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CCR7 Mediates Cell Invasion and Migration in Extrahepatic Cholangiocarcinoma by Inducing Epithelial-Mesenchymal Transition
The epithelial-mesenchymal transition (EMT) contributes to the metastatic cascade in various tumors. C-C chemokine receptor 7 (CCR7) interacts with its ligand, chemokine (C-C motif) ligand 19 (CCL19), to promote EMT. However, the association between EMT and CCR7 in extrahepatic cholangiocarcinoma (E...
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Published in: | Cancers 2023-03, Vol.15 (6), p.1878 |
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creator | Oba, Mitsunobu Nakanishi, Yoshitsugu Mitsuhashi, Tomoko Sasaki, Katsunori Hatanaka, Kanako C Sasaki, Masako Nange, Ayae Okumura, Asami Hayashi, Mariko Yoshida, Yusuke Nitta, Takeo Ueno, Takashi Yamada, Toru Ono, Masato Kuwabara, Shota Okamura, Keisuke Tsuchikawa, Takahiro Nakamura, Toru Noji, Takehiro Asano, Toshimichi Tanaka, Kimitaka Takayama, Kiyoshi Hatanaka, Yutaka Hirano, Satoshi |
description | The epithelial-mesenchymal transition (EMT) contributes to the metastatic cascade in various tumors. C-C chemokine receptor 7 (CCR7) interacts with its ligand, chemokine (C-C motif) ligand 19 (CCL19), to promote EMT. However, the association between EMT and CCR7 in extrahepatic cholangiocarcinoma (EHCC) remains unknown. This study aimed to elucidate the prognostic impact of CCR7 expression and its association with clinicopathological features and EMT in EHCC. The association between CCR7 expression and clinicopathological features and EMT status was examined via the immunohistochemical staining of tumor sections from 181 patients with perihilar cholangiocarcinoma. This association was then investigated in TFK-1 and EGI-1 EHCC cell lines. High-grade CCR7 expression was significantly associated with a large number of tumor buds, low E-cadherin expression, and poor overall survival. TFK-1 showed CCR7 expression, and Western blotting revealed E-cadherin downregulation and vimentin upregulation in response to CCL19 treatment. The wound healing and Transwell invasion assays revealed that the activation of CCR7 by CCL19 enhanced the migration and invasion of TFK-1 cells, which were abrogated by a CCR7 antagonist. These results suggest that a high CCR7 expression is associated with an adverse postoperative prognosis via EMT induction and that CCR7 may be a potential target for adjuvant therapy in EHCC. |
doi_str_mv | 10.3390/cancers15061878 |
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C-C chemokine receptor 7 (CCR7) interacts with its ligand, chemokine (C-C motif) ligand 19 (CCL19), to promote EMT. However, the association between EMT and CCR7 in extrahepatic cholangiocarcinoma (EHCC) remains unknown. This study aimed to elucidate the prognostic impact of CCR7 expression and its association with clinicopathological features and EMT in EHCC. The association between CCR7 expression and clinicopathological features and EMT status was examined via the immunohistochemical staining of tumor sections from 181 patients with perihilar cholangiocarcinoma. This association was then investigated in TFK-1 and EGI-1 EHCC cell lines. High-grade CCR7 expression was significantly associated with a large number of tumor buds, low E-cadherin expression, and poor overall survival. TFK-1 showed CCR7 expression, and Western blotting revealed E-cadherin downregulation and vimentin upregulation in response to CCL19 treatment. The wound healing and Transwell invasion assays revealed that the activation of CCR7 by CCL19 enhanced the migration and invasion of TFK-1 cells, which were abrogated by a CCR7 antagonist. These results suggest that a high CCR7 expression is associated with an adverse postoperative prognosis via EMT induction and that CCR7 may be a potential target for adjuvant therapy in EHCC.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15061878</identifier><identifier>PMID: 36980764</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Antigens ; Bile ducts ; Cancer ; CC chemokine receptors ; CCL19 protein ; CCR7 protein ; Cell differentiation ; Cell migration ; Cell receptors ; Chemokine receptors ; Chemokines ; Cholangiocarcinoma ; E-cadherin ; Health aspects ; Lymphatic system ; Medical prognosis ; Medical research ; Metastases ; Metastasis ; Molecular modelling ; Physiology ; Review boards ; Tumors ; Vimentin ; Western blotting ; Wound healing</subject><ispartof>Cancers, 2023-03, Vol.15 (6), p.1878</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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C-C chemokine receptor 7 (CCR7) interacts with its ligand, chemokine (C-C motif) ligand 19 (CCL19), to promote EMT. However, the association between EMT and CCR7 in extrahepatic cholangiocarcinoma (EHCC) remains unknown. This study aimed to elucidate the prognostic impact of CCR7 expression and its association with clinicopathological features and EMT in EHCC. The association between CCR7 expression and clinicopathological features and EMT status was examined via the immunohistochemical staining of tumor sections from 181 patients with perihilar cholangiocarcinoma. This association was then investigated in TFK-1 and EGI-1 EHCC cell lines. High-grade CCR7 expression was significantly associated with a large number of tumor buds, low E-cadherin expression, and poor overall survival. TFK-1 showed CCR7 expression, and Western blotting revealed E-cadherin downregulation and vimentin upregulation in response to CCL19 treatment. The wound healing and Transwell invasion assays revealed that the activation of CCR7 by CCL19 enhanced the migration and invasion of TFK-1 cells, which were abrogated by a CCR7 antagonist. These results suggest that a high CCR7 expression is associated with an adverse postoperative prognosis via EMT induction and that CCR7 may be a potential target for adjuvant therapy in EHCC.