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...

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Veröffentlicht in:Cancer science 2023-08, Vol.114 (8), p.3230-3246
Hauptverfasser: 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
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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
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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 &amp; 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 &amp; Sons Australia, Ltd on behalf of Japanese Cancer Association.</rights><rights>2023 The Authors. 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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 &amp; 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 - 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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 &amp; 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>
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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
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