Abstract

Simple SummaryBreast cancer shows a high heterogeneity which accounts for cancer subtype aggressiveness. Store-operated calcium entry (SOCE) is significantly remodeled in breast cancer cells and supports a variety of cancer hallmarks. Here we show that breast cancer cells from different subtypes exhibit a variable Orai1:Orai2 expression ratio. In cells with a high Orai2 expression, Orai2 modulates the magnitude SOCE and support Ca2+ oscillations in response to agonists, thus modulating the activation of the transcription factors NFAT1 and NFAT4. Furthermore, Orai2 plays a relevant role in cell cycle progression and apoptosis resistance.Breast cancer is a heterogeneous disease from the histological and molecular expression point of view, and this heterogeneity determines cancer aggressiveness. Store-operated Ca2+ entry (SOCE), a major mechanism for Ca2+ entry in non-excitable cells, is significantly remodeled in cancer cells and plays an important role in the development and support of different cancer hallmarks. The store-operated CRAC (Ca2+ release-activated Ca2+) channels are predominantly comprised of Orai1 but the participation of Orai2 and Orai3 subunits has been reported to modulate the magnitude of Ca2+ responses. Here we provide evidence for a heterogeneous expression of Orai2 among different breast cancer cell lines. In the HER2 and triple negative breast cancer cell lines SKBR3 and BT20, respectively, where the expression of Orai2 was greater, Orai2 modulates the magnitude of SOCE and sustain Ca2+ oscillations in response to carbachol. Interestingly, in these cells Orai2 modulates the activation of NFAT1 and NFAT4 in response to high and low agonist concentrations. Finally, we have found that, in cells with high Orai2 expression, Orai2 knockdown leads to cell cycle arrest at the G0-G1 phase and decreases apoptosis resistance upon cisplatin treatment. Altogether, these findings indicate that, in breast cancer cells with a high Orai2 expression, Orai2 plays a relevant functional role in agonist-evoked Ca2+ signals, cell proliferation and apoptosis resistance.

Highlights

  • Store-operated Ca2+ entry (SOCE) is a major mechanism for Ca2+ influx in nonexcitable cells regulated by the filling state of the agonist-releasable intracellular Ca2+ stores [1]

  • Our results indicate that Orai2 is required for cell cycle progression and apoptosis resistance in cells with a high Orai2 expression

  • According to the Cancer Genome Atlas (TCGA) database and analyzed using UALCAN [26], Orai1 and Orai2 mRNA expression is significantly higher in breast cancer tissues than in normal tissues (Figure S1), and this difference was consistent across groups stratified by cancer subtypes

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Summary

Introduction

Store-operated Ca2+ entry (SOCE) is a major mechanism for Ca2+ influx in nonexcitable cells regulated by the filling state of the agonist-releasable intracellular Ca2+ stores [1]. Orai and Orai has been reported to modulate the magnitude of SOCE in a variety of cell types, including HEK293 cells [4,5], human Hs27 fibroblasts [5], the chondrocyte cell line OUMS-27 [6], Jurkat T cells [7], primary ameloblasts [8] and human neuroglioma derived cells [9], as well as in Ora2-deficient mice [5] This phenomenon is probably mediated because Orai and Orai have a greater sensitivity to Ca2+-dependent inactivation than Orai1 [10,11]. Unlike Orai, Orai and Orai share some biochemical features such as their sensitivity to pH, so that Orai and Orai currents are inhibited by acidification and enhanced by alkalization, while those of Orai are unaffected [15,16]

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