Advanced search×

In-vitro toxicity of Ukrain against human Ewing tumor cell lines.

Anticancer Drugs 17(9):1025-30 (2006) PMID 17001175

Ukrain is advertised by the manufacturer as a drug for alternative cancer cures with high activity against progressive Ewing tumors. Using the MTT assay, we compared the cytotoxicity of Ukrain with the cytotoxicity of N,N',N''-triethylenethiophosphoramide (thioTEPA), Chelidonium majus L. alkaloids, doxorubicin, cyclophosphamide and etoposide against four human Ewing tumor cell lines. In addition, we studied the cytotoxicity of thioTEPA combined with C. majus L. alkaloids after 48, 72 and 96 h. All compounds reduced the growth of Ewing tumor cell lines in a dose-dependent manner. The concentrations that reduced cell growth by 50% ranged between 6.2 and 31.1 micromol/l for Ukrain, 1.9 and 26.1 micromol/l for C. majus L. extract, and 1.7 and 448 micromol/l for thioTEPA. The sensitivity profile of Ukrain was comparable to that of the C. majus L. alkaloids, and different from that of thioTEPA, cyclophosphamide, etoposide and doxorubicin. Overall, doxorubicin was the most cytotoxic drug followed by cyclophosphamide. Ukrain and the C. majus L. alkaloids were slightly more cytotoxic than etoposide, while thioTEPA showed the lowest cytotoxicity. Co-exposure of thioTEPA with C. majus L. alkaloids resulted in additive but not in synergistic cytotoxicity. The in-vitro results indicate that the cytotoxicity of Ukrain against Ewing tumors is comparable to that of etoposide. While the latter can be used on the basis of broad clinical experience and known risk-benefit ratio, Ukrain for the present might be considered as a candidate for subsequent drug development by xenograft studies followed by systematic clinical trials.

DOI: 10.1097/01.cad.0000231467.61911.50
Version: za2963e q8zad q8zbb q8zc9 q8zd2 q8zec q8zf2 q8zge

Similar articles you may find interesting…

  1. A dynamic multi-organ-chip for long-term cultivation and substance testing proven by 3D human liver and skin tissue co-culture.

    Lab Chip (2013) PMID 23648632

    We present a multi-organ-chip capable of maintaining 3D tissues derived from cell lines, primary cells and biopsies of various human organs. We designed a multi-organ-chip with co-cultures of human artificial liver microtissues and skin biopsies, each a (1)/100 000 of the biomass of their original...
  2. Inhibiting PD-1 pathway rescues M. tuberculosis specific IFN-γ producing T cells from apoptosis in tuberculosis patients.

    J Infect Dis (2013) PMID 23661793

    Background. Over expression of Programmed death-1 (PD-1) receptor is thought to inhibit effector T cell response in human tuberculosis. However, the precise mechanism of such inhibition remains unclear. The present study aimed at addressing the role of PD-1 in dampening host T cell...
  3. The C-terminal module IV of connective tissue growth factor is a novel immune modulator of the Th17 response.

    Lab Invest (2013) PMID 23648563

    Our aim was to explore whether CCN2(IV) could regulate the Th17 response. In vitro, stimulation of human naive CD4(+) T lymphocytes with CCN2(IV) resulted in differentiation to Th17 phenotype. The in vivo effects of CCN2(IV) were studied in C57BL/6 mice. Intraperitoneal administration of recombinant...