High serum soluble CD155 level predicts poor prognosis and correlates with an immunosuppressive tumor microenvironment in hepatocellular carcinoma

Background Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies with poor prognosis. There is no research about the clinical significance of serum soluble CD155 (sCD155) level for HCC. We aim to explore the prognostic and diagnostic value of sCD155 in HCC patients undergoing cura...

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Veröffentlicht in:Journal of clinical laboratory analysis 2022-03, Vol.36 (3), p.e24259-n/a
Hauptverfasser: Jin, An‐Li, Yang, Yi‐Hui, Su, Xi, Yang, Wen‐Jing, Liu, Te, Chen, Wei, Li, Tong, Ding, Lin, Wang, Hao, Wang, Bei‐Li, Pan, Bai‐Shen, Zhou, Jian, Fan, Jia, Yang, Xin‐Rong, Guo, Wei
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container_issue 3
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container_title Journal of clinical laboratory analysis
container_volume 36
creator Jin, An‐Li
Yang, Yi‐Hui
Su, Xi
Yang, Wen‐Jing
Liu, Te
Chen, Wei
Li, Tong
Ding, Lin
Wang, Hao
Wang, Bei‐Li
Pan, Bai‐Shen
Zhou, Jian
Fan, Jia
Yang, Xin‐Rong
Guo, Wei
description Background Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies with poor prognosis. There is no research about the clinical significance of serum soluble CD155 (sCD155) level for HCC. We aim to explore the prognostic and diagnostic value of sCD155 in HCC patients undergoing curative resection. Methods Serum sCD155 level in HCC patients was determined by enzyme‐linked immunosorbent assay. The prognostic significance of sCD155 was evaluated by Cox regression and Kaplan–Meier analyses. CD155 expression and biomarkers of immune cells in HCC tissues were detected by immunohistochemistry staining. The diagnostic significance of sCD155 was evaluated using receiver operating characteristic curve. Results Serum sCD155 level was significantly increased in HCC patients and predicted poor prognosis. The prognostic value of sCD155 remained in low recurrent risk subgroups of HCC. Serum sCD155 level was positively related to CD155 expression in HCC tissues. High serum sCD155 level was associated with decreased numbers of CD8+T cells and CD56+NK cells and increased number of CD163+M2 macrophages. Serum sCD155 level had better performance in distinguishing HCC patients from healthy donors and patients with chronic liver conditions than α‐fetoprotein. Among patients with α‐fetoprotein ≤ 20 ng/ml, serum sCD155 level could differentiate HCC patients from non‐HCC patients. Conclusion Serum sCD155 level represents a promising biomarker for diagnosis and prognosis of HCC. High serum sCD155 level may reflect an immunosuppressive tumor microenvironment in HCC. Serum sCD155 level is elevated in HCC patients. High serum sCD155 level predicts poor prognosis and reflects an immunosuppressive tumor microenvironment in HCC.
