Chemotherapy of carcinoma of the prostate and testis : experimental study in vivo and in vitro

Prostate cancer: Considering the stagnation in chemotherapy of prostate cancer in recent years, the following experiments were carried out to determine their clinical value. Surgical specimens from 6 patients, 2 permanent cell lines (EB 33 and PC 93) originated from human prostate cancer and a tumor...

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Bibliographische Detailangaben
Veröffentlicht in:Hinyokika kiyo. Acta urologica Japonica. - 1962. - 34(1988), 11 vom: 01. Nov., Seite 1911-6
1. Verfasser: Okada, K (VerfasserIn)
Weitere Verfasser: Kanamaru, H, Yoshiki, T, Hashimura, T, Nishimura, K, Hida, S, Nishio, Y, Oishi, K, Yoshida, O, Yamauchi, T
Format: Aufsatz
Sprache:Japanese
Veröffentlicht: 1988
Zugriff auf das übergeordnete Werk:Hinyokika kiyo. Acta urologica Japonica
Schlagworte:English Abstract Journal Article Antineoplastic Agents Cytarabine 04079A1RDZ Bleomycin 11056-06-7 Peplomycin 56H9L80NIZ Vincristine mehr... 5J49Q6B70F Vinblastine 5V9KLZ54CY Etoposide 6PLQ3CP4P3 Cisplatin Q20Q21Q62J Fluorouracil U3P01618RT Methotrexate YL5FZ2Y5U1
Beschreibung
Zusammenfassung:Prostate cancer: Considering the stagnation in chemotherapy of prostate cancer in recent years, the following experiments were carried out to determine their clinical value. Surgical specimens from 6 patients, 2 permanent cell lines (EB 33 and PC 93) originated from human prostate cancer and a tumor line serially transplanted in nude mice (PC-NCC) were subjected to chemosensitivity tests such as human tumor cloning assay (HTCA) and/or in vivo tumor growth curve experiments using nude mice. The possible chemosensitive drugs screened by using surgical specimens and PC-NCC tumor were cisplatinum (CDDP), bleomycin (BLM), 5-FU, vincristine (VCR), adriamycin (ADM) and methotrexate (MTX). Most of these drugs were also judged as "effective" by HTCA using a permanent cell line. The minimal discrepancy among them may lead to the conclusion that an in vitro assay using a cell line can substitute for the assay using surgical specimens which can not be obtained frequently. Partly based on the data obtained a chemotherapy regimen, VPM-CisCF, consisting of VCR, peplomycin, MTX, CDDP, cytosine arabinoside (Ara-C) and 5-FU, was designed. The effectiveness of this regimen was demonstrated experimentally. Testis cancer: Two different lines of experiments were performed. A human testicular cancer serially transplanted in nude mice was repeatedly exposed to CDDP in vivo to obtain hyposensitivity to this drug. The synergistic effect of CDDP and VP-16 was demonstrated in the tumor thus obtained. One of its mechanisms has been suggested by partial accumulation of cancer cells in the G1-S and G2-M phase in which CDDP exerts its potential effect.(ABSTRACT TRUNCATED AT 250 WORDS)
Beschreibung:Date Completed 19.05.1989
Date Revised 19.11.2015
published: Print
Citation Status MEDLINE
ISSN:0018-1994