Literature DB >> 6731586

Growth response of B16 melanoma to in vivo treatment with 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) at the initial stage after tumor transplantation.

X H Li, G Paulus, G Atassi, N Buyssens.   

Abstract

The changes of implanted B16 melanoma fragments in situ following early treatment with 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) were studied by quantitative histopathologic methods from Day 1 to Day 7 and at Day 14 after transplantation. During the first 3-day period there were no apparent differences between the two groups in all the parameters studied. The most striking differences were observed on Day 5 after implantation, when the drug-treated tumor showed the lowest number of morphologically intact tumor cells and the lowest level of proliferative capacity, with a high proportion of melanotic cells. The late infiltration of host macrophages was more abundant in drug-treated tumors than in controls due to an enhanced production and liberation of melanin granules. The results suggest that a 7-day growth delay of drug-treated tumors is characterized not only by a reduced number (one order of magnitude) of intact tumor cells but also by a severely suppressed proliferative capacity.

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Year:  1984        PMID: 6731586      PMCID: PMC1900518     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  12 in total

1.  The response of hypoxic B16 melanoma cells to in vivo treatment with chemotherapeutic agents.

Authors:  R P Hill; J A Stanley
Journal:  Cancer Res       Date:  1975-05       Impact factor: 12.701

2.  Duration of drug levels in mice as indicated by residual antileukemic efficacy.

Authors:  I Kline; M Gang; D D Tyrer; N Mantel; J M Venditti; A Goldin
Journal:  Chemotherapia (Basel)       Date:  1968

3.  Giant histiocytes after cyclophosphamide.

Authors:  G Castaldi; G Zavagli; O Fiocchi; F Trotta
Journal:  Experientia       Date:  1970-03-15

4.  The clinical pharmacology of antineoplastic agents (second of two parts).

Authors:  B A Chabner; C E Myers; C N Coleman; D G Johns
Journal:  N Engl J Med       Date:  1975-05-29       Impact factor: 91.245

Review 5.  An elementary introduction to stereology (quantitative microscopy).

Authors:  H Elias; D M Hyde
Journal:  Am J Anat       Date:  1980-12

6.  Spontaneous maturation and differentiation of B16 melanoma cells in culture.

Authors:  J W Kreider; M E Schmoyer
Journal:  J Natl Cancer Inst       Date:  1975-09       Impact factor: 13.506

7.  Suppression of melanoma cell tyrosinase activity and tumorigenicity after incorporation of bromouracil for one or two cell divisions.

Authors:  J R Wrathall; E W Newcomb; R Balint; L Zeitz; S Silagi
Journal:  J Cell Physiol       Date:  1975-12       Impact factor: 6.384

8.  Tumour volume response, initial cell kill and cellular repopulation in B16 melanoma treated with cyclophosphamide and 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea.

Authors:  T C Stephens; J H Peacock
Journal:  Br J Cancer       Date:  1977-09       Impact factor: 7.640

9.  Tumor dormancy in vivo by prevention of neovascularization.

Authors:  M A Gimbrone; S B Leapman; R S Cotran; J Folkman
Journal:  J Exp Med       Date:  1972-08-01       Impact factor: 14.307

10.  Cell yield and cell survival following chemotherapy of the B16 melanoma.

Authors:  T C Stephens; J H Peacock
Journal:  Br J Cancer       Date:  1978-11       Impact factor: 7.640

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  3 in total

1.  The species-specific structure of microanatomical compartments in the human spleen: strongly sialoadhesin-positive macrophages occur in the perifollicular zone, but not in the marginal zone.

Authors:  B Steiniger; P Barth; B Herbst; A Hartnell; P R Crocker
Journal:  Immunology       Date:  1997-10       Impact factor: 7.397

2.  Responses of a murine B16 melanoma to pharmacotherapy studied and compared with different assay systems.

Authors:  Y Kuwashima; O Matsubara; T Kasuga
Journal:  J Cancer Res Clin Oncol       Date:  1990       Impact factor: 4.553

3.  CD8+ T cell concentration determines their efficiency in killing cognate antigen-expressing syngeneic mammalian cells in vitro and in mouse tissues.

Authors:  Sadna Budhu; John D Loike; Ashley Pandolfi; Soo Han; Geoffrey Catalano; Andrei Constantinescu; Raphael Clynes; Samuel C Silverstein
Journal:  J Exp Med       Date:  2010-01-11       Impact factor: 14.307

  3 in total

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