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T Lymphocyte Infiltration in Association with IDO1 Expression in Resected Lung Adenocarcinoma and Normal Adjacent Lung Tissues
Background. Indoleamine 2,3-dioxygenase 1 (IDO1) catalyzes the first step of tryptophan catabolism in the kynurenine (Kyn) pathway. IDO1 downregulates natural killer cell receptors, and by mechanism, tumor cells escape immune surveillance. Methods. IDO1 protein and mRNA were assessed by immunohistoc...
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Published in: | BioMed research international 2022-02, Vol.2022, p.2381018-9 |
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description | Background. Indoleamine 2,3-dioxygenase 1 (IDO1) catalyzes the first step of tryptophan catabolism in the kynurenine (Kyn) pathway. IDO1 downregulates natural killer cell receptors, and by mechanism, tumor cells escape immune surveillance. Methods. IDO1 protein and mRNA were assessed by immunohistochemistry, immunoblotting, and PCR in the 68 resected lung adenocarcinomas at stages I–III as well as adjacent normal lung tissues. Infiltration of CD3, CD8, and CD4 lymphocytes in the tumor and adjacent normal lung tissues was assessed by immunohistochemical staining. Results. IDO1 protein and mRNA were detected in various stages of lung adenocarcinoma with highest expression at stage III. In contrast, biomarkers of T cell subset, CD3, CD4, and CD8, were highly expressed in the normal lung tissues and stage I adenocarcinoma tissues but significantly reduced in the stage II and III tumor tissues. Conclusions. The current study demonstrated that the higher level of IDO1 expression in the lung adenocarcinoma was, the less infiltration of T lymphocytes was found in the tumors. Findings of this study indicated that IDO1 may contribute to the reduction of T lymphocyte infiltration into the lung adenocarcinoma. |
doi_str_mv | 10.1155/2022/2381018 |
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Indoleamine 2,3-dioxygenase 1 (IDO1) catalyzes the first step of tryptophan catabolism in the kynurenine (Kyn) pathway. IDO1 downregulates natural killer cell receptors, and by mechanism, tumor cells escape immune surveillance. Methods. IDO1 protein and mRNA were assessed by immunohistochemistry, immunoblotting, and PCR in the 68 resected lung adenocarcinomas at stages I–III as well as adjacent normal lung tissues. Infiltration of CD3, CD8, and CD4 lymphocytes in the tumor and adjacent normal lung tissues was assessed by immunohistochemical staining. Results. IDO1 protein and mRNA were detected in various stages of lung adenocarcinoma with highest expression at stage III. In contrast, biomarkers of T cell subset, CD3, CD4, and CD8, were highly expressed in the normal lung tissues and stage I adenocarcinoma tissues but significantly reduced in the stage II and III tumor tissues. Conclusions. The current study demonstrated that the higher level of IDO1 expression in the lung adenocarcinoma was, the less infiltration of T lymphocytes was found in the tumors. Findings of this study indicated that IDO1 may contribute to the reduction of T lymphocyte infiltration into the lung adenocarcinoma.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2022/2381018</identifier><identifier>PMID: 35187162</identifier><language>eng</language><publisher>United States: Hindawi</publisher><subject>Adenocarcinoma ; Adenocarcinoma of Lung - immunology ; Adenocarcinoma of Lung - pathology ; Adenocarcinoma of Lung - surgery ; Adult ; Aged ; Antibodies ; Apoptosis ; Biomarkers ; Catabolism ; CD3 antigen ; CD4 antigen ; CD4-Positive T-Lymphocytes - immunology ; CD8 antigen ; Chemotherapy ; Development and progression ; Female ; Gene expression ; Genetic aspects ; Health aspects ; Histology ; Humans ; Immunoblotting ; Immunohistochemistry ; Immunosurveillance ; Immunotherapy ; Indoleamine-Pyrrole 2,3,-Dioxygenase - immunology ; Infiltration ; Kinases ; Lung cancer ; Lungs ; Lymphocytes ; Lymphocytes T ; Male ; Metastases ; Middle Aged ; mRNA ; Mutation ; Natural killer cells ; Neoplasm Staging ; Oxidoreductases ; Proteins ; RNA, Messenger - metabolism ; Statistical analysis ; T cells ; Thoracic surgery ; Tissues ; Tryptophan ; Tryptophan 2,3-dioxygenase ; Tryptophan metabolism ; Tumor cells ; Tumors</subject><ispartof>BioMed research international, 2022-02, Vol.2022, p.2381018-9</ispartof><rights>Copyright © 2022 Xiaoling Zhao et al.