Histone methylation status of H3K4me3 and H3K9me3 under methionine restriction is unstable in methionine-addicted cancer cells, but stable in normal cells-Reference-Cited by-同舟云学术

Histone methylation status of H3K4me3 and H3K9me3 under methionine restriction is unstable in methionine-addicted cancer cells, but stable in normal cells

Published:2020-12 Issue:4 Volume:533 Page:1034-1038
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Yamamoto Jun,Han Qinghong,Inubushi Sachiko^ORCID,Sugisawa Norihiko^ORCID,Hamada Kazuyuki,Nishino Hiroto,Miyake Kentaro,Kumamoto Takafumi,Matsuyama Ryusei,Bouvet Michael,Endo Itaru^ORCID,Hoffman Robert M.

Funder

Yokohama City University

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference27 articles.

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2. Reduced availability of endogenously synthesized methionine for S-adenosylmethionine formation in methionine-dependent cancer cells;Coalson;Proc. Natl. Acad. Sci. Unit. States Am.,1982

3. Reduced free-methionine in methionine-dependent SV40-transformed human fibroblasts synthesizing apparently normal amounts of methionine;Stern;J. Cell. Physiol.,1983

4. Elevated overall rates of transmethylation in cell lines from diverse human tumors;Stern;In Vitro,1984

5. Altered methionine metabolism occurs in all members of a set of diverse human tumor cell lines;Stern;J. Cell. Physiol.,1984

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