Publish in this journal
Journal Information
Vol. 54. Num. 1.January 2018
Pages 1-58
Vol. 54. Num. 1.January 2018
Pages 1-58
DOI: 10.1016/j.arbr.2017.07.015
Telomere Shortening in Idiopathic Pulmonary Fibrosis
Acortamiento de los telómeros en fibrosis pulmonar idiopática
María Molina-Molinaa,b,
Corresponding author

Corresponding author.
, Lurdes Planas-Cerezalesa,b, Rosario Peronac,d
a Unidad Funcional de Intersticio Pulmonar (UFIP), Servicio de Neumología, Hospital Universitario de Bellvitge, IDIBELL, L’Hospitalet de Llobregat, Barcelona, Spain
b Centro de Investigación en Red de Enfermedades Respiratorias (CIBERES), Spain
c Instituto de Investigaciones Biomédicas «Alberto Sols», CSIC-UAM, Madrid, Spain
d Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Spain
This item has received
Article information
Full Text
Download PDF
Full Text

We are currently experiencing the rapid translation of a recent investigational advance into clinical practice: telomere testing and its implications in patients with pulmonary fibrosis. Idiopathic pulmonary fibrosis (IPF) is the most prevalent fibrosing interstitial disease (13–20/100000 inhabitants) and the one with the worst prognosis.1,2 The disease is defined as familial pulmonary fibrosis (FPF) when it occurs in 2 or more individuals from the same family,1 and it is in this setting that the first studies have pointed to telomere alterations as a risk factor for pulmonary fibrosis.3

At the beginning of the 21st century, Selman et al. reported that the pathogenesis of pulmonary fibrosis was based on changes in tissue repair after alveolar damage; several profibrotic pathways and mediators prevent reepithelialization, perpetuating the damage and culminating in the invasion of the alveolar space by a proliferative matrix tissue that lacks respiratory functionality.4,5 The regulation of some of these profibrotic mediators led to the first antifibrotic treatments capable of slowing disease progression.2 However, we are as yet unable to stop this fatal degenerative progress, nor can the lung recover its reparative capacity to improve or cure the disease.2,5 An understanding of why the tissue does not repair itself is essential if we are to prevent the perpetuation of the process. Recent studies in this area have pointed to accelerated aging and cellular reprogramming abnormalities as a source or cause of the reparative changes.6 It is common knowledge that newborns regenerate, repair and restore damaged tissues to their original functional status, and that this ability reduces physiologically with age, to the point that a simple fracture in an elderly person is frequently associated with functional loss and even fatal complications. One of the mechanisms closely related with the physiological process of aging is progressive telomere shortening.6 In diseases typically associated with accelerated aging and genetic instability due to premature telomere shortening, such as congenital dyskeratosis, pulmonary fibrosis develops spontaneously after the first decade of life.7

Telomeres are repeated sequences in the DNA and associated proteins (the shelterin complex) that are critical for the protection and stability of the internal sequences of the chromosomes: this function is called “capping”.6,7 Telomeres shorten in each cell division. Telomerase is a reverse transcriptase that carries its own RNA component and promotes correct chromosome end replication.7 However, most human cells lack sufficient telomerase activity to maintain telomere size indefinitely, and the telomeres gradually shorten. When the telomeres shorten to a critical size, the cell cycle enters into permanent shutdown (senescence) or apoptosis.7,8 Accelerated telomere shortening is associated with premature aging, abnormal tissue repair, and the resulting pathogenic consequences.6,7 This dysfunction may be congenital due to genetic mutations, or acquired by epigenetic alterations, such as telomere methylation. In adult tissue, telomerase activity aimed at repairing tissue damage is expressed in germ cells and in stem cells.8 In the last 10 years, the role of telomere size in the acquisition of pluripotency and somatic cell reprogramming has been underlined. This phenomenon would be of significance both in tissue embryogenesis, and later, in the reparative processes of cells and tissues.6–10

In IPF and FPF, mutations have been described in genes of the telomere protein complex, telomere subunits or regulatory proteins (TERT, TERC, DKC1, PARN, RTEL1, TINF1, OBFC1, NAF1) that contribute to telomere shortening and cell senescence by reducing telomere activity.8–12 Exhaustion and decline of stem cells, both in the bronchial and alveolar epithelial stem cell niches, have been proposed as a contributing factor in altered regenerative capacity.6–8 Telomere shortening is described in 25% of IPF patients and in over 50% of FPF patients, and contributes to increased epithelial apoptosis.11 Patients with telomere shortening, particularly those with FPF, have a worse prognosis and more morbidity after transplantation.9,10 It has recently been observed that the existence of telomere shortening is a factor for poor progress, irrespective of the radiological and histological pattern of the FPF.9 However, the effect of telomere shortening on the development of the disease is still debated, and it has been indicated that telomere shortening is more of a catalyst than a direct cause of pulmonary fibrosis.12 Le Saux et al. found that the induction of pulmonary fibrosis is greater in the presence of a TERT mutation, and that this effect could be inhibited in an animal model by inducing telomerase activity.12 Gestelmir (GSE24-2), a dyskerin internal peptide containing 55 amino acids, induces telomerase activity, restores telomere length, and decreases aging in cells with telomere shortening in dyskeratosis.13 Transfection of cells with GSE24.2 not only increases levels of hTERT RNA and hTR, but also modifies the metabolism of different anti-inflammatory and antifibrotic mediators.13 Preliminary results show that gestelmir transfection of commercial fibrotic lung cell lines, modified by telomeric silencing, recovers telomerase activity and reduces oxidative stress.13 In addition to these promising preclinical data, danazol, an androgenic analog, has been shown to inhibit telomere shortening in patients with different diseases associated with this alteration.14 However, the data in pulmonary fibrosis are not conclusive, so it cannot be recommended for use until specifically designed studied have been conducted.