</rights><rights>COPYRIGHT 2022 John Wiley & Sons, Inc.</rights><rights>Copyright © 2022 Xiaoling Zhao et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2022 Xiaoling Zhao et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-63e55b74a727b5b4461a7e5ab0fa63187c23874735813bd486feadcb51bba9b53</citedby><cites>FETCH-LOGICAL-c476t-63e55b74a727b5b4461a7e5ab0fa63187c23874735813bd486feadcb51bba9b53</cites><orcidid>0000-0001-8905-9698 ; 0000-0002-7512-6666 ; 0000-0002-9864-1740 ; 0000-0002-2608-6354 ; 0000-0002-8249-1653 ; 0000-0003-0198-362X ; 0000-0002-8413-5492 ; 0000-0002-9864-0561 ; 0000-0001-5678-6127 ; 0000-0001-8121-5895</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2630681839/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2630681839?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,25753,27924,27925,37012,37013,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35187162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Aga, Syed Sameer</contributor><contributor>Syed Sameer Aga</contributor><creatorcontrib>Zhao, Xiaoling</creatorcontrib><creatorcontrib>Li, Yaran</creatorcontrib><creatorcontrib>Yang, Xu</creatorcontrib><creatorcontrib>Zhang, Xiaochong</creatorcontrib><creatorcontrib>Xie, Jing</creatorcontrib><creatorcontrib>Li, Shaoteng</creatorcontrib><creatorcontrib>Liu, Hongzhen</creatorcontrib><creatorcontrib>Guo, Jun</creatorcontrib><creatorcontrib>He, Lili</creatorcontrib><creatorcontrib>Chen, Wei</creatorcontrib><creatorcontrib>Liu, Dengxiang</creatorcontrib><title>T Lymphocyte Infiltration in Association with IDO1 Expression in Resected Lung Adenocarcinoma and Normal Adjacent Lung Tissues</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Background. Indoleamine 2,3-dioxygenase 1 (IDO1) catalyzes the first step of tryptophan catabolism in the kynurenine (Kyn) pathway. IDO1 downregulates natural killer cell receptors, and by mechanism, tumor cells escape immune surveillance. Methods. IDO1 protein and mRNA were assessed by immunohistochemistry, immunoblotting, and PCR in the 68 resected lung adenocarcinomas at stages I–III as well as adjacent normal lung tissues. Infiltration of CD3, CD8, and CD4 lymphocytes in the tumor and adjacent normal lung tissues was assessed by immunohistochemical staining. Results. IDO1 protein and mRNA were detected in various stages of lung adenocarcinoma with highest expression at stage III. In contrast, biomarkers of T cell subset, CD3, CD4, and CD8, were highly expressed in the normal lung tissues and stage I adenocarcinoma tissues but significantly reduced in the stage II and III tumor tissues. Conclusions. The current study demonstrated that the higher level of IDO1 expression in the lung adenocarcinoma was, the less infiltration of T lymphocytes was found in the tumors. Findings of this study indicated that IDO1 may contribute to the reduction of T lymphocyte infiltration into the lung adenocarcinoma.</description><subject>Adenocarcinoma</subject><subject>Adenocarcinoma of Lung - immunology</subject><subject>Adenocarcinoma of Lung - pathology</subject><subject>Adenocarcinoma of Lung - surgery</subject><subject>Adult</subject><subject>Aged</subject><subject>Antibodies</subject><subject>Apoptosis</subject><subject>Biomarkers</subject><subject>Catabolism</subject><subject>CD3 antigen</subject><subject>CD4 antigen</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD8 antigen</subject><subject>Chemotherapy</subject><subject>Development and progression</subject><subject>Female</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Histology</subject><subject>Humans</subject><subject>Immunoblotting</subject><subject>Immunohistochemistry</subject><subject>Immunosurveillance</subject><subject>Immunotherapy</subject><subject>Indoleamine-Pyrrole 2,3,-Dioxygenase - immunology</subject><subject>Infiltration</subject><subject>Kinases</subject><subject>Lung cancer</subject><subject>Lungs</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Metastases</subject><subject>Middle Aged</subject><subject>mRNA</subject><subject>Mutation</subject><subject>Natural