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Understanding HAIs: Ally proteins in the fight against cancer
Understanding how HAI‐1 and HAI‐2 regulate the epithelial serine protease matriptase may hold the key to curing epithelial‐derived cancer. HAIs are serine protease inhibitors that inhibit matriptase and have a poorly understood effect on the presence of matriptase protein in cells. In this issue of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305204/ https://www.ncbi.nlm.nih.gov/pubmed/35220685 http://dx.doi.org/10.1111/febs.16399 |
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author | Nonboe, Annika W. Bald, Zuzanna H. Vogel, Lotte K. |
author_facet | Nonboe, Annika W. Bald, Zuzanna H. Vogel, Lotte K. |
author_sort | Nonboe, Annika W. |
collection | PubMed |
description | Understanding how HAI‐1 and HAI‐2 regulate the epithelial serine protease matriptase may hold the key to curing epithelial‐derived cancer. HAIs are serine protease inhibitors that inhibit matriptase and have a poorly understood effect on the presence of matriptase protein in cells. In this issue of The FEBS Journal, Yamashita et al. provide much‐needed new insights into this effect, describing it as a ‘chaperone‐like function’ of HAI‐1. However, several observations suggest that matriptase folds correctly without HAIs and that HAIs are not chaperones. We introduce the concept of ‘ally proteins’ to categorize the poorly understood function of HAIs, distinguishing them from chaperones. Comment on: https://doi.org/10.1111/febs.16348 |
format | Online Article Text |
id | pubmed-9305204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93052042022-07-28 Understanding HAIs: Ally proteins in the fight against cancer Nonboe, Annika W. Bald, Zuzanna H. Vogel, Lotte K. FEBS J Commentaries Understanding how HAI‐1 and HAI‐2 regulate the epithelial serine protease matriptase may hold the key to curing epithelial‐derived cancer. HAIs are serine protease inhibitors that inhibit matriptase and have a poorly understood effect on the presence of matriptase protein in cells. In this issue of The FEBS Journal, Yamashita et al. provide much‐needed new insights into this effect, describing it as a ‘chaperone‐like function’ of HAI‐1. However, several observations suggest that matriptase folds correctly without HAIs and that HAIs are not chaperones. We introduce the concept of ‘ally proteins’ to categorize the poorly understood function of HAIs, distinguishing them from chaperones. Comment on: https://doi.org/10.1111/febs.16348 John Wiley and Sons Inc. 2022-02-27 2022-06 /pmc/articles/PMC9305204/ /pubmed/35220685 http://dx.doi.org/10.1111/febs.16399 Text en © 2022 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Commentaries Nonboe, Annika W. Bald, Zuzanna H. Vogel, Lotte K. Understanding HAIs: Ally proteins in the fight against cancer |
title | Understanding HAIs: Ally proteins in the fight against cancer |
title_full | Understanding HAIs: Ally proteins in the fight against cancer |
title_fullStr | Understanding HAIs: Ally proteins in the fight against cancer |
title_full_unstemmed | Understanding HAIs: Ally proteins in the fight against cancer |
title_short | Understanding HAIs: Ally proteins in the fight against cancer |
title_sort | understanding hais: ally proteins in the fight against cancer |
topic | Commentaries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305204/ https://www.ncbi.nlm.nih.gov/pubmed/35220685 http://dx.doi.org/10.1111/febs.16399 |
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