The Expression of VISTA on CD4+ T Cells Associate with Poor Prognosis and Immune Status in Non-small Cell Lung Cancer Patients
Besides the two main histologic types of papillary thyroid carcinoma (PTC), the classical PTC (CL-PTC) and the follicular variant PTC (FV-PTC), several other variants are described. The encapsulated FV-PTC variant was recently reclassified as noninvasive follicular thyroid neoplasm with papillary-li...
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Veröffentlicht in: | Biomolecules & biomedicine 2022-02, Vol.22 (5) |
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description | Besides the two main histologic types of papillary thyroid carcinoma (PTC), the classical PTC (CL-PTC) and the follicular variant PTC (FV-PTC), several other variants are described. The encapsulated FV-PTC variant was recently reclassified as noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) due to its similarities to benign lesions. Specific molecular signatures, however, are still unavailable. It is well known that improper DNA repair of dysfunctional telomeres may cause telomere-related genome instability. The mechanisms involved in the damaged telomere repair processing may lead to detrimental outcomes, altering the three-dimensional (3D) nuclear telomere and genome organization in cancer cells. This pilot study aimed to evaluate whether a specific 3D nuclear telomere architecture might characterize NIFTP, potentially distinguishing it from other PTC histologic variants. Our findings demonstrate that 3D telomere profiles of CL-PTC and FV-PTC were different from NIFTP and that NIFTP more closely resembles follicular thyroid adenoma (FTA). NIFTP has longer telomeres than CL-PTC and FV-PTC samples, and the telomere length of NIFTP overlaps with that of the FTA histotype. In contrast, there was no association between BRAF expression and telomere length in all tested samples. These preliminary findings reinforce the view that NIFTP is closer to non-malignant thyroid nodules and confirm that PTC features short telomeres. |
doi_str_mv | 10.17305/bjbms.2021.6531 |
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The encapsulated FV-PTC variant was recently reclassified as noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) due to its similarities to benign lesions. Specific molecular signatures, however, are still unavailable. It is well known that improper DNA repair of dysfunctional telomeres may cause telomere-related genome instability. The mechanisms involved in the damaged telomere repair processing may lead to detrimental outcomes, altering the three-dimensional (3D) nuclear telomere and genome organization in cancer cells. This pilot study aimed to evaluate whether a specific 3D nuclear telomere architecture might characterize NIFTP, potentially distinguishing it from other PTC histologic variants. Our findings demonstrate that 3D telomere profiles of CL-PTC and FV-PTC were different from NIFTP and that NIFTP more closely resembles follicular thyroid adenoma (FTA). NIFTP has longer telomeres than CL-PTC and FV-PTC samples, and the telomere length of NIFTP overlaps with that of the FTA histotype. In contrast, there was no association between BRAF expression and telomere length in all tested samples. These preliminary findings reinforce the view that NIFTP is closer to non-malignant thyroid nodules and confirm that PTC features short telomeres.