Literature DB >> 4006052

Decreased retention of vinca alkaloids in chronic lymphatic leukemia cells from refractory patients.

M Beksac, C Peterson, P Reizenstein.   

Abstract

Uptake and retention of vincristine (VCR), vinblastine (VB), and vindesine (VD) in isolated mononuclear cells from six healthy donors and in leukemic cells from 12 patients with chronic lymphatic leukemia (CLL) were studied: Three patients responded to VCR-containing regimens, whereas 4 patients were or became refractory and five patients did not receive VCR. Incubation of leukemic or normal cells with 1 microgram/ml vinca alkaloid for 1-24 h showed a steady state level after 1-2 h. Normal cells both took up and retained significantly more drug than those from patients, both responding and refractory. Cells from VCR-refractory patients had a significantly (P less than 0.01) lower drug retention than those from patients responding to or not receiving VCR. In contrast, the difference in uptake was not statistically significant.

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Year:  1985        PMID: 4006052     DOI: 10.1007/bf00257299

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  13 in total

1.  Uptake and binding of vincristine by murine leukemia cells.

Authors:  W A Bleyer; S A Frisby; V T Oliverio
Journal:  Biochem Pharmacol       Date:  1975-03-01       Impact factor: 5.858

Review 2.  Plant products in cancer chemotherapy.

Authors:  S K Carter; R B Livingston
Journal:  Cancer Treat Rep       Date:  1976-08

3.  Differences in daunomycin retention in sensitive and resistant P388 leukemic cells as determined by digitized video fluorescence microscopy.

Authors:  S Yanovich; R N Taub
Journal:  Cancer Res       Date:  1983-09       Impact factor: 12.701

4.  Circumvention of vincristine and Adriamycin resistance in vitro and in vivo by calcium influx blockers.

Authors:  T Tsuruo; H Iida; M Nojiri; S Tsukagoshi; Y Sakurai
Journal:  Cancer Res       Date:  1983-06       Impact factor: 12.701

5.  Mechanism of cross-resistance between vincristine and daunorubicin in Ehrlich ascites tumor cells.

Authors:  T Skovsgaard
Journal:  Cancer Res       Date:  1978-12       Impact factor: 12.701

6.  Restored in vitro sensitivity of adriamycin- and vincristine-resistant P388 leukemia with reserpine.

Authors:  M Inaba; R Fujikura; S Tsukagoshi; Y Sakurai
Journal:  Biochem Pharmacol       Date:  1981-08-01       Impact factor: 5.858

7.  Cross-resistance of cultured murine leukemia vincristine-resistant P388 cells to vinblastine, vindesine, and bis (N-ethylidene vindesine) disulfide, disulfate.

Authors:  L J Wilkoff; E A Dulmadge
Journal:  J Natl Cancer Inst       Date:  1982-06       Impact factor: 13.506

8.  The mode of action of Vinca alkaloids.

Authors:  O Csuka; J Sugár; I Pályi; S Somfai-Relle
Journal:  Oncology       Date:  1980       Impact factor: 2.935

9.  Establishment of Vincristine-resistant and vindesine-resistant lines of murine lymphoblasts in vitro and characterisation of their patterns of cross-resistance and drug sensitivities.

Authors:  B T Hill; R D Whelan
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

10.  Phase II clinical trial with vindesine for remission induction in acute leukemia, blastic crisis of chronic myeloid leukemia, lymphosarcoma, and hodgkin's disease: absence of cross-resistance with vincristine.

Authors:  G Mathé; J L Misset; F De Vassal; J Gouveia; M Hayat; D Machover; D Belpomme; J L Pico; L Schwarzenberg; P Ribaud; M Musset; C Jasmin; L De Luca
Journal:  Cancer Treat Rep       Date:  1978-05
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  2 in total

1.  Aggressive or non-aggressive tumor therapy.

Authors:  P Reizenstein
Journal:  Med Oncol Tumor Pharmacother       Date:  1986

2.  P-glycoprotein expression in refractory hematological neoplasms and circumvention of resistance with verapamil or cyclosporine A containing protocols.

Authors:  M Beksaç; H Akan; H Koç; O Ilhan; S Ertürk; A Güneyli; Y Ikizünal; O S Sardaş
Journal:  Med Oncol Tumor Pharmacother       Date:  1992
  2 in total

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