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Anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer

Claudin-4 (CLDN4) is a major epithelial tight junction protein overexpressed in many cancers to maintain the tumor environment. In this report, we aimed to determine the efficacy of targeting CLDN4 in colorectal cancer (CRC) using an anti-CLDN4 extracellular domain antibody, 4D3. CLDN4 was upregulat...

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Autores principales: Fujiwara-Tani, Rina, Sasaki, Takamitsu, Luo, Yi, Goto, Kei, Kawahara, Isao, Nishiguchi, Yukiko, Kishi, Shingo, Mori, Shiori, Ohmori, Hitoshi, Kondoh, Masuo, Kuniyasu, Hiroki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324772/
https://www.ncbi.nlm.nih.gov/pubmed/30647838
http://dx.doi.org/10.18632/oncotarget.26427
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author Fujiwara-Tani, Rina
Sasaki, Takamitsu
Luo, Yi
Goto, Kei
Kawahara, Isao
Nishiguchi, Yukiko
Kishi, Shingo
Mori, Shiori
Ohmori, Hitoshi
Kondoh, Masuo
Kuniyasu, Hiroki
author_facet Fujiwara-Tani, Rina
Sasaki, Takamitsu
Luo, Yi
Goto, Kei
Kawahara, Isao
Nishiguchi, Yukiko
Kishi, Shingo
Mori, Shiori
Ohmori, Hitoshi
Kondoh, Masuo
Kuniyasu, Hiroki
author_sort Fujiwara-Tani, Rina
collection PubMed
description Claudin-4 (CLDN4) is a major epithelial tight junction protein overexpressed in many cancers to maintain the tumor environment. In this report, we aimed to determine the efficacy of targeting CLDN4 in colorectal cancer (CRC) using an anti-CLDN4 extracellular domain antibody, 4D3. CLDN4 was upregulated in CRC metastatic foci. CLDN4 expression in CRC cells was reduced by upregulation of TNFα, which was induced by Clostridium perfringens enterotoxin produced by gut flora. In a nude mouse liver metastasis model, inhibition of metastasis was increased by combination treatment with 5-fluorouracil (FU) and 4D3 compared to that with 5-FU alone. Moreover, combination treatment with 4D3 and anti-epithelial growth factor receptor (EGFR) antibody C225 resulted in more pronounced inhibition of in vitro sphere formation and tumor growth in nude mice compared to that observed with C225 alone. Moreover, the time interval between the administration of 4D3 and that of C225 was important for maximizing the C225-induced inhibition of EGFR phosphorylation. In a nude mouse model, sequential treatment with 4D3 and C225 with a 6-h time interval resulted in more pronounced inhibition of tumor growth than concurrent treatment. These findings suggest that the targeting of CLDN4 enhances the antitumoral effects of chemotherapeutic agents and molecular targeting antibodies when used in combination.
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spelling pubmed-63247722019-01-15 Anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer Fujiwara-Tani, Rina Sasaki, Takamitsu Luo, Yi Goto, Kei Kawahara, Isao Nishiguchi, Yukiko Kishi, Shingo Mori, Shiori Ohmori, Hitoshi Kondoh, Masuo Kuniyasu, Hiroki Oncotarget Research Paper Claudin-4 (CLDN4) is a major epithelial tight junction protein overexpressed in many cancers to maintain the tumor environment. In this report, we aimed to determine the efficacy of targeting CLDN4 in colorectal cancer (CRC) using an anti-CLDN4 extracellular domain antibody, 4D3. CLDN4 was upregulated in CRC metastatic foci. CLDN4 expression in CRC cells was reduced by upregulation of TNFα, which was induced by Clostridium perfringens enterotoxin produced by gut flora. In a nude mouse liver metastasis model, inhibition of metastasis was increased by combination treatment with 5-fluorouracil (FU) and 4D3 compared to that with 5-FU alone. Moreover, combination treatment with 4D3 and anti-epithelial growth factor receptor (EGFR) antibody C225 resulted in more pronounced inhibition of in vitro sphere formation and tumor growth in nude mice compared to that observed with C225 alone. Moreover, the time interval between the administration of 4D3 and that of C225 was important for maximizing the C225-induced inhibition of EGFR phosphorylation. In a nude mouse model, sequential treatment with 4D3 and C225 with a 6-h time interval resulted in more pronounced inhibition of tumor growth than concurrent treatment. These findings suggest that the targeting of CLDN4 enhances the antitumoral effects of chemotherapeutic agents and molecular targeting antibodies when used in combination. Impact Journals LLC 2018-12-21 /pmc/articles/PMC6324772/ /pubmed/30647838 http://dx.doi.org/10.18632/oncotarget.26427 Text en Copyright: © 2018 Fujiwara-Tani et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Fujiwara-Tani, Rina
Sasaki, Takamitsu
Luo, Yi
Goto, Kei
Kawahara, Isao
Nishiguchi, Yukiko
Kishi, Shingo
Mori, Shiori
Ohmori, Hitoshi
Kondoh, Masuo
Kuniyasu, Hiroki
Anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer
title Anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer
title_full Anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer
title_fullStr Anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer
title_full_unstemmed Anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer
title_short Anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer
title_sort anti-claudin-4 extracellular domain antibody enhances the antitumoral effects of chemotherapeutic and antibody drugs in colorectal cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324772/
https://www.ncbi.nlm.nih.gov/pubmed/30647838
http://dx.doi.org/10.18632/oncotarget.26427
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