doi_str_mv 10.1002/jcla.24259
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There is no research about the clinical significance of serum soluble CD155 (sCD155) level for HCC. We aim to explore the prognostic and diagnostic value of sCD155 in HCC patients undergoing curative resection. Methods Serum sCD155 level in HCC patients was determined by enzyme‐linked immunosorbent assay. The prognostic significance of sCD155 was evaluated by Cox regression and Kaplan–Meier analyses. CD155 expression and biomarkers of immune cells in HCC tissues were detected by immunohistochemistry staining. The diagnostic significance of sCD155 was evaluated using receiver operating characteristic curve. Results Serum sCD155 level was significantly increased in HCC patients and predicted poor prognosis. The prognostic value of sCD155 remained in low recurrent risk subgroups of HCC. Serum sCD155 level was positively related to CD155 expression in HCC tissues. High serum sCD155 level was associated with decreased numbers of CD8+T cells and CD56+NK cells and increased number of CD163+M2 macrophages. Serum sCD155 level had better performance in distinguishing HCC patients from healthy donors and patients with chronic liver conditions than α‐fetoprotein. Among patients with α‐fetoprotein ≤ 20 ng/ml, serum sCD155 level could differentiate HCC patients from non‐HCC patients. Conclusion Serum sCD155 level represents a promising biomarker for diagnosis and prognosis of HCC. High serum sCD155 level may reflect an immunosuppressive tumor microenvironment in HCC. Serum sCD155 level is elevated in HCC patients. High serum sCD155 level predicts poor prognosis and reflects an immunosuppressive tumor microenvironment in HCC.</description><identifier>ISSN: 0887-8013</identifier><identifier>EISSN: 1098-2825</identifier><identifier>DOI: 10.1002/jcla.24259</identifier><identifier>PMID: 35089611</identifier><language>eng</language><publisher>United States: John Wiley &amp; Sons, Inc</publisher><subject>biomarker ; Biomarkers ; Biomarkers, Tumor ; Carcinoma, Hepatocellular - pathology ; CD163 antigen ; CD56 antigen ; CD8 antigen ; CD8-Positive T-Lymphocytes - pathology ; Cholangiocarcinoma ; diagnosis ; Hepatitis ; Hepatocellular carcinoma ; Humans ; Immunohistochemistry ; immunosuppression ; Laboratories ; Liver cancer ; Liver Neoplasms - pathology ; Lymphocytes T ; Macrophages ; Medical prognosis ; Metastasis ; Patients ; Prognosis ; Risk groups ; soluble poliovirus receptor ; Standard deviation ; Statistical analysis ; Surgery ; Tumor Microenvironment ; Tumors</subject><ispartof>Journal of clinical laboratory analysis, 2022-03, Vol.36 (3), p.e24259-n/a</ispartof><rights>2022 The Authors. published by Wiley Periodicals LLC</rights><rights>2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.</rights><rights>2022. 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-c4489-ebffd507291ac380b2a585b0588724645c0b123ccbb5b5520f8478a4903340cf3</citedby><cites>FETCH-LOGICAL-c4489-ebffd507291ac380b2a585b0588724645c0b123ccbb5b5520f8478a4903340cf3</cites><orcidid>0000-0003-4406-1094 ; 0000-0001-5167-170X</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/PMC8906055/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906055/$$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/35089611$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jin, An‐Li</creatorcontrib><creatorcontrib>Yang, Yi‐Hui</creatorcontrib><creatorcontrib>Su, Xi</creatorcontrib><creatorcontrib>Yang, Wen‐Jing</creatorcontrib><creatorcontrib>Liu, Te</creatorcontrib><creatorcontrib>Chen, Wei</creatorcontrib><creatorcontrib>Li, Tong</creatorcontrib><creatorcontrib>Ding, Lin</creatorcontrib><creatorcontrib>Wang, Hao</creatorcontrib><creatorcontrib>Wang, Bei‐Li</creatorcontrib><creatorcontrib>Pan, Bai‐Shen</creatorcontrib><creatorcontrib>Zhou, Jian</creatorcontrib><creatorcontrib>Fan, Jia</creatorcontrib><creatorcontrib>Yang, Xin‐Rong</creatorcontrib><creatorcontrib>Guo, Wei</creatorcontrib><title>High serum soluble CD155 level predicts poor prognosis and correlates with an immunosuppressive tumor microenvironment in hepatocellular carcinoma</title><title>Journal of clinical laboratory analysis</title><addtitle>J Clin Lab