Intracrine PTHrP protects against serum starvationinduced apoptosis and regulates the cell cycle in MCF-7 breast cancer cells

Veronica A. Tovar Sepulveda, Xiaoli Shen, Miriam Falzon

Research output: Contribution to journalArticle

79 Scopus citations

Abstract

PTHrP is secreted by breast cancer cells in vivo and in vitro. In the breast cancer cell line MCF-7, PTHrP overexpression is associated with increased mitogenesis. We used this cell line to study the mechanism for the proliferative effects of PTHrP. Clonal MCF-7 lines were established overexpressing wildtype PTHrP or PTHrP mutated in the nuclear localization signal (NLS). Mutation of the NLS negated the proliferative effects and nuclear trafficking of PTHrP, indicating that increased mitogenesis is mediated via an intracrine pathway. Cells overexpressing wild-type PTHrP were enriched in G2 + M stage of the cell cycle compared with cells overexpressing NLS-mutated PTHrP, indicating an intracrine role for PTHrP in cell cycle regulation. Wild-type PTHrP also protected MCF-7 cells from serum starvation.induced apoptosis. Cells overexpressing wild-type PTHrP showed significantly greater cell survival than cells overexpressing NLS-mutated PTHrP. The ratios of the apoptosis-regulating proteins Bc1-2 to Bax and Bc1-xL to Bax were higher in cells overexpressing wild-type, but not NLS-mutated, PTHrP compared with control cells. These findings suggest that the proliferative effects of PTHrP in breast cancer cells are mediated through regulation of the cell cycle and apoptosis, and that controlling PTHrP production in breast cancer may be therapeutically useful.

Original languageEnglish (US)
Pages (from-to)596-606
Number of pages11
JournalEndocrinology
Volume143
Issue number2
DOIs
StatePublished - Jan 1 2002

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ASJC Scopus subject areas

  • Endocrinology

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