Establishment and characterization of a novel cancer stem‐like cell of cholangiocarcinoma
Cholangiocarcinoma (CCA) is an aggressive malignant tumor of bile duct epithelia. Recent evidence suggests the impact of cancer stem cells (CSC) on the therapeutic resistance of CCA; however, the knowledge of CSC in CCA is limited due to the lack of a CSC model. In this study, we successfully establ...
Gespeichert in:
Veröffentlicht in: | Cancer science 2023-08, Vol.114 (8), p.3230-3246 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 3246 |
---|---|
container_issue | 8 |
container_start_page | 3230 |
container_title | Cancer science |
container_volume | 114 |
creator | Panawan, Orasa Silsirivanit, Atit Chang, Chih‐Hsiang Putthisen, Siyaporn Boonnate, Piyanard Yokota, Taro Nishisyama‐Ikeda, Yuki Detarya, Marutpong Sawanyawisuth, Kanlayanee Kaewkong, Worasak Muisuk, Kanha Luang, Sukanya Vaeteewoottacharn, Kulthida Kariya, Ryusho Yano, Hiromu Komohara, Yoshihiro Ohta, Kunimasa Okada, Seiji Wongkham, Sopit Araki, Norie |
description | Cholangiocarcinoma (CCA) is an aggressive malignant tumor of bile duct epithelia. Recent evidence suggests the impact of cancer stem cells (CSC) on the therapeutic resistance of CCA; however, the knowledge of CSC in CCA is limited due to the lack of a CSC model. In this study, we successfully established a stable sphere‐forming CCA stem‐like cell, KKU‐055‐CSC, from the original CCA cell line, KKU‐055. The KKU‐055‐CSC exhibits CSC characteristics, including: (1) the ability to grow stably and withstand continuous passage for a long period of culture in the stem cell medium, (2) high expression of stem cell markers, (3) low responsiveness to standard chemotherapy drugs, (4) multilineage differentiation, and (5) faster and constant expansive tumor formation in xenograft mouse models. To identify the CCA‐CSC‐associated pathway, we have undertaken a global proteomics and functional cluster/network analysis. Proteomics identified the 5925 proteins in total, and the significantly upregulated proteins in CSC compared with FCS‐induced differentiated CSC and its parental cells were extracted. Network analysis revealed that high mobility group A1 (HMGA1) and Aurora A signaling through the signal transducer and activator of transcription 3 pathways were enriched in KKU‐055‐CSC. Knockdown of HMGA1 in KKU‐055‐CSC suppressed the expression of stem cell markers, induced the differentiation followed by cell proliferation, and enhanced sensitivity to chemotherapy drugs including Aurora A inhibitors. In silico analysis indicated that the expression of HMGA1 was correlated with Aurora A expressions and poor survival of CCA patients. In conclusion, we have established a unique CCA stem‐like cell model and identified the HMGA1‐Aurora A signaling as an important pathway for CSC‐CCA.
A novel cancer stem‐like cell, KKU‐055‐CSC, was established from a cholangiocarcinoma cell line. The cell exhibits stem cell properties and could be a representative clone of cholangiocarcinoma (CCA) cancer stem cells (CSC). Using this cell, HMGA1‐Aurora A signaling was identified as an important pathway for CSC‐CCA. |
