Increased Soluble CD155 in the Serum of Cancer Patients

Emerging evidence suggests that DNAM-1 (CD226) play an important role in the recognition of tumor cells and their lysis by cytotoxic T lymphocytes (CTL) and NK cells. Although the DNAM-1 ligand CD155 is ubiquitously expressed in various tissues, many human tumors significantly upregulate the express...

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Published inPLoS ONE Vol. 11; no. 4; p. e0152982
Main Authors 坂東 裕子, 井口 研子, 小島 寛, 佐藤 豊実, 原 尚人, 渋谷 彰, 渋谷 和子, Yoshikawa Hiroyuki, Okumura Genki, Cho Yukiko, Hirochika Rei, Iguchi-Manaka Akiko, Bando Hiroko, Kojima Hiroshi, Sato Toyomi, Hara Hisato, Shibuya Akira, Shibuya Kazuko
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 06.04.2016
Public Library of Science (PLoS)
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ISSN1932-6203
1932-6203
DOI10.1371/journal.pone.0152982

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Summary:Emerging evidence suggests that DNAM-1 (CD226) play an important role in the recognition of tumor cells and their lysis by cytotoxic T lymphocytes (CTL) and NK cells. Although the DNAM-1 ligand CD155 is ubiquitously expressed in various tissues, many human tumors significantly upregulate the expression of CD155; DNAM-1 on CTL and NK cells may be involved in tumor immunity. However, unlike those in mice, human tissues also express soluble isoforms of CD155 (sCD155) that lack the transmembrane region. Here, we show that sCD155 levels were significantly higher in the sera of 262 patients with lung, gastrointestinal, breast, and gynecologic cancers than in sera from healthy donors. In addition, the sCD155 levels were significantly higher in patients with early stage (stages 1 and 2) gastric cancer than in healthy donors, and were significantly higher in patients with\nadvanced stage (stages 3 and 4) disease than in patients in those with early stage disease and healthy donors. Moreover, the sCD155 levels were significantly decreased after surgical resection of cancers. Thus, sCD155 level in serum may be potentially useful as a biomarker\nfor cancer development and progression.
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Conceived and designed the experiments: AIM AS KS. Performed the experiments: AIM GO RH. Analyzed the data: AIM AS KS. Contributed reagents/materials/analysis tools: AIM GO HK YC RH HB TS HY HH AS KS. Wrote the paper: AIM AS KS.
Competing Interests: The authors have declared that no competing interests exist.
Current address: Ibaraki Prefectural Central Hospital, Kasama, 309–1793, Japan
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0152982