Anal</addtitle><description>Background Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies with poor prognosis. There is no research about the clinical significance of serum soluble CD155 (sCD155) level for HCC. We aim to explore the prognostic and diagnostic value of sCD155 in HCC patients undergoing curative resection. Methods Serum sCD155 level in HCC patients was determined by enzyme‐linked immunosorbent assay. The prognostic significance of sCD155 was evaluated by Cox regression and Kaplan–Meier analyses. CD155 expression and biomarkers of immune cells in HCC tissues were detected by immunohistochemistry staining. The diagnostic significance of sCD155 was evaluated using receiver operating characteristic curve. Results Serum sCD155 level was significantly increased in HCC patients and predicted poor prognosis. The prognostic value of sCD155 remained in low recurrent risk subgroups of HCC. Serum sCD155 level was positively related to CD155 expression in HCC tissues. High serum sCD155 level was associated with decreased numbers of CD8+T cells and CD56+NK cells and increased number of CD163+M2 macrophages. Serum sCD155 level had better performance in distinguishing HCC patients from healthy donors and patients with chronic liver conditions than α‐fetoprotein. Among patients with α‐fetoprotein ≤ 20 ng/ml, serum sCD155 level could differentiate HCC patients from non‐HCC patients. Conclusion Serum sCD155 level represents a promising biomarker for diagnosis and prognosis of HCC. High serum sCD155 level may reflect an immunosuppressive tumor microenvironment in HCC. Serum sCD155 level is elevated in HCC patients. High serum sCD155 level predicts poor prognosis and reflects an immunosuppressive tumor microenvironment in HCC.</description><subject>biomarker</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>CD163 antigen</subject><subject>CD56 antigen</subject><subject>CD8 antigen</subject><subject>CD8-Positive T-Lymphocytes - pathology</subject><subject>Cholangiocarcinoma</subject><subject>diagnosis</subject><subject>Hepatitis</subject><subject>Hepatocellular carcinoma</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>immunosuppression</subject><subject>Laboratories</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - pathology</subject><subject>Lymphocytes T</subject><subject>Macrophages</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Risk groups</subject><subject>soluble poliovirus receptor</subject><subject>Standard deviation</subject><subject>Statistical analysis</subject><subject>Surgery</subject><subject>Tumor Microenvironment</subject><subject>Tumors</subject><issn>0887-8013</issn><issn>1098-2825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kc1uEzEUhS0EomlhwwMgS2wQ0pRrezzxbJCqQCkoEhtYWx7Hkzjyz2CPU_U1eGIcUipgwcp_3z06xwehFwQuCQB9u9dOXdKW8v4RWhDoRUMF5Y_RAoRYNgIIO0PnOe8BQPSke4rOGK-7jpAF-nFjtzucTSoe5-jK4AxevSecY2cOxuEpmY3Vc8ZTjKme4jbEbDNWYYN1TMk4NZuMb-28q3fYel8qUKY6l7M9GDwXXwe91SmacLApBm_CjG3AOzOpOWrjXHEqYa2StiF69Qw9GZXL5vn9eoG-XX_4urpp1l8-flpdrRvdtqJvzDCOGw5L2hOlmYCBKi74ALyGpm3Xcg0DoUzrYeAD5xRG0S6FantgrAU9sgv07qQ7lcGbja62knJyStardCejsvLvl2B3chsPUvTQAedV4PW9QIrfi8mz9DYf86hgYsmSdpRVlvC2oq_-QfexpFDjVYotqSAddJV6c6LqZ-WczPhghoA8Vi2PVctfVVf45Z_2H9Df3VaAnIBb68zdf6Tk59X66iT6ExyFt5w</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Jin, An‐Li</creator><creator>Yang, Yi‐Hui</creator><creator>Su, Xi</creator><creator>Yang, Wen‐Jing</creator><creator>Liu, Te</creator><creator>Chen, Wei</creator><creator>Li, Tong</creator><creator>Ding, Lin</creator><creator>Wang, Hao</creator><creator>Wang, Bei‐Li</creator><creator>Pan, Bai‐Shen</creator><creator>Zhou, Jian</creator><creator>Fan, Jia</creator><creator>Yang, Xin‐Rong</creator><creator>Guo, Wei</creator><general>John Wiley &amp; 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Yang, Yi‐Hui ; Su, Xi ; Yang, Wen‐Jing ; Liu, Te ; Chen, Wei ; Li, Tong ; Ding, Lin ; Wang, Hao ; Wang, Bei‐Li ; Pan, Bai‐Shen ; Zhou, Jian ; Fan, Jia ; Yang, Xin‐Rong ; Guo, Wei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4489-ebffd507291ac380b2a585b0588724645c0b123ccbb5b5520f8478a4903340cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>biomarker</topic><topic>Biomarkers</topic><topic>Biomarkers, Tumor</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>CD163 