of Oncologic Outcome after Radical Cystectomy for Squamous Cell CarcinomaJournal of Urology, VOL. 193, NO. 2, (451-456), Online publication date: 1-Feb-2015.MIYAKE H, ETO H, HARA I, SO A, LI D and GLEAVE M (2018) SYNERGISTIC ANTITUMOR ACTIVITY BY COMBINED TREATMENT WITH GEMCITABINE AND ANTISENSE OLIGODEOXYNUCLEOTIDE TARGETING CLUSTERIN GENE IN AN INTRAVESICAL ADMINISTRATION MODEL AGAINST HUMAN BLADDER CANCER KOTCC-1 CELLSJournal of Urology, VOL. 171, NO. 6 Part 1, (2477-2481), Online publication date: 1-Jun-2004.MUNRO N and KNOWLES M (2018) Fibroblast Growth Factors and Their Receptors in Transitional Cell CarcinomaJournal of Urology, VOL. 169, NO. 2, (675-682), Online publication date: 1-Feb-2003.HARA I, MIYAKE H, HARA S, ARAKAWA S and KAMIDONO S (2018) SIGNIFICANCE OF MATRIX METALLOPROTEINASES AND TISSUE INHIBITORS OF METALLOPROTEINASE EXPRESSION IN THE RECURRENCE OF SUPERFICIAL TRANSITIONAL CELL CARCINOMA OF THE BLADDERJournal of Urology, VOL. 165, NO. 5, (1769-1772), Online publication date: 1-May-2001.MENDELSOHN J and DINNEY C (2018) THE WILLET F. 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