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PMID: 6937243 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Effects of retinoids on induction of differentiation of cultured mouse myeloid leukemia cells.

Cancer research ·Vol. 40 ·No. 3 ·1980-03-00 ·Pages 914-9

Takenaga K, Hozumi M, Sakagami Y

Abstract

Retinoic acid, retinol, retinyl acetate, and retinal induced activities of lysosomal enzymes, such as lysozyme, acid protease, and acid phosphatase, in mouse myeloid leukemia cells (M1), while the pyridyl analog of retinoic acid had no effect. Retinoic acid was the most potent inducer of lysosomal enzyme activities. The induction of lysozyme activity by retinoic acid was inhibited by treatment with puromycin. The retinoids did not induce phagocytic and locomotive activities or morphological changes in M1 cells, and they inhibited the induction of these differentiation-associated properties by various inducers without inhibiting cell growth. Retinoic acid was the most potent inhibitor of induction of these differentiation-associated properties. The inhibitory effect of retinoic acid was found to be reversible. These results suggest that distinct mechanisms exist for control of induction of lysosomal enzyme activities and of other differentiation-associated properties of M1 cells, such as phagocytosis, morphological changes, and migration.

MeSH Terms
Animals Cell Differentiation/drug effects Cell Line Cell Movement/drug effects Dexamethasone/pharmacology Diterpenes Leukemia, Experimental/enzymology,pathology Leukemia, Myeloid/pathology Lysosomes/enzymology Mice Phagocytosis/drug effects Retinaldehyde/pharmacology Retinyl Esters Tretinoin/pharmacology Vitamin A/analogs & derivatives,pharmacology
Chemicals
Diterpenes Retinyl Esters Vitamin A retinol acetate Tretinoin Dexamethasone Retinaldehyde
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Takenaga K
Hozumi M
Sakagami Y
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1980-03-00
Pages
914-9
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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