Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/26327
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dc.contributor.authorKerslake, R-
dc.contributor.authorRandeva, HS-
dc.contributor.authorJonigk, D-
dc.contributor.authorWerlein, C-
dc.contributor.authorRobertus, JL-
dc.contributor.authorKatopodis, P-
dc.contributor.authorJasker, P-
dc.contributor.authorSpandidos, DA-
dc.contributor.authorKyrou, I-
dc.contributor.authorKarteris, E-
dc.date.accessioned2023-04-27T15:25:37Z-
dc.date.available2022-02-24-
dc.date.available2023-04-27T15:25:37Z-
dc.date.issued2022-02-24-
dc.identifierORCID iD: Emmanouil Karteris https://orcid.org/0000-0003-3231-7267-
dc.identifier138-
dc.identifier.citationKerslake, R. et al. (2022) 'Protein expression of transmembrane protease serine 4 in the gastrointestinal tract and in healthy, cancer, and SARS‑CoV‑2 infected lungs', Molecular medicine reports, 25 (4), 138, pp. 1 - 6. doi: 10.3892/mmr.2022.12654.en_US
dc.identifier.issn1791-2997-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/26327-
dc.descriptionAvailability of data and materials: The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.en_US
dc.description.abstractCopyright: © Kerslake et al. In addition to the angiotensin‑converting enzyme 2 (ACE2), a number of host cell entry mediators have been identified for severe acute respiratory syndrome coronavirus‑2 (SARS‑CoV‑2), including transmembrane protease serine 4 (TMPRSS4). The authors have recently demonstrated the upregulation of TMPRSS4 in 11 different cancers, as well as its specific expression within the central nervous system using in silico tools. The present study aimed to expand the initial observations and, using immunohistochemistry, TMPRSS4 protein expression in the gastrointestinal (GI) tract and lungs was further mapped. Immunohistochemistry was performed on tissue arrays and lung tissues of patients with non‑small cell lung cancer with concurrent coronavirus disease 2019 (COVID‑19) infection using TMPRSS4 antibody. The results revealed that TMPRSS4 was abundantly expressed in the oesophagus, stomach, small intestine, jejunum, ileum, colon, liver and pancreas. Moreover, the extensive TMPRSS4 protein expression in the lungs of a deceased patient with COVID‑19 with chronic obstructive pulmonary disease and bronchial carcinoma, as well in the adjacent normal tissue, was demonstrated for the first time, at least to the best of our knowledge. On the whole, the immunohistochemistry data of the present study suggest that TMPRSS4 may be implicated in the broader (pulmonary and extra‑pulmonary) COVID‑19 symptomatology; thus, it may be responsible for the tropism of this coronavirus both in the GI tract and lungs.en_US
dc.description.sponsorshipCancer Treatment and Research Trust; University Hospitals Coventry and Warwickshire NHS Trust (grant no. 12899).en_US
dc.format.extent1 - 6-
dc.format.mediumPrint-Electronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherSpandidos Publicationsen_US
dc.rightsCopyright: © Kerslake et al. This is an open access article distributed under the terms of Creative Commons Attribution License.-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjecttransmembrane protease serine 4-
dc.subjectcoronavirus disease 2019-
dc.subjectsevere acute respiratory syndrome coronavirus‑2-
dc.subjecttropism-
dc.subjectgastrointestinal tract-
dc.subjectlung-
dc.titleProtein expression of transmembrane protease serine 4 in the gastrointestinal tract and in healthy, cancer, and SARS‑CoV‑2 infected lungsen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.3892/mmr.2022.12654-
dc.relation.isPartOfMolecular medicine reports-
pubs.issue4-
pubs.publication-statusPublished-
pubs.volume25-
dc.identifier.eissn1791-3004-
dc.rights.holderKerslake et al.-
Appears in Collections:Dept of Life Sciences Research Papers

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