The Ferroxidase Hephaestin in Lung Cancer: Pathological Significance and Prognostic Value

Hephaestin (HEPH) belongs to a group of exocytoplasmic ferroxidases which contribute to cellular iron homeostasis by favouring its export. Down-regulation of HEPH expression, possibly by stimulating cell proliferation due to an increase in iron availability, has shown to correlate with poor survival...

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Published inFrontiers in oncology Vol. 11; p. 638856
Main Authors Zacchi, Paola, Belmonte, Beatrice, Mangogna, Alessandro, Morello, Gaia, Scola, Letizia, Martorana, Anna, Borelli, Violetta
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 19.05.2021
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ISSN2234-943X
2234-943X
DOI10.3389/fonc.2021.638856

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Summary:Hephaestin (HEPH) belongs to a group of exocytoplasmic ferroxidases which contribute to cellular iron homeostasis by favouring its export. Down-regulation of HEPH expression, possibly by stimulating cell proliferation due to an increase in iron availability, has shown to correlate with poor survival in breast cancer. The lung is particularly sensitive to iron-induced oxidative stress, given the high oxygen tension present, however, HEPH distribution in lung cancer and its influence on prognosis have not been investigated yet. In this study we explored the prognostic value of HEPH and its expression pattern in the most prevalent histotypes of lung cancers, namely lung adenocarcinoma and lung squamous cell carcinoma. In silico analyses, based on UALCAN, Gene Expression Profiling Interactive Analysis (GEPIA) and Kaplan–Meier plotter bioinformatics, revealed a significant correlation between higher levels of HEPH expression and favorable prognosis, in both cancer histotypes. Moreover, TIMER web platform showed a statistically significant association between HEPH expression and cell elements belonging to the tumor microenvironment identified as endothelial cells and a subpopulation of cancer-associated fibroblasts, further confirmed by double immunohistochemical labeling with cell type specific markers. Taken together, these data shed a light on the complex mechanisms of local iron handling lung cancer can exploit to support tumorigenesis.
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This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Oncology
Reviewed by: Gregory Jon Anderson, The University of Queensland, Australia; Manfred Nairz, Innsbruck Medical University, Austria
These authors have contributed equally to this work
Edited by: Khashayarsha Khazaie, Mayo Clinic College of Medicine and Science, United States
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2021.638856