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CD48-expressing non-small-cell lung cancer cells are susceptible to natural killer cell–mediated cytotoxicity
The susceptibility of cancer cells to natural killer (NK) cell–mediated cytotoxicity depends on the balance of activating and inhibitory ligands expressed on their surface. Although many types of cancer cells are killed by NK cells, non-small-cell lung cancer (NSCLC) cells are relatively resistant t...
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Published in: | Archives of pharmacal research 2022, 45(1), , pp.1-10 |
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description | The susceptibility of cancer cells to natural killer (NK) cell–mediated cytotoxicity depends on the balance of activating and inhibitory ligands expressed on their surface. Although many types of cancer cells are killed by NK cells, non-small-cell lung cancer (NSCLC) cells are relatively resistant to NK cell–mediated cytotoxicity. In this study, we showed that several NSCLC cell lines have differential sensitivity to NK cell–mediated cytotoxicity: NCI-H522 cells were highly sensitive, but A549, NCI-H23, NCI-H1915, and NCI-H1299 were resistant. Among activating ligands such as CD48, HLA-A/B/G, ICAM-1, MICA/B, and ULBPs, only CD48 rendered NCI-H522 cells susceptible to NK cell–mediated cytotoxicity, which was proved by using CD48 siRNA and neutralizing antibody. CD48-positive NCI-H522 cells established a more stable contact with NK cells than did CD48-negative A549 and CD48 siRNA cell–transfected NCI-H522 cells. Taken together, these data demonstrate that CD48-positive NSCLC cells might be susceptible to NK cell–mediated cytotoxicity, which provide information on how to stratify NSCLC patients potentially responsive to NK-cell therapy. |
doi_str_mv | 10.1007/s12272-021-01365-z |
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Although many types of cancer cells are killed by NK cells, non-small-cell lung cancer (NSCLC) cells are relatively resistant to NK cell–mediated cytotoxicity. In this study, we showed that several NSCLC cell lines have differential sensitivity to NK cell–mediated cytotoxicity: NCI-H522 cells were highly sensitive, but A549, NCI-H23, NCI-H1915, and NCI-H1299 were resistant. Among activating ligands such as CD48, HLA-A/B/G, ICAM-1, MICA/B, and ULBPs, only CD48 rendered NCI-H522 cells susceptible to NK cell–mediated cytotoxicity, which was proved by using CD48 siRNA and neutralizing antibody. CD48-positive NCI-H522 cells established a more stable contact with NK cells than did CD48-negative A549 and CD48 siRNA cell–transfected NCI-H522 cells. Taken together, these data demonstrate that CD48-positive NSCLC cells might be susceptible to NK cell–mediated cytotoxicity, which provide information on how to stratify NSCLC patients potentially responsive to NK-cell therapy.</description><identifier>ISSN: 0253-6269</identifier><identifier>EISSN: 1976-3786</identifier><identifier>DOI: 10.1007/s12272-021-01365-z</identifier><identifier>PMID: 34905179</identifier><language>eng</language><publisher>Seoul: Pharmaceutical Society of Korea</publisher><subject>Blotting, Western ; Carcinoma, Non-Small-Cell Lung - immunology ; Carcinoma, Non-Small-Cell Lung - metabolism ; CD48 Antigen - immunology ; CD48 Antigen - metabolism ; Cell Line, Tumor ; Flow Cytometry ; Humans ; Killer Cells, Natural - immunology ; Killer Cells, Natural - physiology ; Lung Neoplasms - immunology ; Lung Neoplasms - metabolism ; Medicine ; Pharmacology/Toxicology ; Pharmacy ; Polymerase Chain Reaction ; Research Article ; 약학</subject><ispartof>Archives of Pharmacal Research, 2022, 45(1), , pp.1-10</ispartof><rights>The Pharmaceutical Society of Korea 2021</rights><rights>2021. The Pharmaceutical Society of Korea.