antigen</topic><topic>CD56 antigen</topic><topic>CD8 antigen</topic><topic>CD8-Positive T-Lymphocytes - pathology</topic><topic>Cholangiocarcinoma</topic><topic>diagnosis</topic><topic>Hepatitis</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>immunosuppression</topic><topic>Laboratories</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - pathology</topic><topic>Lymphocytes T</topic><topic>Macrophages</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Patients</topic><topic>Prognosis</topic><topic>Risk groups</topic><topic>soluble poliovirus receptor</topic><topic>Standard deviation</topic><topic>Statistical analysis</topic><topic>Surgery</topic><topic>Tumor Microenvironment</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jin, An‐Li</creatorcontrib><creatorcontrib>Yang, Yi‐Hui</creatorcontrib><creatorcontrib>Su, Xi</creatorcontrib><creatorcontrib>Yang, Wen‐Jing</creatorcontrib><creatorcontrib>Liu, Te</creatorcontrib><creatorcontrib>Chen, Wei</creatorcontrib><creatorcontrib>Li, Tong</creatorcontrib><creatorcontrib>Ding, Lin</creatorcontrib><creatorcontrib>Wang, Hao</creatorcontrib><creatorcontrib>Wang, Bei‐Li</creatorcontrib><creatorcontrib>Pan, Bai‐Shen</creatorcontrib><creatorcontrib>Zhou, Jian</creatorcontrib><creatorcontrib>Fan, Jia</creatorcontrib><creatorcontrib>Yang, Xin‐Rong</creatorcontrib><creatorcontrib>Guo, Wei</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 Central (Corporate)</collection><collection>Calcium &amp; 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There is no research about the clinical significance of serum soluble CD155 (sCD155) level for HCC. We aim to explore the prognostic and diagnostic value of sCD155 in HCC patients undergoing curative resection. Methods Serum sCD155 level in HCC patients was determined by enzyme‐linked immunosorbent assay. The prognostic significance of sCD155 was evaluated by Cox regression and Kaplan–Meier analyses. CD155 expression and biomarkers of immune cells in HCC tissues were detected by immunohistochemistry staining. The diagnostic significance of sCD155 was evaluated using receiver operating characteristic curve. Results Serum sCD155 level was significantly increased in HCC patients and predicted poor prognosis. The prognostic value of sCD155 remained in low recurrent risk subgroups of HCC. Serum sCD155 level was positively related to CD155 expression in HCC tissues. High serum sCD155 level was associated with decreased numbers of CD8+T cells and CD56+NK cells and increased number of CD163+M2 macrophages. Serum sCD155 level had better performance in distinguishing HCC patients from healthy donors and patients with chronic liver conditions than α‐fetoprotein. Among patients with α‐fetoprotein ≤ 20 ng/ml, serum sCD155 level could differentiate HCC patients from non‐HCC patients. Conclusion Serum sCD155 level represents a promising biomarker for diagnosis and prognosis of HCC. High serum sCD155 level may reflect an immunosuppressive tumor microenvironment in HCC. Serum sCD155 level is elevated in HCC patients. High serum sCD155 level predicts poor prognosis and reflects an immunosuppressive tumor microenvironment in HCC.</abstract><cop>United States</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>35089611</pmid><doi>10.1002/jcla.24259</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-4406-1094</orcidid><orcidid>https://orcid.org/0000-0001-5167-170X</orcidid><oa>free_for_read</oa></addata></record>
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subjects biomarker
Biomarkers
Biomarkers, Tumor
Carcinoma, Hepatocellular - pathology
CD163 antigen
CD56 antigen
CD8 antigen
CD8-Positive T-Lymphocytes - pathology
Cholangiocarcinoma
diagnosis
Hepatitis
Hepatocellular carcinoma
Humans
Immunohistochemistry
immunosuppression
Laboratories
Liver cancer
Liver Neoplasms - pathology
Lymphocytes T
Macrophages
Medical prognosis
Metastasis
Patients
Prognosis
Risk groups
soluble poliovirus receptor
Standard deviation
Statistical analysis
Surgery
Tumor Microenvironment
Tumors
title High serum soluble CD155 level predicts poor prognosis and correlates with an immunosuppressive tumor microenvironment in hepatocellular carcinoma
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