| Literature DB >> 32748739 |
Panagiotis Paliogiannis1, Sara Solveig Fois1, Alessandro Giuseppe Fois1, Antonio Cossu1, Giuseppe Palmieri2, Gianfranco Pintus3.
Abstract
Idiopathic pulmonary fibrosis (IPF) is an aggressive pulmonary disease which shares several molecular, pathophysiological and clinical aspects with lung cancer, including high mortality rates. The antifibrotic drugs Nintedanib and Pirfenidone have recently been introduced in clinical practice for the treatment of IPF. Nintedanib is also used for the treatment of several malignancies, including non-small cell lung cancer (NSCLC) in combination with Docetaxel, while Pirfenidone showed some anti-neoplastic effects in preclinical studies. On the other hand, novel targeted agents and immunotherapies have been introduced in the last decade for the treatment of NSCLC, and some of them showed anti-fibrotic properties in recent studies. These evidences, based on the common pathophysiological backgrounds of IPF and lung cancer, make possible the mutual or combined use of anti-fibrotic and anti-neoplastic drugs to treat these highly lethal diseases. The aim of the present review is to depict the current scientific landscape regarding the repurposing of anti-neoplastic drugs in IPF and anti-fibrotic drugs in lung cancer, and to identify future research perspectives on the topic. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: Idiopathic pulmonary fibrosis; anticancer drugs; antifibrotic drug; cancer; drugzzm321990repurposing; fibrosis; lung cancer; nintedanib; pirfenidone
Year: 2021 PMID: 32748739 DOI: 10.2174/0929867327999200730173748
Source DB: PubMed Journal: Curr Med Chem ISSN: 0929-8673 Impact factor: 4.530