Volume 19, Issue 2 pp. 290-292
SCIENTIFIC LETTER

Mammalian target of rapamycin (mTOR) inhibition does not prevent lung adenocarcinoma-induced malignant pleural effusion

Maria-Eleni Vazakidou

Maria-Eleni Vazakidou

1st Department of Critical Care and Pulmonary Services, School of Medicine, Evangelismos Hospital, University of Athens, Athens, Greece

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Sofia Magkouta

Sofia Magkouta

1st Department of Critical Care and Pulmonary Services, School of Medicine, Evangelismos Hospital, University of Athens, Athens, Greece

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Charalambos Moschos

Charalambos Moschos

1st Department of Critical Care and Pulmonary Services, School of Medicine, Evangelismos Hospital, University of Athens, Athens, Greece

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Ioannis Kalomenidis

Corresponding Author

Ioannis Kalomenidis

1st Department of Critical Care and Pulmonary Services, School of Medicine, Evangelismos Hospital, University of Athens, Athens, Greece

Correspondence: Ioannis Kalomenidis, ‘Marianthi Simou Lab’, 3 Ploutarchou Street, 10675, Athens, Greece. Email: [email protected]Search for more papers by this author
First published: 02 July 2013
Citations: 3

Conflict of Interest Statement

Dr Ioannis Kalomenidis, as group leader, has received research funding from Wyheth Hellas SA for this and other projects.

Abstract

The impact of temsirolimus was investigated in a murine model of malignant pleural effusion (MPE) created with intrapleural injection of Lewis Lung Cancer (LLC) cells. Temsirolimus (1 or 20 mg/kg) did not affect the pleural fluid volume or the number of pleural tumour foci. In addition, temsirolimus did not affect vascular endothelial growth factor expression by LLC cells in vitro. In conclusion, temsirolimus did not curtail experimental lung-adenocarcinoma-induced MPE.

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