doi_str_mv | 10.1111/cas.15812 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10394157</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2844434995</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4682-3d6c6ac35e6af8fd017e8d40dad3b4257593cd16a4a14460754dd6504e2001573</originalsourceid><addsrcrecordid>eNp1kc1OFTEYhhuiEUQX3ACZxA0uBvrfmRUhJ_iTkLhQVy6a77QdTqHTQjsHgysvwWv0SuxhgKCJ3bRJnzz53u9FaI_gQ1LPkYFySERH6BbaIYz3rcJYPrt7q7bHjG6jl6VcYMwk7_kLtM0UplJQtYO-nZYJlsGX1eji1EC0jVlBBjO57H_A5FNs0tBAE9ONC42BaFxuyuTG3z9_BX_pGuNC2CBmlQLEc58MZONjGuEVej5AKO71_b2Lvr47_bL40J59ev9xcXLWGi472jIrjQTDhJMwdIPFRLnOcmzBsiWnQomeGUskcCCcS6wEt1YKzB3FmAjFdtHx7L1aL0dnTQ2SIeir7EfItzqB13__RL_S5-lGE8x6PhsO7g05Xa9dmfToyyYYRJfWRVPVd4rQjtKKvvkHvUjrHGs-TTvOeV1_Lyr1dqZMTqVkNzxOQ7DedKZrZ_qus8ruPx3_kXwoqQJHM_DdB3f7f5NenHyelX8AYsmh9Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2844434995</pqid></control><display><type>article</type><title>Establishment and characterization of a novel cancer stem‐like cell of cholangiocarcinoma</title><source>MEDLINE</source><source>Wiley Online Library Open Access</source><source>DOAJ Directory of Open Access Journals</source><source>Wiley Online Library Journals Frontfile Complete</source><source>PubMed Central</source><creator>Panawan, Orasa ; Silsirivanit, Atit ; Chang, Chih‐Hsiang ; Putthisen, Siyaporn ; Boonnate, Piyanard ; Yokota, Taro ; Nishisyama‐Ikeda, Yuki ; Detarya, Marutpong ; Sawanyawisuth, Kanlayanee ; Kaewkong, Worasak ; Muisuk, Kanha ; Luang, Sukanya ; Vaeteewoottacharn, Kulthida ; Kariya, Ryusho ; Yano, Hiromu ; Komohara, Yoshihiro ; Ohta, Kunimasa ; Okada, Seiji ; Wongkham, Sopit ; Araki, Norie</creator><creatorcontrib>Panawan, Orasa ; Silsirivanit, Atit ; Chang, Chih‐Hsiang ; Putthisen, Siyaporn ; Boonnate, Piyanard ; Yokota, Taro ; Nishisyama‐Ikeda, Yuki ; Detarya, Marutpong ; Sawanyawisuth, Kanlayanee ; Kaewkong, Worasak ; Muisuk, Kanha ; Luang, Sukanya ; Vaeteewoottacharn, Kulthida ; Kariya, Ryusho ; Yano, Hiromu ; Komohara, Yoshihiro ; Ohta, Kunimasa ; Okada, Seiji ; Wongkham, Sopit ; Araki, Norie</creatorcontrib><description>Cholangiocarcinoma (CCA) is an aggressive malignant tumor of bile duct epithelia. Recent evidence suggests the impact of cancer stem cells (CSC) on the therapeutic resistance of CCA; however, the knowledge of CSC in CCA is limited due to the lack of a CSC model. In this study, we successfully established a stable sphere‐forming CCA stem‐like cell, KKU‐055‐CSC, from the original CCA cell line, KKU‐055. The KKU‐055‐CSC exhibits CSC characteristics, including: (1) the ability to grow stably and withstand continuous passage for a long period of culture in the stem cell medium, (2) high expression of stem cell markers, (3) low responsiveness to standard chemotherapy drugs, (4) multilineage differentiation, and (5) faster and constant expansive tumor formation in xenograft mouse models. To identify the CCA‐CSC‐associated pathway, we have undertaken a global proteomics and functional cluster/network analysis. Proteomics identified the 5925 proteins in total, and the significantly upregulated proteins in CSC compared with FCS‐induced differentiated CSC and its parental cells were extracted. Network analysis revealed that high mobility group A1 (HMGA1) and Aurora A signaling through the signal transducer and activator of transcription 3 pathways were enriched in KKU‐055‐CSC. Knockdown of HMGA1 in KKU‐055‐CSC suppressed the expression of stem cell markers, induced the differentiation followed by cell proliferation, and enhanced sensitivity to chemotherapy drugs including Aurora A inhibitors. In silico analysis indicated that the expression of HMGA1 was correlated with Aurora A expressions and poor survival of CCA patients. In conclusion, we have established a unique CCA stem‐like cell model and identified the HMGA1‐Aurora A signaling as an important pathway for CSC‐CCA.
