M

Mary E. Anderson

University of Iowa

ORCID: 0000-0001-5342-530X

Publishes on Sulfur Compounds in Biology, Glutathione Transferases and Polymorphisms, Muscle Physiology and Disorders. 123 papers and 17.8k citations.

123Publications
17.8kTotal Citations

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Top publicationsby citations

GLUTATHIONE
Alton Meister, Mary E. Anderson|Annual Review of Biochemistry|1983
Cited by 5.6k

The Hippo pathway was initially discovered in Drosophila melanogaster as a key regulator of tissue growth. It is an evolutionarily conserved signaling cascade regulating numerous biological processes, including cell growth and fate decision, organ size ...Read More

High resistance to cisplatin in human ovarian cancer cell lines is associated with marked increase of glutathione synthesis.
Andrew K. Godwin, A Meister, P J O'Dwyer et al.|Proceedings of the National Academy of Sciences|1992
Cited by 928Open Access

Exposure of human ovarian tumor cell lines to cisplatin led to development of cell lines that exhibited increasing degrees of drug resistance, which were closely correlated with increase of the levels of cellular glutathione. Cell lines were obtained that showed 30- to 1000-fold increases in resistance; these cells also had strikingly increased (13- to 50-fold) levels of glutathione as compared with the drug-sensitive cells of origin. These levels of resistance to cisplatin and the cellular glutathione levels are substantially greater than previously reported. Very high cisplatin resistance was associated with enhanced expression of mRNAs for gamma-glutamylcysteine synthetase and gamma-glutamyl transpeptidase; immunoblots showed increase of gamma-glutamylcysteine synthetase but not of glutathione synthetase. Glutathione S-transferase activity was unaffected, as determined with chlorodinitrobenzene as a substrate. These studies suggest the potential value of examining regulation of glutathione synthesis as an indicator of clinical prognosis. The highly resistant cell lines are proving useful for studying the multiple mechanisms by which tumor cells acquire drug- and radiation-resistance.