The study of telomere shortening in IPF, then, contributes not only predictive data on progress (biomarker), but also anticipates possible complications associated with transplantation, and represents a future therapeutic target for a subset of patients (precision medicine). For this reason, it provides useful non-invasive clinical information in many cases, primarily young IPF and FPG patients. However, this new knowledge is generating more questions than answers: Why do not all individuals with telomere shortening develop the disease? What determines the variability of the prognosis? What lung biology is associated with telomere shortening? What are the implications of having long telomeres? How does patient management vary? What about family members? Answering these and other questions with new research studies and international consensus will be of particular importance for the future clinical application of these advances in IPF and other fibrosing lung diseases.15


PI15/00710 and PI14/01595ISCIII-FEDER Funds.

Conflict of Interests

Maria Molina-Molina has received grants from Boeringher Ing., Roche, Intermune, Glaxo SMK, Chiesi, Astra-Zeneca, Esteve, and BRN. The other authors have no conflict of interests.

G. Raghu,H.L. Collard,J.J. Egan,F.J. Martinez,J. Behr,K.K. Brown
An official ATS/ERS/JRS/ALAT statement: IPF: evidence-based guidelines for diagnosis and management
Am J Respir Crit Care Med, 183 (2011), pp. 788-824
A. Xaubet,M. Molina-Molina,O. Acosta,E. Bollo,D. Castillo,E. Fernández-Fabrellas
Guidelines for the medical treatment of idiopathic pulmonary fibrosis
Arch Bronconeumol, 53 (2017), pp. 263-269
M.Y. Armanios,J.J. Chen,J.D. Cogan,J.K. Alder,R.G. Ingersoll,C. Markin
Telomerase mutations in families with idiopathic pulmonary fibrosis
N Engl J Med, 356 (2007), pp. 1317-1326
B.D. Uhal,J.K. Kim,X. Li,M. Molina-Molina
Angiotensin-TGF-1 crosstalk in IPF: autocrine mechanisms in myofibroblasts and macrophages
Curr Pharm Des, 13 (2007), pp. 1247-1346
T.E. King Jr.,A. Pardo,M. Selman
Idiopathic pulmonary fibrosis
M. Selman,A. Pardo
Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. An integral model
Am J Resp Crit Care Med, 189 (2014), pp. 1161-1172
M. Armanios
Telomeres and age-related diseases: how telomere biology informs clinical paradigms
J Clin Invest, 123 (2013), pp. 996-1002
C.M. Kong,X.W. Lee,W.X. Ang
Telomere shortening in human diseases
FEBS J, 280 (2013), pp. 3180-3193
C.A. Newton,K. Batra,J. Torrealba,J. Kozlitina,C.S. Glazer,C. Aravena
Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive
Eur Respir J, 48 (2016), pp. 1710-1720
B.D. Stuart,J.S. Lee,J. Kozlitina,I. Noth,M.S. Devine,C.S. Glazer
Effect of telomere length on survival in patients with idiopathic pulmonary fibrosis: an observational cohort study with independent validation
Lancet Respir Med, 2 (2014), pp. 557-565
S. Meiners,O. Eickelberg,M. Königshoff
Hallmarks of the ageing lung
Eur Respir J, 45 (2015), pp. 807-827
C.J. Le Saux,P. Davy,C. Brampton,S.S. Ahuja,S. Fauce,P. Shivshankar
A novel telomerase activator suppresses lung damage in a murine model of idiopathic pulmonary fibrosis
C. Manguan-Garcia,L. Pintado-Berniches,J. Carrillo,R. Machado-Pinilla,L. Sastre,C. Pérez-Quilis
Expression of the genetic suppressor element 24.2 (GSE24.2) decreases DNA damage and oxidative stress in X-linked dyskeratosis congenital cells
D.M. Townsley,B. Dumitriu,D. Liu,A. Biancotto,B. Weinstein,C. Chen
Danazol treatment for telomere diseases
N Engl J Med, 374 (2016), pp. 1922-1931
R. Borie,C. Kannengiesser,M.P. Debray,B. Crestani
The genetic diagnosis of interstitial lung disease: a need for an international consensus
Am J Respir Crit Care Med, 195 (2017), pp. 1538-1539

Please cite this article as: Molina-Molina M, Planas-Cerezales L, Perona R. Acortamiento de los telómeros en fibrosis pulmonar idiopática. Arch Bronconeumol. 2018;54:3–4.

Copyright © 2017. SEPAR
Archivos de Bronconeumología (English Edition)

Subscribe to our Newsletter

Article options
Cookies policy
To improve our services and products, we use cookies (own or third parties authorized) to show advertising related to client preferences through the analyses of navigation customer behavior. Continuing navigation will be considered as acceptance of this use. You can change the settings or obtain more information by clicking here.