</description><identifier>ISSN: 1512-8601</identifier><identifier>ISSN: 2831-0896</identifier><identifier>EISSN: 1840-4812</identifier><identifier>EISSN: 2831-090X</identifier><identifier>DOI: 10.17305/bjbms.2021.6531</identifier><identifier>PMID: 35122478</identifier><language>eng</language><publisher>Bosnia and Herzegovina: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina</publisher><subject>CD4 T cells ; Immune status ; Non-small cell lung cancer ; Prognosis ; VISTA</subject><ispartof>Biomolecules & biomedicine, 2022-02, Vol.22 (5)</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1778-89dc9f6b056074d6418cf4062de960d23ddb2dedf7dd513719a18d62a2d744103</citedby><orcidid>0000-0002-7430-5574 ; 0000-0002-9916-5686 ; 0000-0003-4751-7253 ; 0000-0003-2464-6773 ; 0000-0003-0526-1843 ; 0000-0002-8367-5892 ; 0000-0002-9084-2126 ; 0000-0001-5142-8611 ; 0000-0003-0780-7598 ; 0000-0001-8459-0439</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35122478$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ma, Shengyao</creatorcontrib><creatorcontrib>Qin, Liya</creatorcontrib><creatorcontrib>Wang, Xinling</creatorcontrib><creatorcontrib>Wang, Weiyu</creatorcontrib><creatorcontrib>Li, Jinfeng</creatorcontrib><creatorcontrib>Wang, Huaijie</creatorcontrib><creatorcontrib>Li, Hanyue</creatorcontrib><creatorcontrib>Cai, Xiaoshan</creatorcontrib><creatorcontrib>Yang, Yang</creatorcontrib><creatorcontrib>Qu, Meihua</creatorcontrib><title>The Expression of VISTA on CD4+ T Cells Associate with Poor Prognosis and Immune Status in Non-small Cell Lung Cancer Patients</title><title>Biomolecules & biomedicine</title><addtitle>Bosn J Basic Med Sci</addtitle><description>Besides the two main histologic types of papillary thyroid carcinoma (PTC), the classical PTC (CL-PTC) and the follicular variant PTC (FV-PTC), several other variants are described. The encapsulated FV-PTC variant was recently reclassified as noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) due to its similarities to benign lesions. Specific molecular signatures, however, are still unavailable. It is well known that improper DNA repair of dysfunctional telomeres may cause telomere-related genome instability. The mechanisms involved in the damaged telomere repair processing may lead to detrimental outcomes, altering the three-dimensional (3D) nuclear telomere and genome organization in cancer cells. This pilot study aimed to evaluate whether a specific 3D nuclear telomere architecture might characterize NIFTP, potentially distinguishing it from other PTC histologic variants. Our findings demonstrate that 3D telomere profiles of CL-PTC and FV-PTC were different from NIFTP and that NIFTP more closely resembles follicular thyroid adenoma (FTA). NIFTP has longer telomeres than CL-PTC and FV-PTC samples, and the telomere length of NIFTP overlaps with that of the FTA histotype. In contrast, there was no association between BRAF expression and telomere length in all tested samples. These preliminary findings reinforce the view that NIFTP is closer to non-malignant thyroid nodules and confirm that PTC features short telomeres.</description><subject>CD4 T cells</subject><subject>Immune status</subject><subject>Non-small cell lung cancer</subject><subject>Prognosis</subject><subject>VISTA</subject><issn>1512-8601</issn><issn>2831-0896</issn><issn>1840-4812</issn><issn>2831-090X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNo9kU1vEzEQhi1UREvhzqnyvdrg8fprj9E2QKQIKjVwtby2N3W0a0f2Ri0XfjvbBHqaVzN6nzk8CH0CsgBZE_6523djWVBCYSF4DW_QFShGKqaAXsyZA62UIHCJ3peyJ0Q0tWLv0GU9HyiT6gr92T56vHo-ZF9KSBGnHv9aP2yXeM7tHbvFW9z6YSh4WUqywUweP4XpEd-nlPF9TruYSijYRIfX43iMHj9MZjoWHCL-nmJVRjMMJwTeHOMOtyZaPzfNFHycygf0tjdD8R__zWv088tq236rNj--rtvlprIgpapU42zTi45wQSRzgoGyPSOCOt8I4mjtXDdn10vnONQSGgPKCWqok4wBqa_R-sx1yez1IYfR5N86maBPi5R32uQp2MFry4F3TlnueM9U3yjjiSeGq07y-QHMLHJm2ZxKyb5_5QHRJy36pEW_aNEvWubKzblyOHajd6-F_x7qv4joiHw</recordid><startdate>20220205</startdate><enddate>20220205</enddate><creator>Ma, Shengyao</creator><creator>Qin, Liya</creator><creator>Wang, Xinling</creator><creator>Wang, Weiyu</creator><creator>Li, Jinfeng</creator><creator>Wang, Huaijie</creator><creator>Li, Hanyue</creator><creator>Cai, Xiaoshan</creator><creator>Yang, Yang</creator><creator>Qu, Meihua</creator><general>Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-7430-5574</orcidid><orcidid>https://orcid.org/0000-0002-9916-5686</orcidid><orcidid>https://orcid.org/0000-0003-4751-7253</orcidid><orcidid>https://orcid.org/0000-0003-2464-6773</orcidid><orcidid>https://orcid.org/0000-0003-0526-1843</orcidid><orcidid>https://orcid.org/0000-0002-8367-5892</orcidid><orcidid>https://orcid.org/0000-0002-9084-2126</orcidid><orcidid>https://orcid.org/0000-0001-5142-8611</orcidid><orcidid>https://orcid.org/0000-0003-0780-7598</orcidid><orcidid>https://orcid.org/0000-0001-8459-0439</orcidid></search><sort><creationdate>20220205</creationdate><title>The