Skip to main navigation Skip to search Skip to main content

Linkage of methionine dependence and other features of malignancy

  • AntiCancer, Inc.
  • University of California at San Diego

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

1 Scopus citations

Abstract

Cancer cells have an elevated methionine (MET) requirement compared to normal cells and are termed MET dependent. Cancer cells were isolated in MET-restricted (MR) medium that reverted from MET dependence to MET independence. Increased MET biosynthesis was not a prerequisite for reversion to MET independence, indicating that MET dependence was not due to reduced endogenous MET synthesis. MET-independent revertants of cancer cells concomitantly reverted for some of the other properties associated with malignancy: Of the 13 MET-independent revertants isolated 5 showed increased anchorage dependence as reflected by reduced cloning efficiencies in methylcellulose; 8 showed an increased serum requirement for optimal growth; 8 showed decreased cell density in medium containing high serum; and 3 altered their cell morphology significantly. Eight of the 13 revertants have increased chromosome numbers. Thus, by selecting for MET independence, it is possible to obtain heterogeneous reduced-malignancy revertants, indicating further a relationship between altered MET metabolism and other fundamental properties of oncogenic transformation.

Original languageEnglish
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages27-36
Number of pages10
DOIs
StatePublished - 2019

Publication series

NameMethods in Molecular Biology
Volume1866
ISSN (Print)1064-3745

Keywords

  • Anchorage dependence
  • Cancer cells
  • Cell morphology
  • Chromosomes
  • Methionine dependence
  • Methionine independence
  • Methionine synthase
  • Revertants
  • Serum dependence
  • Transmethylation

Fingerprint

Dive into the research topics of 'Linkage of methionine dependence and other features of malignancy'. Together they form a unique fingerprint.

Cite this