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PMID: 2510929 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Polyamine oxidation, programmed cell death, and regulation of melanoma in the murine embryonic limb.

Cancer research ·Vol. 49 ·No. 23 ·1989-12-01 ·Pages 6680-6

Parchment RE, Pierce GB

Abstract

The murine embryonic limb at day 14 of gestation suppresses tumor formation by melanoma cells. Conditioned media of embryonic limbs have been found cytotoxic for B16 melanoma cells. The cytotoxicity is due to the catabolism of polyamines in the limb bud extracts by an amine oxidase in the serum supplement of the culture medium. However, a polyamine oxidase activity, similar to that in adult rat liver, is also detectable in homogenates of embryonic limbs. Thus, the embryonic limb contains the necessary components to produce polyamine-derived cytotoxic metabolites, which are present at the time programmed cell death occurs. This leads to the hypothesis that injected melanoma cells are killed incidentally by the mechanism that mediates programmed cell death.

MeSH Terms
Amine Oxidase (Copper-Containing)/metabolism Animals Cell Survival Cytotoxins/physiology Extremities/embryology Melanoma, Experimental/pathology Mice Organ Culture Techniques Oxidoreductases Acting on CH-NH Group Donors/metabolism Polyamines/metabolism Transforming Growth Factors/physiology Tumor Cells, Cultured
Chemicals
Cytotoxins Polyamines Transforming Growth Factors Amine Oxidase (Copper-Containing) Oxidoreductases Acting on CH-NH Group Donors polyamine oxidase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Parchment R E
Department of Pathology, University of Colorado School of Medicine, Denver 80262.
Pierce G B
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1989-12-01
Pages
6680-6
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · CA 35367 · United States
NCI NIH HHS · CA-47369 · United States
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