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1.
Genes Cells ; 21(3): 226-40, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26891792

ABSTRACT

Doxorubicin is a widely used chemotherapeutic agent, but its utility is limited by cellular resistance and off-target effects. To understand the molecular mechanisms regulating chemotherapeutic responses to doxorubicin, we previously carried out a genomewide search of doxorubicin-resistance genes in Schizosaccharomyces pombe fission yeast and showed that these genes are organized into networks that counteract doxorubicin cytotoxicity. Here, we describe the identification of a subgroup of doxorubicin-resistance genes that, when disrupted, leads to reduced tolerance to exogenous calcium. Unexpectedly, we observed a suppressive effect of calcium on doxorubicin cytotoxicity, where concurrent calcium and doxorubicin treatment resulted in significantly higher cell survival compared with cells treated with doxorubicin alone. Conversely, inhibitors of voltage-gated calcium channels enhanced doxorubicin cytotoxicity in the mutants. Consistent with these observations in fission yeast, calcium also suppressed doxorubicin cytotoxicity in human breast cancer cells. Further epistasis analyses in yeast showed that this suppression of doxorubicin toxicity by calcium was synergistically dependent on Rav1 and Vph2, two regulators of vacuolar-ATPase assembly; this suggests potential modulation of the calcium-doxorubicin interaction by fluctuating proton concentrations within the cellular environment. Thus, the modulatory effects of drugs or diet on calcium concentrations should be considered in doxorubicin treatment regimes.


Subject(s)
Calcium/pharmacology , Doxorubicin/toxicity , Topoisomerase II Inhibitors/toxicity , Calcium Channel Blockers/pharmacology , Cell Survival , Drug Resistance, Fungal/genetics , Genes, Fungal , Humans , MCF-7 Cells , Schizosaccharomyces/drug effects , Schizosaccharomyces/metabolism
2.
Appetite ; 58(2): 754-7, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22178007

ABSTRACT

The present study demonstrates the utility of a social identity analysis of social influence in predicting eating behavior. In a laboratory experiment, female undergraduate students observed a confederate who appeared to have eaten a large or small amount of popcorn. The confederate was presented as either a fellow in-group member of a salient identity (same university) or an out-group member (another tertiary institution). Results supported the hypothesis that modeling of eating behavior only occurs for psychologically salient in-group members; there was no modeling of out-group members' eating. These data also provide clear evidence of a psychological mechanism by which the modeling of eating behavior can occur.


Subject(s)
Feeding Behavior/psychology , Social Identification , Female , Food Preferences/psychology , Humans , Social Behavior , Students/psychology , Surveys and Questionnaires , Young Adult
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