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Mitochondrial dysfunction is a key determinant of the rare disease lymphangioleiomyomatosis and provides a novel therapeutic target

Abdelwahab, Elhusseiny Mahmoud Mohamed and Pal, Szilard and Kvell, Krisztian and Sarosi, Vera and Bai, Peter and Rue, R. and Krymskaya, V. and McPhail, D. and Porter, A. and Pongracz, Judit (2019) Mitochondrial dysfunction is a key determinant of the rare disease lymphangioleiomyomatosis and provides a novel therapeutic target. ONCOGENE, 38 (16). pp. 3093-3101. ISSN 0950-9232

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Abstract

Lymphangioleiomyomatosis (LAM) is a rare and progressive systemic disease affecting mainly young women of childbearing age. A deterioration in lung function is driven by neoplastic growth of atypical smooth muscle-like LAM cells in the pulmonary interstitial space that leads to cystic lung destruction and spontaneous pneumothoraces. Therapeutic options for preventing disease progression are limited and often end with lung transplantation temporarily delaying an inevitable decline. To identify new therapeutic strategies for this crippling orphan disease, we have performed array based and metabolic molecular analysis on patient-derived cell lines. Our results point to the conclusion that mitochondrial biogenesis and mitochondrial dysfunction in LAM cells provide a novel target for treatment.

Item Type: Article
Subjects: R Medicine / orvostudomány > RM Therapeutics. Pharmacology / terápia, gyógyszertan
Depositing User: dr Krisztian Kvell
Date Deposited: 13 Sep 2019 14:49
Last Modified: 13 Sep 2019 14:49
URI: http://real.mtak.hu/id/eprint/99306

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