Literature DB >> 3243324

Autoradiographic characterization of newly developed melanoic cell group different from the melanoic tumor piece embedded into a liver lobe of mice.

Y Momose1, Y Mabuchi, A Shigematsu.   

Abstract

Secondary proliferous melanoic tumors grew at 100% of probability in a liver lobe of C57BL/6 mouse with a piece of B16 melanoma tumor embedded successfully in the lobe. Clear border between host liver tissues and the embedded tumor piece was observed 14 days after embedding. No division image was noted in cells of the embedded tumor piece. In all regions surrounding the embedded tumor piece, there were few accumulations of leucocytes, lymphocytes, or giant cells, indicating a strong likelihood of immune reaction or antigen-antibody reaction, although there was active formation of fibroblast bunds and production of lysosomal enzymes. Secondary proliferous melanoic tumors developed in the environment of liver tissue separately from the embedded tumor location. Results of 14C-thymidine-nuclear labeling of embedded tumor cells showed that the majority of the labeled cells did not migrate or divide. In the case of 14C-thymidine-labeling of host liver tissue cells, results indicated no transfer of 14C-radioactivity into nuclei of embedded tumor cells, although there was positive distribution of 14C-radioactivity into nuclei of proliferous cells in the secondary tumor, a newly developed melanoic cell group. When prelabeling was performed the average density of autoradiographic image over the secondary tumor was equivalent to that over the normal liver tissue at the early stage such as 7 days after embedding and decreased with time after that. The newly developed melanoic cells were particularly exciting and proliferous, because they received much more labeling of 14C-thymidine as compared to liver tissue cells that was provided by one shot labeling of the radioactive tracer 1 h. before sacrifice of tumor embedded mice. There was no development of secondary melanoic cells in the liver lobe in case of embedding of a tumor piece previously by wrapping with a membranefilter, less 5 microns in pore size.

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Year:  1988        PMID: 3243324     DOI: 10.1007/BF03190092

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  17 in total

1.  Mechanisms of cell interaction during primary embryonic induction studied in transfilter experiments.

Authors:  S Toivonen; J Wartiovaara
Journal:  Differentiation       Date:  1976-06-04       Impact factor: 3.880

2.  Invasion of liver tissue by blood-borne mammary carcinoma cells.

Authors:  K P Dingemans
Journal:  J Natl Cancer Inst       Date:  1974-12       Impact factor: 13.506

3.  Selection of successive tumour lines for metastasis.

Authors:  I J Fidler
Journal:  Nat New Biol       Date:  1973-04-04

4.  The invasive growth of malignant tumours as a purely mechanical process.

Authors:  G Eaves
Journal:  J Pathol       Date:  1973-03       Impact factor: 7.996

5.  Cell locomation and tumor penetration. Report on a workshop of the EORTC cell surface project group.

Authors:  P Sträuli; L Weiss
Journal:  Eur J Cancer       Date:  1977-01       Impact factor: 9.162

6.  Experimental tumor cell emboli in lymph nodes.

Authors:  J Ludwig; J L Titus
Journal:  Arch Pathol       Date:  1967-09

7.  Organ selectivity for implantation survival and growth of B16 melanoma variant tumor lines.

Authors:  I J Fidler; G L Nicolson
Journal:  J Natl Cancer Inst       Date:  1976-11       Impact factor: 13.506

8.  Invasion of lymphosarcoma cells into the perfused mouse liver.

Authors:  E Roos; K P Dingemans; I V van de Pavert; M van den Bergh-Weerman
Journal:  J Natl Cancer Inst       Date:  1977-02       Impact factor: 13.506

9.  Ultrastructural study of liver sinusoids of mice during invasion by leukemic myelocytes.

Authors:  F R Campbell
Journal:  J Natl Cancer Inst       Date:  1977-02       Impact factor: 13.506

10.  An enzymatic function associated with transformation of fibroblasts by oncogenic viruses. II. Mammalian fibroblast cultures transformed by DNA and RNA tumor viruses.

Authors:  L Ossowski; J C Unkeless; A Tobia; J P Quigley; D B Rifkin; E Reich
Journal:  J Exp Med       Date:  1973-01-01       Impact factor: 14.307

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  3 in total

1.  [2-14C]Thymidine incorporation activity of stem cells in either tumor or cradle tissues in a normal or transplanted animals.

Authors:  Akiyo Shigematsu; Joji Yui; Yuko Hamai; Akiko Hatori
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2005 Jan-Jun       Impact factor: 2.441

2.  Effective local control of prostate cancer by intratumoral injection of (166)Ho-chitosan complex (DW-166HC) in rats.

Authors:  Cheol Kwak; Sung Kyu Hong; Seung Kyoo Seong; Jei Man Ryu; Moon Soo Park; Sang Eun Lee
Journal:  Eur J Nucl Med Mol Imaging       Date:  2005-08-31       Impact factor: 9.236

3.  Biodistribution and excretion of radioactivity after the administration of 166Ho-chitosan complex (DW-166HC) into the prostate of rat.

Authors:  Seung Kyoo Seong; Jei Man Ryu; Dong Hyuk Shin; Eun Jeong Bae; Akiyo Shigematsu; Yasuhiko Hatori; Junko Nishigaki; Cheol Kwak; Sang Eun Lee; Kyong Bae Park
Journal:  Eur J Nucl Med Mol Imaging       Date:  2005-04-20       Impact factor: 9.236

  3 in total

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