Thromb Haemost 2011; 106(04): 624-635
DOI: 10.1160/TH11-03-0178
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Anti-thrombotic effects of selective estrogen receptor modulator tamoxifen

Manasa K. Nayak
1   Department of Biochemistry, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
,
Sunil K. Singh
1   Department of Biochemistry, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
,
Arnab Roy
1   Department of Biochemistry, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
,
Vivek Prakash
2   Department of General Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
,
Anand Kumar
2   Department of General Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
,
Debabrata Dash
1   Department of Biochemistry, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received: 15. März 2011

Accepted after major revision: 26. Juni 2011

Publikationsdatum:
29. November 2017 (online)

Preview

Summary

Tamoxifen is a known anti-cancer drug and established estrogen receptor modulator. Few clinical studies have earlier implicated the drug in thrombotic complications attributable to lower anti-thrombin and protein S levels in plasma. However, action of tamoxifen on platelet signalling machinery has not been elucidated in detail. In the present report we show that tamoxifen is endowed with significant inhibitory property against human platelet aggregation. From a series of in vivo and in vitro studies tamoxifen was found to inhibit almost all platelet functions, prolong tail bleeding time in mouse and profoundly prevent thrombus formation at injured arterial wall in mice, as well as on collagen matrix perfused with platelet-rich plasma under arterial shear against the vehicle dimethylsulfoxide (DMSO). These findings strongly suggest that tamoxifen significantly downregulates platelet responses and holds potential as a promising anti-platelet / anti-thrombotic agent.