</description><subject>Antigens</subject><subject>Bile ducts</subject><subject>Cancer</subject><subject>CC chemokine receptors</subject><subject>CCL19 protein</subject><subject>CCR7 protein</subject><subject>Cell differentiation</subject><subject>Cell migration</subject><subject>Cell receptors</subject><subject>Chemokine receptors</subject><subject>Chemokines</subject><subject>Cholangiocarcinoma</subject><subject>E-cadherin</subject><subject>Health aspects</subject><subject>Lymphatic system</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Molecular modelling</subject><subject>Physiology</subject><subject>Review boards</subject><subject>Tumors</subject><subject>Vimentin</subject><subject>Western 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Mediates Cell Invasion and Migration in Extrahepatic Cholangiocarcinoma by Inducing Epithelial-Mesenchymal Transition</title><author>Oba, Mitsunobu ; Nakanishi, Yoshitsugu ; Mitsuhashi, Tomoko ; Sasaki, Katsunori ; Hatanaka, Kanako C ; Sasaki, Masako ; Nange, Ayae ; Okumura, Asami ; Hayashi, Mariko ; Yoshida, Yusuke ; Nitta, Takeo ; Ueno, Takashi ; Yamada, Toru ; Ono, Masato ; Kuwabara, Shota ; Okamura, Keisuke ; Tsuchikawa, Takahiro ; Nakamura, Toru ; Noji, Takehiro ; Asano, Toshimichi ; Tanaka, Kimitaka ; Takayama, Kiyoshi ; Hatanaka, Yutaka ; Hirano, Satoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c533t-324bc7d5348fc81d8032774fce346366452e5cd387a8864a83584a91a2f969953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antigens</topic><topic>Bile ducts</topic><topic>Cancer</topic><topic>CC chemokine receptors</topic><topic>CCL19 protein</topic><topic>CCR7 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Ayae</au><au>Okumura, Asami</au><au>Hayashi, Mariko</au><au>Yoshida, Yusuke</au><au>Nitta, Takeo</au><au>Ueno, Takashi</au><au>Yamada, Toru</au><au>Ono, Masato</au><au>Kuwabara, Shota</au><au>Okamura, Keisuke</au><au>Tsuchikawa, Takahiro</au><au>Nakamura, Toru</au><au>Noji, Takehiro</au><au>Asano, Toshimichi</au><au>Tanaka, Kimitaka</au><au>Takayama, Kiyoshi</au><au>Hatanaka, Yutaka</au><au>Hirano, Satoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CCR7 Mediates Cell Invasion and Migration in Extrahepatic Cholangiocarcinoma by Inducing Epithelial-Mesenchymal Transition</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2023-03-01</date><risdate>2023</risdate><volume>15</volume><issue>6</issue><spage>1878</spage><pages>1878-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>The epithelial-mesenchymal transition (EMT) contributes to the metastatic cascade in various tumors. C-C chemokine receptor 7 (CCR7) interacts with its ligand, chemokine (C-C motif) ligand 19 (CCL19), to promote EMT. However, the association between EMT and CCR7 in extrahepatic cholangiocarcinoma (EHCC) remains unknown. This study aimed to elucidate the prognostic impact of CCR7 expression and its association with clinicopathological features and EMT in EHCC. The association between CCR7 expression and clinicopathological features and EMT status was examined via the immunohistochemical staining of tumor sections from 181 patients with perihilar cholangiocarcinoma. This association was then investigated in TFK-1 and EGI-1 EHCC cell lines. High-grade CCR7 expression was significantly associated with a large number of tumor buds, low E-cadherin expression, and poor overall survival. TFK-1 showed CCR7 expression, and Western blotting revealed E-cadherin downregulation and vimentin upregulation in response to CCL19 treatment. The wound healing and Transwell invasion assays revealed that the activation of CCR7 by CCL19 enhanced the migration and invasion of TFK-1 cells, which were abrogated by a CCR7 antagonist. These results suggest that a high CCR7 expression is associated with an adverse postoperative prognosis via EMT induction and that CCR7 may be a potential target for adjuvant therapy in EHCC.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36980764</pmid><doi>10.3390/cancers15061878</doi><orcidid>https://orcid.org/0000-0001-9899-4581</orcidid><orcidid>https://orcid.org/0000-0003-3048-0685</orcidid><orcidid>https://orcid.org/0000-0003-3128-1477</orcidid><orcidid>https://orcid.org/0000-0001-9300-7751</orcidid><orcidid>https://orcid.org/0000-0002-3847-280X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Bile ducts Cancer CC chemokine receptors CCL19 protein CCR7 protein Cell differentiation Cell migration Cell receptors Chemokine receptors Chemokines Cholangiocarcinoma E-cadherin Health aspects Lymphatic system Medical prognosis Medical research Metastases Metastasis Molecular modelling Physiology Review boards Tumors Vimentin Western blotting Wound healing |
title | CCR7 Mediates Cell Invasion and Migration in Extrahepatic Cholangiocarcinoma by Inducing Epithelial-Mesenchymal Transition |
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