killer cells</subject><subject>Neoplasm Staging</subject><subject>Oxidoreductases</subject><subject>Proteins</subject><subject>RNA, Messenger - metabolism</subject><subject>Statistical analysis</subject><subject>T cells</subject><subject>Thoracic surgery</subject><subject>Tissues</subject><subject>Tryptophan</subject><subject>Tryptophan 2,3-dioxygenase</subject><subject>Tryptophan metabolism</subject><subject>Tumor cells</subject><subject>Tumors</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9ks2LEzEYxoMo7lL35lkCXgStO_lOL0JZVy0UF6SeQ5LJtCkzSU1mdu3Fv90MU8vqwVyS8P548jx5XwBeouo9Qoxd4wrja0wkqpB8Ai4xQXTOEUVPz2dCLsBVzvuqLIl4teDPwQVhSArE8SX4tYHrY3fYRXvsHVyFxrd90r2PAfoAlzlH66frg-93cPXxDsHbn4fkcj4x31x2tnc1XA9hC5e1C9HqZH2InYY61PBrTJ1uS2WvrQv9xG18zoPLL8CzRrfZXZ32Gfj-6XZz82W-vvu8ulmu55YK3s85cYwZQbXAwjBDKUdaOKZN1WhOShZb_kBQQZhExNRU8sbp2hqGjNELw8gMfJh0D4PpXD36SLpVh-Q7nY4qaq_-rgS_U9t4r6RkREhaBN6cBFL8UYz3qvPZurbVwcUhK1xscCQ5WhT09T_oPg4plHgjVXGJJHlEbXXrlA9NLO_aUVQt-UJwisfezcC7ibIp5pxcc7aMKjVOgBonQJ0moOCvHsc8w3_6XYC3E7DzodYP_v9yvwGEqbfg</recordid><startdate>20220210</startdate><enddate>20220210</enddate><creator>Zhao, Xiaoling</creator><creator>Li, Yaran</creator><creator>Yang, Xu</creator><creator>Zhang, Xiaochong</creator><creator>Xie, Jing</creator><creator>Li, Shaoteng</creator><creator>Liu, Hongzhen</creator><creator>Guo, Jun</creator><creator>He, Lili</creator><creator>Chen, Wei</creator><creator>Liu, Dengxiang</creator><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</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>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8905-9698</orcidid><orcidid>https://orcid.org/0000-0002-7512-6666</orcidid><orcidid>https://orcid.org/0000-0002-9864-1740</orcidid><orcidid>https://orcid.org/0000-0002-2608-6354</orcidid><orcidid>https://orcid.org/0000-0002-8249-1653</orcidid><orcidid>https://orcid.org/0000-0003-0198-362X</orcidid><orcidid>https://orcid.org/0000-0002-8413-5492</orcidid><orcidid>https://orcid.org/0000-0002-9864-0561</orcidid><orcidid>https://orcid.org/0000-0001-5678-6127</orcidid><orcidid>https://orcid.org/0000-0001-8121-5895</orcidid></search><sort><creationdate>20220210</creationdate><title>T Lymphocyte Infiltration in Association with IDO1 Expression in Resected Lung Adenocarcinoma and Normal Adjacent Lung Tissues</title><author>Zhao, Xiaoling ; Li, Yaran ; Yang, Xu ; Zhang, Xiaochong ; Xie, Jing ; Li, Shaoteng ; Liu, Hongzhen ; Guo, Jun ; He, Lili ; Chen, Wei ; Liu, Dengxiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-63e55b74a727b5b4461a7e5ab0fa63187c23874735813bd486feadcb51bba9b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adenocarcinoma</topic><topic>Adenocarcinoma of Lung - immunology</topic><topic>Adenocarcinoma of Lung - pathology</topic><topic>Adenocarcinoma of Lung - surgery</topic><topic>Adult</topic><topic>Aged</topic><topic>Antibodies</topic><topic>Apoptosis</topic><topic>Biomarkers</topic><topic>Catabolism</topic><topic>CD3 antigen</topic><topic>CD4 antigen</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD8 antigen</topic><topic>Chemotherapy</topic><topic>Development and progression</topic><topic>Female</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Histology</topic><topic>Humans</topic><topic>Immunoblotting</topic><topic>Immunohistochemistry</topic><topic>Immunosurveillance</topic><topic>Immunotherapy</topic><topic>Indoleamine-Pyrrole 2,3,-Dioxygenase - immunology</topic><topic>Infiltration</topic><topic>Kinases</topic><topic>Lung cancer</topic><topic>Lungs</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Metastases</topic><topic>Middle Aged</topic><topic>mRNA</topic><topic>Mutation</topic><topic>Natural killer cells</topic><topic>Neoplasm Staging</topic><topic>Oxidoreductases</topic><topic>Proteins</topic><topic>RNA, Messenger - metabolism</topic><topic>Statistical analysis</topic><topic>T cells</topic><topic>Thoracic surgery</topic><topic>Tissues</topic><topic>Tryptophan</topic><topic>Tryptophan 2,3-dioxygenase</topic><topic>Tryptophan metabolism</topic><topic>Tumor