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-9a5c274c18af4c497b9ec59afe802b1d353ab60660fd4449509a3b8757a2a5463</citedby><cites>FETCH-LOGICAL-c381t-9a5c274c18af4c497b9ec59afe802b1d353ab60660fd4449509a3b8757a2a5463</cites><orcidid>0000-0001-6656-6523</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34905179$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002818389$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Eun Jae</creatorcontrib><creatorcontrib>Jun, Hye Won</creatorcontrib><creatorcontrib>Na, Ik Ho</creatorcontrib><creatorcontrib>Lee, Hong Kyung</creatorcontrib><creatorcontrib>Yun, Jieun</creatorcontrib><creatorcontrib>Kim, Hyung Sook</creatorcontrib><creatorcontrib>Kim, Youngsoo</creatorcontrib><creatorcontrib>Hong, Jin Tae</creatorcontrib><creatorcontrib>Han, Sang-Bae</creatorcontrib><title>CD48-expressing non-small-cell lung cancer cells are susceptible to natural killer cell–mediated cytotoxicity</title><title>Archives of pharmacal research</title><addtitle>Arch. Pharm. Res</addtitle><addtitle>Arch Pharm Res</addtitle><description>The susceptibility of cancer cells to natural killer (NK) cell–mediated cytotoxicity depends on the balance of activating and inhibitory ligands expressed on their surface. Although many types of cancer cells are killed by NK cells, non-small-cell lung cancer (NSCLC) cells are relatively resistant to NK cell–mediated cytotoxicity. In this study, we showed that several NSCLC cell lines have differential sensitivity to NK cell–mediated cytotoxicity: NCI-H522 cells were highly sensitive, but A549, NCI-H23, NCI-H1915, and NCI-H1299 were resistant. Among activating ligands such as CD48, HLA-A/B/G, ICAM-1, MICA/B, and ULBPs, only CD48 rendered NCI-H522 cells susceptible to NK cell–mediated cytotoxicity, which was proved by using CD48 siRNA and neutralizing antibody. CD48-positive NCI-H522 cells established a more stable contact with NK cells than did CD48-negative A549 and CD48 siRNA cell–transfected NCI-H522 cells. Taken together, these data demonstrate that CD48-positive NSCLC cells might be susceptible to NK cell–mediated cytotoxicity, which provide information on how to stratify NSCLC patients potentially responsive to NK-cell therapy.</description><subject>Blotting, Western</subject><subject>Carcinoma, Non-Small-Cell Lung - immunology</subject><subject>Carcinoma, Non-Small-Cell Lung - metabolism</subject><subject>CD48 Antigen - immunology</subject><subject>CD48 Antigen - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Flow Cytometry</subject><subject>Humans</subject><subject>Killer Cells, Natural - immunology</subject><subject>Killer Cells, Natural - physiology</subject><subject>Lung Neoplasms - immunology</subject><subject>Lung Neoplasms - metabolism</subject><subject>Medicine</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Polymerase Chain Reaction</subject><subject>Research Article</subject><subject>약학</subject><issn>0253-6269</issn><issn>1976-3786</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kc1qGzEUhUVpady0L9BF0bJZqNW_Rsvg9CcQCIRkLTSyxiiWJVeagTirvkPesE9SOeN2mdWFe79z4J4DwEeCvxCM1ddKKFUUYUoQJkwK9PgKLIhWEjHVyddggalgSFKpT8C7Wu8xbpAQb8EJ4xoLovQC5OUF75B_2BVfa0hrmHJCdWtjRM7HCOPUds4m5ws8LCq0xcM6Ved3Y-ijh2OGyY5TsRFuQoxH7s_vp61fBTv6FXT7MY_5Ibgw7t-DN4ON1X84zlNw9_3b7fInurr-cbk8v0KOdWRE2gpHFXekswN3XKteeye0HXyHaU9WTDDbSywlHlaccy2wtqzvlFCWWsElOwVns28qg9m4YLINz3OdzaaY85vbS6M1U0Lqxn6e2V3JvyZfR7MN9fCETT5P1VB5iFtqLhpKZ9SVXGvxg9mVsLVlbwg2B8rMpZhWinkuxTw20aej_9S3UP5L_rXQADYDtZ3S2hdzn6eSWj4v2f4FbT2Znw</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Park, Eun Jae</creator><creator>Jun, Hye Won</creator><creator>Na, Ik Ho</creator><creator>Lee, Hong Kyung</creator><creator>Yun, Jieun</creator><creator>Kim, Hyung Sook</creator><creator>Kim, Youngsoo</creator><creator>Hong, Jin Tae</creator><creator>Han, Sang-Bae</creator><general>Pharmaceutical Society of Korea</general><general>대한약학회</general><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>7X8</scope><scope>ACYCR</scope><orcidid>https://orcid.org/0000-0001-6656-6523</orcidid></search><sort><creationdate>2022</creationdate><title>CD48-expressing non-small-cell lung cancer cells are susceptible to natural killer cell–mediated cytotoxicity</title><author>Park, Eun Jae ; Jun, Hye Won ; Na, Ik Ho ; Lee, Hong Kyung ; Yun, Jieun ; Kim, Hyung Sook ; Kim, Youngsoo ; Hong, Jin