Thromboxane A2 modulates cisplatin-induced apoptosis through a Siva1-dependent mechanism.

Cell Death and Differentiation
C Iorio-MorinJ-L Parent

Abstract

Thromboxane A(2) (TXA(2)) is an important lipid mediator whose function in apoptosis is the subject of conflicting reports. Here, a yeast two-hybrid screen for proteins that interact with the C-terminus of the TXA(2) receptor (TP) identified Siva1 as a new TP-interacting protein. Contradictory evidence suggests pro- and anti-apoptotic roles for Siva1. We show that a cisplatin treatment induces TXA(2) synthesis in HeLa cells. We demonstrate that endogenous TP stimulation promotes cisplatin-induced apoptosis of HeLa cells and that such modulation requires the expression of Siva1, as evidenced by inhibiting its endogenous expression using siRNAs. We reveal that, upon stimulation of TP, degradation of Siva1 is impeded, resulting in an accumulation of the protein, which translocates from the nucleus to the cytosol. Translocation of Siva1 correlates with its reduced interaction with Mdm2 (an inhibitor of p53 signalling), as well as with its increased interaction with TRAF2 and XIAP (known to enhance pro-apoptotic signalling). Our data provide a model that reconciles the pro- and anti-apoptotic roles that were reported for Siva1 and identify a new mechanism for promoting apoptosis by G protein-coupled receptors. Our findings may have ...Continue Reading

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Citations

Jun 25, 2014·The Journal of Cell Biology·Jinhua HanJun Huang
Nov 7, 2014·Asian Pacific Journal of Cancer Prevention : APJCP·Ya-Han ZhangXia Yu
Jun 5, 2015·Acta Biochimica Et Biophysica Sinica·Guang-Zhe GeCeshi Chen
Jul 11, 2020·Cell Biochemistry and Biophysics·Xiao-Tong WangWei Mai
Mar 26, 2021·Cell Reports Medicine·Polina MamoshinaAlfonso Bueno-Orovio

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