cells</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Xiaoling</creatorcontrib><creatorcontrib>Li, Yaran</creatorcontrib><creatorcontrib>Yang, Xu</creatorcontrib><creatorcontrib>Zhang, Xiaochong</creatorcontrib><creatorcontrib>Xie, Jing</creatorcontrib><creatorcontrib>Li, Shaoteng</creatorcontrib><creatorcontrib>Liu, Hongzhen</creatorcontrib><creatorcontrib>Guo, Jun</creatorcontrib><creatorcontrib>He, Lili</creatorcontrib><creatorcontrib>Chen, Wei</creatorcontrib><creatorcontrib>Liu, Dengxiang</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing 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 Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</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>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BioMed research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Xiaoling</au><au>Li, Yaran</au><au>Yang, Xu</au><au>Zhang, Xiaochong</au><au>Xie, Jing</au><au>Li, Shaoteng</au><au>Liu, Hongzhen</au><au>Guo, Jun</au><au>He, Lili</au><au>Chen, Wei</au><au>Liu, Dengxiang</au><au>Aga, Syed Sameer</au><au>Syed Sameer Aga</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>T Lymphocyte Infiltration in Association with IDO1 Expression in Resected Lung Adenocarcinoma and Normal Adjacent Lung Tissues</atitle><jtitle>BioMed research international</jtitle><addtitle>Biomed Res Int</addtitle><date>2022-02-10</date><risdate>2022</risdate><volume>2022</volume><spage>2381018</spage><epage>9</epage><pages>2381018-9</pages><issn>2314-6133</issn><eissn>2314-6141</eissn><abstract>Background. Indoleamine 2,3-dioxygenase 1 (IDO1) catalyzes the first step of tryptophan catabolism in the kynurenine (Kyn) pathway. IDO1 downregulates natural killer cell receptors, and by mechanism, tumor cells escape immune surveillance. Methods. IDO1 protein and mRNA were assessed by immunohistochemistry, immunoblotting, and PCR in the 68 resected lung adenocarcinomas at stages I–III as well as adjacent normal lung tissues. Infiltration of CD3, CD8, and CD4 lymphocytes in the tumor and adjacent normal lung tissues was assessed by immunohistochemical staining. Results. IDO1 protein and mRNA were detected in various stages of lung adenocarcinoma with highest expression at stage III. In contrast, biomarkers of T cell subset, CD3, CD4, and CD8, were highly expressed in the normal lung tissues and stage I adenocarcinoma tissues but significantly reduced in the stage II and III tumor tissues. Conclusions. The current study demonstrated that the higher level of IDO1 expression in the lung adenocarcinoma was, the less infiltration of T lymphocytes was found in the tumors. Findings of this study indicated that IDO1 may contribute to the reduction of T lymphocyte infiltration into the lung adenocarcinoma.</abstract><cop>United States</cop><pub>Hindawi</pub><pmid>35187162</pmid><doi>10.1155/2022/2381018</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8905-9698</orcidid><orcidid>https://orcid.org/0000-0002-7512-6666</orcidid><orcidid>https://orcid.org/0000-0002-9864-1740</orcidid><orcidid>https://orcid.org/0000-0002-2608-6354</orcidid><orcidid>https://orcid.org/0000-0002-8249-1653</orcidid><orcidid>https://orcid.org/0000-0003-0198-362X</orcidid><orcidid>https://orcid.org/0000-0002-8413-5492</orcidid><orcidid>https://orcid.org/0000-0002-9864-0561</orcidid><orcidid>https://orcid.org/0000-0001-5678-6127</orcidid><orcidid>https://orcid.org/0000-0001-8121-5895</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Adenocarcinoma of Lung - immunology Adenocarcinoma of Lung - pathology Adenocarcinoma of Lung - surgery Adult Aged Antibodies Apoptosis Biomarkers Catabolism CD3 antigen CD4 antigen CD4-Positive T-Lymphocytes - immunology CD8 antigen Chemotherapy Development and progression Female Gene expression Genetic aspects Health aspects Histology Humans Immunoblotting Immunohistochemistry Immunosurveillance Immunotherapy Indoleamine-Pyrrole 2,3,-Dioxygenase - immunology Infiltration Kinases Lung cancer Lungs Lymphocytes Lymphocytes T Male Metastases Middle Aged mRNA Mutation Natural killer cells Neoplasm Staging Oxidoreductases Proteins RNA, Messenger - metabolism Statistical analysis T cells Thoracic surgery Tissues Tryptophan Tryptophan 2,3-dioxygenase Tryptophan metabolism Tumor cells Tumors |
title | T Lymphocyte Infiltration in Association with IDO1 Expression in Resected Lung Adenocarcinoma and Normal Adjacent Lung Tissues |
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