Tae ; Han, Sang-Bae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-9a5c274c18af4c497b9ec59afe802b1d353ab60660fd4449509a3b8757a2a5463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Blotting, Western</topic><topic>Carcinoma, Non-Small-Cell Lung - immunology</topic><topic>Carcinoma, Non-Small-Cell Lung - metabolism</topic><topic>CD48 Antigen - immunology</topic><topic>CD48 Antigen - metabolism</topic><topic>Cell Line, Tumor</topic><topic>Flow Cytometry</topic><topic>Humans</topic><topic>Killer Cells, Natural - immunology</topic><topic>Killer Cells, Natural - physiology</topic><topic>Lung Neoplasms - immunology</topic><topic>Lung Neoplasms - metabolism</topic><topic>Medicine</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Polymerase Chain Reaction</topic><topic>Research Article</topic><topic>약학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Eun Jae</creatorcontrib><creatorcontrib>Jun, Hye Won</creatorcontrib><creatorcontrib>Na, Ik Ho</creatorcontrib><creatorcontrib>Lee, Hong Kyung</creatorcontrib><creatorcontrib>Yun, Jieun</creatorcontrib><creatorcontrib>Kim, Hyung Sook</creatorcontrib><creatorcontrib>Kim, Youngsoo</creatorcontrib><creatorcontrib>Hong, Jin Tae</creatorcontrib><creatorcontrib>Han, Sang-Bae</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Korean Citation Index</collection><jtitle>Archives of pharmacal research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Eun Jae</au><au>Jun, Hye Won</au><au>Na, Ik Ho</au><au>Lee, Hong Kyung</au><au>Yun, Jieun</au><au>Kim, Hyung Sook</au><au>Kim, Youngsoo</au><au>Hong, Jin Tae</au><au>Han, Sang-Bae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD48-expressing non-small-cell lung cancer cells are susceptible to natural killer cell–mediated cytotoxicity</atitle><jtitle>Archives of pharmacal research</jtitle><stitle>Arch. Pharm. Res</stitle><addtitle>Arch Pharm Res</addtitle><date>2022</date><risdate>2022</risdate><volume>45</volume><issue>1</issue><spage>1</spage><epage>10</epage><pages>1-10</pages><issn>0253-6269</issn><eissn>1976-3786</eissn><abstract>The susceptibility of cancer cells to natural killer (NK) cell–mediated cytotoxicity depends on the balance of activating and inhibitory ligands expressed on their surface. Although many types of cancer cells are killed by NK cells, non-small-cell lung cancer (NSCLC) cells are relatively resistant to NK cell–mediated cytotoxicity. In this study, we showed that several NSCLC cell lines have differential sensitivity to NK cell–mediated cytotoxicity: NCI-H522 cells were highly sensitive, but A549, NCI-H23, NCI-H1915, and NCI-H1299 were resistant. Among activating ligands such as CD48, HLA-A/B/G, ICAM-1, MICA/B, and ULBPs, only CD48 rendered NCI-H522 cells susceptible to NK cell–mediated cytotoxicity, which was proved by using CD48 siRNA and neutralizing antibody. CD48-positive NCI-H522 cells established a more stable contact with NK cells than did CD48-negative A549 and CD48 siRNA cell–transfected NCI-H522 cells. Taken together, these data demonstrate that CD48-positive NSCLC cells might be susceptible to NK cell–mediated cytotoxicity, which provide information on how to stratify NSCLC patients potentially responsive to NK-cell therapy.</abstract><cop>Seoul</cop><pub>Pharmaceutical Society of Korea</pub><pmid>34905179</pmid><doi>10.1007/s12272-021-01365-z</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-6656-6523</orcidid></addata></record> |
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subjects | Blotting, Western Carcinoma, Non-Small-Cell Lung - immunology Carcinoma, Non-Small-Cell Lung - metabolism CD48 Antigen - immunology CD48 Antigen - metabolism Cell Line, Tumor Flow Cytometry Humans Killer Cells, Natural - immunology Killer Cells, Natural - physiology Lung Neoplasms - immunology Lung Neoplasms - metabolism Medicine Pharmacology/Toxicology Pharmacy Polymerase Chain Reaction Research Article 약학 |
title | CD48-expressing non-small-cell lung cancer cells are susceptible to natural killer cell–mediated cytotoxicity |
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