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World J Clin Cases. Nov 16, 2014; 2(11): 668-675
Published online Nov 16, 2014. doi: 10.12998/wjcc.v2.i11.668
Promising new treatment targets in patients with fibrosing lung disorders
Martina Sterclova, Martina Vasakova
Martina Sterclova, Martina Vasakova, Department of Respiratory Medicine, Thomayer Hospital and 1st Medical Faculty of Charles University, Prague 14000, Czech Republic
Author contributions: Sterclova M wrote the paper; Vasakova M critically revised the paper.
Supported by IGA Grant G 1207 (Internal Grant Agency of the Czech Ministry of Health)
Correspondence to: Martina Sterclova, MD, PhD, Department of Respiratory Medicine, Thomayer Hospital and 1st Medical Faculty of Charles University, Videnska 800, Prague 14000, Czech Republic. martinasafrankova@seznam.cz
Telephone: +420-261-082163 Fax: +420-261-082206
Received: May 20, 2014
Revised: July 21, 2014
Accepted: September 6, 2014
Published online: November 16, 2014
Processing time: 173 Days and 14.5 Hours
Abstract

The processes of lung fibrogenesis and fibrotic healing are common to a number of conditions with different etiologies. The lungs are the only affected organ in some cases, whereas in others, several organ systems are involved. Therapeutic options can be discussed from various perspectives. In this review, we address the localization of therapeutic targets with regard to cell compartments, including secreted ligands, cell surface, plasma membrane-cytosol interplay, cytosol and nucleus. Complex approach using stem cell therapy is also discussed. As the prognosis of patients with these disorders remains grim, treatment combinations targeting different molecules within the cell should sometimes be considered. It is reasonable to assume that blocking specific pathways will more likely lead to disease stabilization, while stem cell-based treatments could potentially restore lung architecture. Gene therapy could be a candidate for preventive care in families with proven specific gene polymorphisms and documented familial lung fibrosis. Chronobiology, that takes into account effect of circadian rhythm on cell biology, has demonstrated that timed drug administration can improve treatment outcomes. However, the specific recommendations for optimal approaches are still under debate. A multifaceted approach to interstitial lung disorders, including cooperation between those doing basic research and clinical doctors as well as tailoring research and treatment strategies toward (until now) unmet medical needs, could improve our understanding of the diseases and, above all, provide benefits for our patients.

Keywords: Interstitial lung disease; Treatment; Idiopathic pulmonary fibrosis; Connective tissue disease; Cell compartments; Signaling molecules; Signal transducers; Transcription factors

Core tip: Novel treatment targets in patients with fibrosing interstitial lung diseases are summarized. Targets are listed according to defined cell compartments. Ongoing clinical studies focusing on some of the promising targets provide insight into current progress in lung fibrosis research.