Expression of VISTA on CD4+ T Cells Associate with Poor Prognosis and Immune Status in Non-small Cell Lung Cancer Patients</title><author>Ma, Shengyao ; Qin, Liya ; Wang, Xinling ; Wang, Weiyu ; Li, Jinfeng ; Wang, Huaijie ; Li, Hanyue ; Cai, Xiaoshan ; Yang, Yang ; Qu, Meihua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1778-89dc9f6b056074d6418cf4062de960d23ddb2dedf7dd513719a18d62a2d744103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>CD4 T cells</topic><topic>Immune status</topic><topic>Non-small cell lung cancer</topic><topic>Prognosis</topic><topic>VISTA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma, Shengyao</creatorcontrib><creatorcontrib>Qin, Liya</creatorcontrib><creatorcontrib>Wang, Xinling</creatorcontrib><creatorcontrib>Wang, Weiyu</creatorcontrib><creatorcontrib>Li, Jinfeng</creatorcontrib><creatorcontrib>Wang, Huaijie</creatorcontrib><creatorcontrib>Li, Hanyue</creatorcontrib><creatorcontrib>Cai, Xiaoshan</creatorcontrib><creatorcontrib>Yang, Yang</creatorcontrib><creatorcontrib>Qu, Meihua</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Biomolecules & biomedicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ma, Shengyao</au><au>Qin, Liya</au><au>Wang, Xinling</au><au>Wang, Weiyu</au><au>Li, Jinfeng</au><au>Wang, Huaijie</au><au>Li, Hanyue</au><au>Cai, Xiaoshan</au><au>Yang, Yang</au><au>Qu, Meihua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Expression of VISTA on CD4+ T Cells Associate with Poor Prognosis and Immune Status in Non-small Cell Lung Cancer Patients</atitle><jtitle>Biomolecules & biomedicine</jtitle><addtitle>Bosn J Basic Med Sci</addtitle><date>2022-02-05</date><risdate>2022</risdate><volume>22</volume><issue>5</issue><issn>1512-8601</issn><issn>2831-0896</issn><eissn>1840-4812</eissn><eissn>2831-090X</eissn><abstract>Besides the two main histologic types of papillary thyroid carcinoma (PTC), the classical PTC (CL-PTC) and the follicular variant PTC (FV-PTC), several other variants are described. The encapsulated FV-PTC variant was recently reclassified as noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) due to its similarities to benign lesions. Specific molecular signatures, however, are still unavailable. It is well known that improper DNA repair of dysfunctional telomeres may cause telomere-related genome instability. The mechanisms involved in the damaged telomere repair processing may lead to detrimental outcomes, altering the three-dimensional (3D) nuclear telomere and genome organization in cancer cells. This pilot study aimed to evaluate whether a specific 3D nuclear telomere architecture might characterize NIFTP, potentially distinguishing it from other PTC histologic variants. Our findings demonstrate that 3D telomere profiles of CL-PTC and FV-PTC were different from NIFTP and that NIFTP more closely resembles follicular thyroid adenoma (FTA). NIFTP has longer telomeres than CL-PTC and FV-PTC samples, and the telomere length of NIFTP overlaps with that of the FTA histotype. In contrast, there was no association between BRAF expression and telomere length in all tested samples. 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subjects | CD4 T cells Immune status Non-small cell lung cancer Prognosis VISTA |
title | The Expression of VISTA on CD4+ T Cells Associate with Poor Prognosis and Immune Status in Non-small Cell Lung Cancer Patients |
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