A novel cancer stem‐like cell, KKU‐055‐CSC, was established from a cholangiocarcinoma cell line. The cell exhibits stem cell properties and could be a representative clone of cholangiocarcinoma (CCA) cancer stem cells (CSC). Using this cell, HMGA1‐Aurora A signaling was identified as an important pathway for CSC‐CCA.</description><identifier>ISSN: 1347-9032</identifier><identifier>EISSN: 1349-7006</identifier><identifier>DOI: 10.1111/cas.15812</identifier><identifier>PMID: 37026527</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Animal models ; Animals ; bile duct ; Bile Duct Neoplasms - metabolism ; Bile ducts ; Bile Ducts, Intrahepatic - metabolism ; Cancer ; cancer stem cell ; Cell culture ; Cell differentiation ; Cell Line, Tumor ; Cell Proliferation ; Chemotherapy ; Cholangiocarcinoma ; Cholangiocarcinoma - metabolism ; Chromosomes ; Experiments ; Growth factors ; HMGA1 ; HMGA1a Protein ; Humans ; liver ; Mice ; Neoplastic Stem Cells - metabolism ; Original ; ORIGINAL ARTICLES ; Preservatives ; Proteomics ; Signal transduction ; Spheres ; Stem cells ; Tumors</subject><ispartof>Cancer science, 2023-08, Vol.114 (8), p.3230-3246</ispartof><rights>2023 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.</rights><rights>2023 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.</rights><rights>2023. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4682-3d6c6ac35e6af8fd017e8d40dad3b4257593cd16a4a14460754dd6504e2001573</citedby><cites>FETCH-LOGICAL-c4682-3d6c6ac35e6af8fd017e8d40dad3b4257593cd16a4a14460754dd6504e2001573</cites><orcidid>0000-0001-9987-6229 ; 0000-0002-5777-3843 ; 0000-0001-9723-0846</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394157/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394157/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1411,11541,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37026527$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Panawan, Orasa</creatorcontrib><creatorcontrib>Silsirivanit, Atit</creatorcontrib><creatorcontrib>Chang, Chih‐Hsiang</creatorcontrib><creatorcontrib>Putthisen, Siyaporn</creatorcontrib><creatorcontrib>Boonnate, Piyanard</creatorcontrib><creatorcontrib>Yokota, Taro</creatorcontrib><creatorcontrib>Nishisyama‐Ikeda, Yuki</creatorcontrib><creatorcontrib>Detarya, Marutpong</creatorcontrib><creatorcontrib>Sawanyawisuth, Kanlayanee</creatorcontrib><creatorcontrib>Kaewkong, Worasak</creatorcontrib><creatorcontrib>Muisuk, Kanha</creatorcontrib><creatorcontrib>Luang, Sukanya</creatorcontrib><creatorcontrib>Vaeteewoottacharn, Kulthida</creatorcontrib><creatorcontrib>Kariya, Ryusho</creatorcontrib><creatorcontrib>Yano, Hiromu</creatorcontrib><creatorcontrib>Komohara, Yoshihiro</creatorcontrib><creatorcontrib>Ohta, Kunimasa</creatorcontrib><creatorcontrib>Okada, Seiji</creatorcontrib><creatorcontrib>Wongkham, Sopit</creatorcontrib><creatorcontrib>Araki, Norie</creatorcontrib><title>Establishment and characterization of a novel cancer stem‐like cell of cholangiocarcinoma</title><title>Cancer science</title><addtitle>Cancer Sci</addtitle><description>Cholangiocarcinoma (CCA) is an aggressive malignant tumor of bile duct epithelia. Recent evidence suggests the impact of cancer stem cells (CSC) on the therapeutic resistance of CCA; however, the knowledge of CSC in CCA is limited due to the lack of a CSC model. In this study, we successfully established a stable sphere‐forming CCA stem‐like cell, KKU‐055‐CSC, from the original CCA cell line, KKU‐055. The KKU‐055‐CSC exhibits CSC characteristics, including: (1) the ability to grow stably and withstand continuous passage for a long period of culture in the stem cell medium, (2) high expression of stem cell markers, (3) low responsiveness to standard chemotherapy drugs, (4) multilineage differentiation, and (5) faster and constant expansive tumor formation in xenograft mouse models. To identify the CCA‐CSC‐associated pathway, we have undertaken a global proteomics and functional cluster/network analysis. Proteomics identified the 5925 proteins in total, and the significantly upregulated proteins in CSC compared with FCS‐induced differentiated CSC and its parental cells were extracted. Network analysis revealed that high mobility group A1 (HMGA1) and Aurora A signaling through the signal transducer and activator of transcription 3 pathways were enriched in KKU‐055‐CSC. Knockdown of HMGA1 in KKU‐055‐CSC suppressed the expression of stem cell markers, induced the differentiation followed by cell proliferation, and enhanced sensitivity to chemotherapy drugs including Aurora A inhibitors. In silico analysis indicated that the expression of HMGA1 was correlated with Aurora A expressions and poor survival of CCA patients. In conclusion, we have established a unique CCA stem‐like cell model and identified the HMGA1‐Aurora A signaling as an important pathway for CSC‐CCA.
