Literature DB >> 2293912

Sensitivity to thermochemotherapy of AKR lymphoma and B16 melanoma variants of malignancy.

J Leibovici1, G Klorin, M Huszar, S Hoenig, O Klein, M Michowitz, A Pinchassov.   

Abstract

Drug resistance, which so often accompanies tumor progression, has been shown to be related to changes in membrane properties which may result in decreased drug accumulation in the tumor cell. A correlation between sensitivity to thermochemotherapy and degree of malignancy was found in the AKR lymphoma system. Hyperthermia increased adriamycin (ADR) uptake and concomitantly its cytotoxicity to AKR lymphoma cells. Moreover, these effects were more pronounced on a variant of high malignancy (HM) than on a low malignancy (LM) one. Fluorescent microscopy, as well as cytofluorometry, indicated that lymphoma cells treated by ADR at 43 degrees C were more permeable to the cytotoxic agent than those exposed to the chemotherapeutic substance at 37 degrees C. Cytofluorometry indicated the presence of a minor cell subpopulation with low ADR uptake in the HM variant, not found in the LM one. Fluorocytometry also showed that the temperature-dependent increased ADR uptake was more marked in the HM than in the LM variant, explaining the differential effect of thermochemotherapy on the two lymphoma variants. However, correlation between degree of malignancy and sensitivity to thermochemotherapy is not a general feature. In contrast to the results obtained in the AKR lymphoma system, in the B16 melanoma the low malignancy variant, F1, was more markedly affected by the combined treatment than the F10 variant. The increased cytotoxic effect of ADR by supranormal temperatures in the F1 variant was shown to be due to an augmented drug uptake. The results suggest that drug resistance in late stages of tumor progression can be overcome by an agent acting on the cell membrane. However, the data also indicate the necessity of assaying cancer treatment modalities, including those designed to circumvent drug resistance, on various tumor system models.

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Year:  1990        PMID: 2293912     DOI: 10.1007/bf00155591

Source DB:  PubMed          Journal:  Clin Exp Metastasis        ISSN: 0262-0898            Impact factor:   5.150


  28 in total

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Authors:  B C Giovanella; J S Stehlin; A C Morgan
Journal:  Cancer Res       Date:  1976-11       Impact factor: 12.701

2.  Uptake and retention of daunomycin by mouse leukemic cells as factors in drug response.

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Journal:  Cancer Res       Date:  1968-05       Impact factor: 12.701

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Journal:  Int J Cancer       Date:  1979-02       Impact factor: 7.396

4.  Induction of a tumor with greatly increased metastatic growth potential by injection of cells from a low-metastatic H-2 heterozygous tumor cell line into an H-2 incompatible parental strain.

Authors:  R S Kerbel; R R Twiddy; D M Robertson
Journal:  Int J Cancer       Date:  1978-11-15       Impact factor: 7.396

5.  Clonal drift of cell surface, melanogenic, and experimental metastatic properties of in vivo-selected, brain meninges-colonizing murine B16 melanoma.

Authors:  K M Miner; T Kawaguchi; G W Uba; G L Nicolson
Journal:  Cancer Res       Date:  1982-11       Impact factor: 12.701

Review 6.  Animal models for tumor progression (short review).

Authors:  J Leibovici; M Wolman
Journal:  Anticancer Res       Date:  1984 May-Jun       Impact factor: 2.480

7.  Serial passage of tumors in mice in the study of tumor progression and testing of antineoplastic drugs.

Authors:  J Leibovici
Journal:  Cancer Res       Date:  1984-05       Impact factor: 12.701

8.  Active efflux of daunorubicin and adriamycin in sensitive and resistant sublines of P388 leukemia.

Authors:  M Inaba; H Kobayashi; Y Sakurai; R K Johnson
Journal:  Cancer Res       Date:  1979-06       Impact factor: 12.701

9.  Direct antitumor effect of high-molecular-weight levan on Lewis lung carcinoma cells in mice.

Authors:  J Leibovici; G Susskind-Brudner; M Wolman
Journal:  J Natl Cancer Inst       Date:  1980-08       Impact factor: 13.506

10.  Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. analysis and examples.

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Journal:  Br J Cancer       Date:  1977-01       Impact factor: 7.640

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  2 in total

1.  Effect of hyperthermia and thermochemotherapy on primary and metastatic tumour cells of AKR lymphoma.

Authors:  G Klorin; A Siegal; B Bar-Shira-Maymon; O Klein; J Leibovici
Journal:  Int J Exp Pathol       Date:  1990-08       Impact factor: 1.925

2.  Malignant phenotype correlating with drug resistance in two human neuroblastoma cell lines.

Authors:  Y Wollman; I Shahar; M Goldstein; J Leibovici
Journal:  J Neurooncol       Date:  1994       Impact factor: 4.130

  2 in total

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