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Expression of HOXB7 in the Lung of Patients with Idiopathic Pulmonary Fibrosis: A Proof-of-Concept Study.

Authors :
Samarelli, Anna Valeria
Tonelli, Roberto
Raineri, Giulia
Mastrolia, Ilenia
Costantini, Matteo
Fabbiani, Luca
Catani, Virginia
Petrachi, Tiziana
Bruzzi, Giulia
Andrisani, Dario
Gozzi, Filippo
Marchioni, Alessandro
Masciale, Valentina
Aramini, Beatrice
Ruggieri, Valentina
Grisendi, Giulia
Dominici, Massimo
Cerri, Stefania
Clini, Enrico
Source :
Biomedicines; Jun2024, Vol. 12 Issue 6, p1321, 13p
Publication Year :
2024

Abstract

Background: The molecular pathways involved in the onset and progression of idiopathic pulmonary fibrosis (IPF) still need to be fully clarified as some are shared with lung cancer development. HOXB7, a member of the homeobox (Hox) gene family, has been found involved in various cancers. Methods: Immunohistochemical (IHC) analysis was run on lung tissue samples from surgical lung biopsy (SLB) of 19 patients with IPF, retrospectively selected from the IPF database of the University Hospital of Modena. HOXB7 expression was analyzed and compared with that of five patients with no evidence of pulmonary fibrosis as controls. Results: The semi-quantitative analysis of IHC showed that HOXB7 protein expression was higher in IPF patients compared to controls (difference between means = 6.2 ± 2.37, p = 0.0157). Further, HOXB7 expression was higher in IPF patients with a higher extent of fibrosis (50–75%)—measured with high-resolution computer tomography—compared to those with a lower extent (0–25%) (difference between means = 25.74 ± 6.72, p = 0.004). Conclusions: The expression of HOXB7 is higher in the lung of IPF patients compared to controls, and was represented in different cellular compartments within the lung niche. Further investigations are needed to clarify its role in the pathogenesis and progression of IPF. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22279059
Volume :
12
Issue :
6
Database :
Complementary Index
Journal :
Biomedicines
Publication Type :
Academic Journal
Accession number :
178160955
Full Text :
https://doi.org/10.3390/biomedicines12061321