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Claudin and pancreatic cancer
Due to the lack of timely and accurate screening modalities and treatments, most pancreatic cancer (PCa) patients undergo fatal PCa progression within a short period since diagnosis. The claudin(CLDN) family is expressed specifically as tight junction structure in a variety of tumors, including PCa,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027734/ https://www.ncbi.nlm.nih.gov/pubmed/36959784 http://dx.doi.org/10.3389/fonc.2023.1136227 |
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author | Wang, Chen Wu, Na Pei, Beibei Ma, Xiaoyan Yang, Wenhui |
author_facet | Wang, Chen Wu, Na Pei, Beibei Ma, Xiaoyan Yang, Wenhui |
author_sort | Wang, Chen |
collection | PubMed |
description | Due to the lack of timely and accurate screening modalities and treatments, most pancreatic cancer (PCa) patients undergo fatal PCa progression within a short period since diagnosis. The claudin(CLDN) family is expressed specifically as tight junction structure in a variety of tumors, including PCa, and affects tumor progression by changing the cell junctions. Thus far, many of the 27 members of the claudin family, including claudin-18.2 and claudin-4, have significantly aberrantly expression in pancreatic tumors. In addition, some studies have confirmed the role of some claudin proteins in the diagnosis and treatment of pancreatic tumors. By targeting different targets of claudin protein and combining chemotherapy, further enhance tumor cell necrosis and inhibit tumor invasion and metastasis. Claudins can either promote or inhibit the development of pancreatic cancer, which indicates that the diagnosis and treatment of different kinds of claudins require to consider different biological characteristics. This literature summarizes the functional characteristics and clinical applications of various claudin proteins in Pca cells, with a focus on claudin-18.2 and claudin-4. |
format | Online Article Text |
id | pubmed-10027734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100277342023-03-22 Claudin and pancreatic cancer Wang, Chen Wu, Na Pei, Beibei Ma, Xiaoyan Yang, Wenhui Front Oncol Oncology Due to the lack of timely and accurate screening modalities and treatments, most pancreatic cancer (PCa) patients undergo fatal PCa progression within a short period since diagnosis. The claudin(CLDN) family is expressed specifically as tight junction structure in a variety of tumors, including PCa, and affects tumor progression by changing the cell junctions. Thus far, many of the 27 members of the claudin family, including claudin-18.2 and claudin-4, have significantly aberrantly expression in pancreatic tumors. In addition, some studies have confirmed the role of some claudin proteins in the diagnosis and treatment of pancreatic tumors. By targeting different targets of claudin protein and combining chemotherapy, further enhance tumor cell necrosis and inhibit tumor invasion and metastasis. Claudins can either promote or inhibit the development of pancreatic cancer, which indicates that the diagnosis and treatment of different kinds of claudins require to consider different biological characteristics. This literature summarizes the functional characteristics and clinical applications of various claudin proteins in Pca cells, with a focus on claudin-18.2 and claudin-4. Frontiers Media S.A. 2023-03-07 /pmc/articles/PMC10027734/ /pubmed/36959784 http://dx.doi.org/10.3389/fonc.2023.1136227 Text en Copyright © 2023 Wang, Wu, Pei, Ma and Yang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Wang, Chen Wu, Na Pei, Beibei Ma, Xiaoyan Yang, Wenhui Claudin and pancreatic cancer |
title | Claudin and pancreatic cancer |
title_full | Claudin and pancreatic cancer |
title_fullStr | Claudin and pancreatic cancer |
title_full_unstemmed | Claudin and pancreatic cancer |
title_short | Claudin and pancreatic cancer |
title_sort | claudin and pancreatic cancer |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027734/ https://www.ncbi.nlm.nih.gov/pubmed/36959784 http://dx.doi.org/10.3389/fonc.2023.1136227 |
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