A novel cancer stem‐like cell, KKU‐055‐CSC, was established from a cholangiocarcinoma cell line. The cell exhibits stem cell properties and could be a representative clone of cholangiocarcinoma (CCA) cancer stem cells (CSC). Using this cell, HMGA1‐Aurora A signaling was identified as an important pathway for CSC‐CCA.</description><subject>Animal models</subject><subject>Animals</subject><subject>bile duct</subject><subject>Bile Duct Neoplasms - metabolism</subject><subject>Bile ducts</subject><subject>Bile Ducts, Intrahepatic - metabolism</subject><subject>Cancer</subject><subject>cancer stem cell</subject><subject>Cell culture</subject><subject>Cell differentiation</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Chemotherapy</subject><subject>Cholangiocarcinoma</subject><subject>Cholangiocarcinoma - metabolism</subject><subject>Chromosomes</subject><subject>Experiments</subject><subject>Growth factors</subject><subject>HMGA1</subject><subject>HMGA1a Protein</subject><subject>Humans</subject><subject>liver</subject><subject>Mice</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Original</subject><subject>ORIGINAL ARTICLES</subject><subject>Preservatives</subject><subject>Proteomics</subject><subject>Signal transduction</subject><subject>Spheres</subject><subject>Stem cells</subject><subject>Tumors</subject><issn>1347-9032</issn><issn>1349-7006</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kc1OFTEYhhuiEUQX3ACZxA0uBvrfmRUhJ_iTkLhQVy6a77QdTqHTQjsHgysvwWv0SuxhgKCJ3bRJnzz53u9FaI_gQ1LPkYFySERH6BbaIYz3rcJYPrt7q7bHjG6jl6VcYMwk7_kLtM0UplJQtYO-nZYJlsGX1eji1EC0jVlBBjO57H_A5FNs0tBAE9ONC42BaFxuyuTG3z9_BX_pGuNC2CBmlQLEc58MZONjGuEVej5AKO71_b2Lvr47_bL40J59ev9xcXLWGi472jIrjQTDhJMwdIPFRLnOcmzBsiWnQomeGUskcCCcS6wEt1YKzB3FmAjFdtHx7L1aL0dnTQ2SIeir7EfItzqB13__RL_S5-lGE8x6PhsO7g05Xa9dmfToyyYYRJfWRVPVd4rQjtKKvvkHvUjrHGs-TTvOeV1_Lyr1dqZMTqVkNzxOQ7DedKZrZ_qus8ruPx3_kXwoqQJHM_DdB3f7f5NenHyelX8AYsmh9Q</recordid><startdate>202308</startdate><enddate>202308</enddate><creator>Panawan, Orasa</creator><creator>Silsirivanit, Atit</creator><creator>Chang, Chih‐Hsiang</creator><creator>Putthisen, Siyaporn</creator><creator>Boonnate, Piyanard</creator><creator>Yokota, Taro</creator><creator>Nishisyama‐Ikeda, Yuki</creator><creator>Detarya, Marutpong</creator><creator>Sawanyawisuth, Kanlayanee</creator><creator>Kaewkong, Worasak</creator><creator>Muisuk, Kanha</creator><creator>Luang, Sukanya</creator><creator>Vaeteewoottacharn, Kulthida</creator><creator>Kariya, Ryusho</creator><creator>Yano, Hiromu</creator><creator>Komohara, Yoshihiro</creator><creator>Ohta, Kunimasa</creator><creator>Okada, Seiji</creator><creator>Wongkham, Sopit</creator><creator>Araki, Norie</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9987-6229</orcidid><orcidid>https://orcid.org/0000-0002-5777-3843</orcidid><orcidid>https://orcid.org/0000-0001-9723-0846</orcidid></search><sort><creationdate>202308</creationdate><title>Establishment and characterization of a novel cancer stem‐like cell of cholangiocarcinoma</title><author>Panawan, Orasa ; Silsirivanit, Atit ; Chang, Chih‐Hsiang ; Putthisen, Siyaporn ; Boonnate, Piyanard ; Yokota, Taro ; Nishisyama‐Ikeda, Yuki ; Detarya, Marutpong ; Sawanyawisuth, Kanlayanee ; Kaewkong, Worasak ; Muisuk, Kanha ; Luang, Sukanya ; Vaeteewoottacharn, Kulthida ; Kariya, Ryusho ; Yano, Hiromu ; Komohara, Yoshihiro ; Ohta, Kunimasa ; Okada, Seiji ; Wongkham, Sopit ; Araki, Norie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4682-3d6c6ac35e6af8fd017e8d40dad3b4257593cd16a4a14460754dd6504e2001573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>bile duct</topic><topic>Bile Duct Neoplasms - metabolism</topic><topic>Bile ducts</topic><topic>Bile Ducts, Intrahepatic - metabolism</topic><topic>Cancer</topic><topic>cancer stem cell</topic><topic>Cell culture</topic><topic>Cell differentiation</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>Chemotherapy</topic><topic>Cholangiocarcinoma</topic><topic>Cholangiocarcinoma - metabolism</topic><topic>Chromosomes</topic><topic>Experiments</topic><topic>Growth factors</topic><topic>HMGA1</topic><topic>HMGA1a Protein</topic><topic>Humans</topic><topic>liver</topic><topic>Mice</topic><topic>Neoplastic Stem Cells - metabolism</topic><topic>Original</topic><topic>ORIGINAL ARTICLES</topic><topic>Preservatives</topic><topic>Proteomics</topic><topic>Signal transduction</topic><topic>Spheres</topic><topic>Stem cells</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Panawan, Orasa</creatorcontrib><creatorcontrib>Silsirivanit, Atit</creatorcontrib><creatorcontrib>Chang, Chih‐Hsiang</creatorcontrib><creatorcontrib>Putthisen, Siyaporn</creatorcontrib><creatorcontrib>Boonnate, Piyanard</creatorcontrib><creatorcontrib>Yokota, Taro</creatorcontrib><creatorcontrib>Nishisyama‐Ikeda, Yuki</creatorcontrib><creatorcontrib>Detarya, Marutpong</creatorcontrib><creatorcontrib>Sawanyawisuth, Kanlayanee</creatorcontrib><creatorcontrib>Kaewkong, Worasak</creatorcontrib><creatorcontrib>Muisuk, Kanha</creatorcontrib><creatorcontrib>Luang, Sukanya</creatorcontrib><creatorcontrib>Vaeteewoottacharn, Kulthida</creatorcontrib><creatorcontrib>Kariya, Ryusho</creatorcontrib><creatorcontrib>Yano, Hiromu</creatorcontrib><creatorcontrib>Komohara, Yoshihiro</creatorcontrib><creatorcontrib>Ohta, Kunimasa</creatorcontrib><creatorcontrib>Okada, Seiji</creatorcontrib><creatorcontrib>Wongkham, Sopit</creatorcontrib><creatorcontrib>Araki, Norie</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Panawan, Orasa</au><au>Silsirivanit, Atit</au><au>Chang, Chih‐Hsiang</au><au>Putthisen, Siyaporn</au><au>Boonnate, Piyanard</au><au>Yokota, Taro</au><au>Nishisyama‐Ikeda, Yuki</au><au>Detarya, Marutpong</au><au>Sawanyawisuth, Kanlayanee</au><au>Kaewkong, Worasak</au><au>Muisuk, Kanha</au><au>Luang, Sukanya</au><au>Vaeteewoottacharn, Kulthida</au><au>Kariya, Ryusho</au><au>Yano, Hiromu</au><au>Komohara, Yoshihiro</au><au>Ohta, Kunimasa</au><au>Okada, Seiji</au><au>Wongkham, Sopit</au><au>Araki, Norie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Establishment and characterization of a novel cancer stem‐like cell of cholangiocarcinoma</atitle><jtitle>Cancer science</jtitle><addtitle>Cancer Sci</addtitle><date>2023-08</date><risdate>2023</risdate><volume>114</volume><issue>8</issue><spage>3230</spage><epage>3246</epage><pages>3230-3246</pages><issn>1347-9032</issn><eissn>1349-7006</eissn><abstract>Cholangiocarcinoma (CCA) is an aggressive malignant tumor of bile duct epithelia. Recent evidence suggests the impact of cancer stem cells (CSC) on the therapeutic resistance of CCA; however, the knowledge of CSC in CCA is limited due to the lack of a CSC model. In this study, we successfully established a stable sphere‐forming CCA stem‐like cell, KKU‐055‐CSC, from the original CCA cell line, KKU‐055. The KKU‐055‐CSC exhibits CSC characteristics, including: (1) the