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Efficacy of selective estrogen receptor modulators in nude mice bearing human transitional cell carcinoma.

Efficacy of selective estrogen receptor modulators in nude mice bearing human transitional cell carcinoma. Research Abstract Details 

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  • Efficacy of selective estrogen receptor modulators in nude mice bearing human transitional cell carcinoma. Abstract Text:

    guru sonpavdeGuru Sonpavde,norihiko okunoNorihiko Okuno,heidi weissHeidi Weiss,jiang yuJiang Yu,steven s shenSteven S Shen,mamoun younesMamoun Younes,weiguo jianWeiguo Jian,seth p lernerSeth P Lerner,carolyn l smithCarolyn L Smith,

    OBJECTIVES: To evaluate estrogen receptors as a therapeutic target for human bladder cancer. METHODS: The ability of the selective estrogen receptor modulators (SERMs) tamoxifen and raloxifene to inhibit 5637 human transitional cell carcinoma cell proliferation was determined in vitro and in xenograft studies using 5637 cells in female athymic BALB/c nu/nu mice. RESULTS: Treatment with tamoxifen, raloxifene, or the pure antiestrogen ICI 182,780 inhibited proliferation of 5637 cells in vitro. In the first xenograft study, raloxifene (10, 100, or 1000 microg/day) administered by oral gavage inhibited the growth of tumors compared with placebo or untreated controls (P <0.05). In a second experiment, tamoxifen (8.3, 125, or 1250 microg/day) delivered by time-release pellet inhibited tumor growth compared with placebo-treated controls (P <0.01). A comparison study in which tamoxifen (8.3 or 125 microg/day) or raloxifene (100 microg/day) was administered by slow-release pellet demonstrated that both SERMs reduced growth compared to placebo-treated controls (P <0.05), with comparable effectiveness. There was no detectable tumor in 17 of 30 treated mice. In all studies, average tumor volumes in SERM-treated animals declined over the course of treatment. CONCLUSIONS: Selective estrogen receptor modulators inhibit the growth of 5637 transitional cell carcinoma cell xenografts, supporting the rationale to evaluate these agents as targeted therapeutics for patients with urothelial carcinoma.

    Efficacy of selective estrogen receptor modulators in nude mice bearing human transitional cell carcinoma. Publishing Authors By Initials

    g sonpavdeG Sonpavde,n okunoN Okuno,h weissH Weiss,j yuJ Yu,ss shenSS Shen,m younesM Younes,w jianW Jian,sp lernerSP Lerner,cl smithCL Smith,

    For similar neoplasms: neoplasms by site: urogenital neoplasms research abstracts see: neoplasms: neoplasms by site: urogenital neoplasms research

    PUBMED ID PMID:

    MEDLINE DATE:

    Efficacy of selective estrogen receptor modulators in nude mice bearing human transitional cell carcinoma. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Urology

    VOLUME: 69

    Page Numbers: 1221-6

    Journal Abbreviation: Urology

    ISSN: 1527-9995

    DAY: 3

    MONTH: Jun

    YEAR: 2007

    Efficacy of selective estrogen receptor modulators in nude mice bearing human transitional cell carcinoma. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 366151

    Efficacy of selective estrogen receptor modulators in nude mice bearing human transitional cell carcinoma. Keywords Mesh Terms:

    KEYWORDS: Urogenital Neoplasms

    MESH TERMS: drug therapy

    Chemical & Substance for Abstract: Efficacy of selective estrogen receptor modulators in nude mice bearing human transitional cell carcinoma. Information

    Substance Name: Raloxifene

    Registry Number: 84449-90-1

    Grant and Affiliation Information for Efficacy of selective estrogen receptor modulators in nude mice bearing human transitional cell carcinoma.

    AFFILIATION: U.S. Oncology Research, Webster, Texas, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: P20 CA103698

    ACRONYM: CA

    MEDLINETA: Urology

    REFSOURCE:

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