eISSN: 1897-4309
ISSN: 1428-2526
Contemporary Oncology/Współczesna Onkologia
Current issue Archive Manuscripts accepted About the journal Supplements Addendum Special Issues Editorial board Abstracting and indexing Subscription Contact Instructions for authors Ethical standards and procedures
SCImago Journal & Country Rank
3/2004
vol. 8
 
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abstract:

Effect of cyclophosphamide on tumorogenesis of the IL-6 and Hyper-IL-6 gene modified murine melanoma cells

Andrzej Mackiewicz
,
Dariusz Iżycki
,
Katarzyna Baksalary-Iżycka
,
Katarzyna Gryska
,
Maria Łaciak
,
Sergiusz Nawrocki

Współcz Onkol (2004) vol. 8: 3 (124-131)
Online publish date: 2004/04/22
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Background: The study was aimed at evaluating the effect of cyclophosphamide on the melanogenesis of the IL-6 and hyper-IL-6 gene modified murine melanoma cells.
Animals and Experimental Design: Sixty-three (n=63), six-week-old C57/Bl6xC3H chimeric mice were injected with ”wild” type or with interleukin-6 (IL-6) or Hyper-6 (H6) gene modified B-78 murine melanoma cells and/or cyclophosphamide. Control groups were injected s.c. with ”wild” type (group I; n=7), IL-6 (group II; n=7), or H-6 (group III; n=7) gene modified B-78 murine melanoma cells (5x105 cells). In the experimental groups IA, IIA, and IIIA animals were intraperitoneally (i.p.) injected with cyclophosphamide (100 mg/kg) two days before inoculation of B-78 (group IA; n=7), B-78/IL-6 (group IIA; n=7) and
B-78/H6 (group IIIA; n=7) melanoma cells (s.c.; 5x105 cells). In the experimental groups IB (n=7), IIB (n=7) and IIIB (n=7) combined treatment of B-78, B-78/IL-6
and B-78/H6 (respectively; s.c.;
5x105 cells) and cyclophosphamide
(500 mg/kg; i.p., two days before inoculation of B-78 cells) was applied. We evaluated the kinetics of the tumor growth, mean survival time of the animals and immune response. The non-specific (NK cells) immunotoxicity as well as Th1/Th2 and Tc1/Tc2 shift were analyzed by flow cytometry.
Results: The kinetics of the tumor growth study revealed significantly important inhibition of tumor growth in group III mice (day 35, <20 cm3) treated with B-78/H6 mono-therapy. Application of combined B-78/IL-6 and B-78/H6 with cyclophosphamide (100 mg/kg; group IIIA) treatment resulted in significant extension of the survival and tumor growth inhibition.
Flow cytometric analysis of the non-specific cytotoxicity showed no significant difference between control and experimental groups as well as in the Th1/Th2 and Tc1/Tc2 ratios.
Conclusions: Application of low doses of cyclophosphamide resulted in inhibition of the potency of tumor to grow in vivo.
keywords:

cyclophosphamide, gene therapy, melanoma malignum

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