ability to grow stably and withstand continuous passage for a long period of culture in the stem cell medium, (2) high expression of stem cell markers, (3) low responsiveness to standard chemotherapy drugs, (4) multilineage differentiation, and (5) faster and constant expansive tumor formation in xenograft mouse models. To identify the CCA‐CSC‐associated pathway, we have undertaken a global proteomics and functional cluster/network analysis. Proteomics identified the 5925 proteins in total, and the significantly upregulated proteins in CSC compared with FCS‐induced differentiated CSC and its parental cells were extracted. Network analysis revealed that high mobility group A1 (HMGA1) and Aurora A signaling through the signal transducer and activator of transcription 3 pathways were enriched in KKU‐055‐CSC. Knockdown of HMGA1 in KKU‐055‐CSC suppressed the expression of stem cell markers, induced the differentiation followed by cell proliferation, and enhanced sensitivity to chemotherapy drugs including Aurora A inhibitors. In silico analysis indicated that the expression of HMGA1 was correlated with Aurora A expressions and poor survival of CCA patients. In conclusion, we have established a unique CCA stem‐like cell model and identified the HMGA1‐Aurora A signaling as an important pathway for CSC‐CCA.
A novel cancer stem‐like cell, KKU‐055‐CSC, was established from a cholangiocarcinoma cell line. The cell exhibits stem cell properties and could be a representative clone of cholangiocarcinoma (CCA) cancer stem cells (CSC). Using this cell, HMGA1‐Aurora A signaling was identified as an important pathway for CSC‐CCA.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>37026527</pmid><doi>10.1111/cas.15812</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0001-9987-6229</orcidid><orcidid>https://orcid.org/0000-0002-5777-3843</orcidid><orcidid>https://orcid.org/0000-0001-9723-0846</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1347-9032 |
ispartof | Cancer science, 2023-08, Vol.114 (8), p.3230-3246 |
issn | 1347-9032 1349-7006 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10394157 |
source | MEDLINE; Wiley Online Library Open Access; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; PubMed Central |
subjects | Animal models Animals bile duct Bile Duct Neoplasms - metabolism Bile ducts Bile Ducts, Intrahepatic - metabolism Cancer cancer stem cell Cell culture Cell differentiation Cell Line, Tumor Cell Proliferation Chemotherapy Cholangiocarcinoma Cholangiocarcinoma - metabolism Chromosomes Experiments Growth factors HMGA1 HMGA1a Protein Humans liver Mice Neoplastic Stem Cells - metabolism Original ORIGINAL ARTICLES Preservatives Proteomics Signal transduction Spheres Stem cells Tumors |
title | Establishment and characterization of a novel cancer stem‐like cell of cholangiocarcinoma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T14%3A01%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Establishment%20and%20characterization%20of%20a%20novel%20cancer%20stem%E2%80%90like%20cell%20of%20cholangiocarcinoma&rft.jtitle=Cancer%20science&rft.au=Panawan,%20Orasa&rft.date=2023-08&rft.volume=114&rft.issue=8&rft.spage=3230&rft.epage=3246&rft.pages=3230-3246&rft.issn=1347-9032&rft.eissn=1349-7006&rft_id=info:doi/10.1111/cas.15812&rft_dat=%3Cproquest_pubme%3E2844434995%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2844434995&rft_id=info:pmid/37026527&rfr_iscdi=true |