Store-operated Ca2+ entry in rhabdomyosarcoma cells

• Published in: Biochemical and biophysical research communications 2016-08, Vol.477 (1), p.129-136
• Main Authors: Schmid, Evi, Stagno, Matias Julian, Yan, Jing, Stournaras, Christos, Lang, Florian, Fuchs, Jörg, Seitz, Guido
• Format: Article
• Language: English
• Subjects: adenosinetriphosphatase; calcium; cell death; cell movement; Cell proliferation; fluorescence; humans; ion channels; metastasis; Migration; mitosis; Orai1; radiotherapy; reverse transcriptase polymerase chain reaction; Rhabdomyosarcoma; sarcoma; SOCE; transcription factor NF-kappa B; Western blotting
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2016.06.032

Rhabdomyosarcoma (RMS), the most common pediatric soft tissue sarcoma, has an intrinsic or early-acquisition of resistance to chemo- and radiation therapy. Molecular determinants pivotal for RMS migration, metastatic invasion, cell proliferation, and survival are incompletely identified. Migration and cell proliferation were shown to correlate with cytosolic Ca2+ activity ([Ca2+]i). Store-operated Ca2+-entry (SOCE) that increases intracellular [Ca2+] is accomplished by Orai1, a pore-forming ion channel unit, the expression of which is stimulated by the transcription factor NFκB. The present study explored the expression of Orai1 and its regulators STIM1 and NFκB in human rhabdomyosarcoma cell lines and analyzed their impact on cell proliferation and migration. For the study human rhabdomyosarcoma cell lines RD (embryonal) and RH30 (alveolar) were analyzed for Orai1, STIM1, and NFκB transcription by RT-PCR and their corresponding proteins in Western blot. [Ca2+]i was detected via Fura-2 fluorescence and SOCE – resulting from [Ca2+]i increase following store depletion with extracellular Ca2+ removal and inhibition of the sarcoendoplasmatic reticular Ca2+ ATPase – detected with thapsigargin. Cell migration was analyzed in transwell and mitotic cell death with the clonogenic assay. In summary, Orai1, STIM1, and NFκB are expressed in embryonal (RD) and alveolar (RH30) rhabdomyosarcoma. SOCE inhibitor BTP2, Orai1 inhibitor 2-APB, or NFκB inhibitor wogonin virtually abrogated (BTP2, 2-APB) or significantly reduced (wogonin) SOCE. Moreover, SOCE inhibitors 2-APB and BTP2 and wogonin significantly inhibited migration and proliferation of both, RD and RH30 cells. These results suggest that Orai1 signaling is involved in SOCE into rhabdomyosarcoma cells thus contributing to migration, invasion and proliferation. •Orai1, STIM1, and NFκB are expressed in RD and RH30 rhabdomyosarcoma cell lines.•Orai1, STIM1, and NFκB are significantly upregulated in the RH30 cell line and leads to a significantly increased SOCE.•Orai1 signaling is involved in SOCE thus contributing to migration, invasion and proliferation.