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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...

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Detalles Bibliográficos
Autores principales: Nonboe, Annika W., Bald, Zuzanna H., Vogel, Lotte K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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
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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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