Soluble VCAM-1/soluble ICAM-1 ratio is a promising biomarker for diagnosing endometriosis

被引:76
作者
Kuessel, L. [1 ]
Wenzl, R. [1 ]
Proestling, K. [1 ]
Balendran, S. [2 ]
Pateisky, P. [1 ]
Yotova, I. [1 ]
Yerlikaya, G. [1 ,3 ]
Streubel, B. [2 ]
Husslein, H. [1 ]
机构
[1] Med Univ Vienna, Dept Gynecol & Obstet, Waehringer Guertel 18-20, A-1090 Vienna, Austria
[2] Med Univ Vienna, Dept Pathol, Waehringer Guertel 18-20, A-1090 Vienna, Austria
[3] Kings Coll Hosp London, Fetal Med Res Inst, 16-20 Windsor Walk,Denmark Hill, London SE58B, England
关键词
endometriosis; biomarker; cell adhesion molecules; VCAM-1; ICAM-1; INTERCELLULAR-ADHESION MOLECULE-1; STROMAL CELLS; EXPRESSION; WOMEN; PERITONEAL; INTEGRIN; ACTIVATION; CYTOKINES; PAXILLIN; BINDING;
D O I
10.1093/humrep/dex028
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
STUDY QUESTION: Do cell adhesion molecules play a role in endometriosis, and can they be used as a biomarker for diagnosing endometriosis? SUMMARY ANSWER: Altered expression of vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) in the endometrium and peritoneum may play a key role in endometriosis and the soluble VCAM-1/soluble ICAM-1 ratio is a promising biomarker. WHAT IS KNOWN ALREADY: Cell adhesion molecules are cell surface proteins that mediate cellular adherence, inflammatory and immune responses, and cancer-related biological processes. Altered expression of VCAM-1 and ICAM-1 in women with endometriosis has been investigated previously; however, gene expression levels in tissues and protein levels in the serum have not been investigated in the same patients. STUDY DESIGN SIZE, DURATION: We performed a prospective, longitudinal study (the Endometriosis Marker Austria) in patients who underwent a laparoscopy for benign gynecological pathology in a university-based tertiary referral center for endometriosis. From a total of 138 women who were included in the study from July 2013 through September 2014, 97 had not received hormonal treatment for at least 3 months prior to recruitment and were included in the analysis; 49 (50.5%) of these women had endometriosis, and the 48 (49.5%) who did not have endometriosis served as a control group. PARTICIPANTS/MATERIALS SETTING METHODS: During laparoscopy, tissue samples were obtained from ectopic and eutopic endometrium, and from normal pelvic peritoneum. In addition, serum samples were collected immediately before and 6-10 weeks after surgery. The mRNA levels of VCAM-1, ICAM-1 and epithelial cell adhesion molecule (EpCAM) were measured using quantitative real-time PCR, and serum protein levels of soluble VCAM-1 (sVCAM-1), ICAM-1 (sICAM-1) and EpCAM (sEpCAM) were measured using ELISA and correlated with endometriosis status. MAIN RESULTS AND THE ROLE OF CHANCE: The mRNA levels of both VCAM-1 and ICAM-1 were higher in ectopic endometriotic lesions than in eutopic endometrium (P < 0.001). Moreover, the mRNA levels of both VCAM-1 and ICAM-1 were higher in normal peritoneum samples obtained from women with endometriosis compared to those from controls (P = 0.038 and P = 0.009). The mRNA levels of VCAM-1 were also higher in the eutopic endometrium samples obtained from women with endometriosis compared to controls (P = 0.018). With respect to serum protein levels, compared to controls, the women with endometriosis had lower serum levels of sICAM-1 (P = 0.042) and higher levels of sVCAM-1 (P < 0.001). Our analysis revealed that the serum levels of sVCAM-1 were not affected by lesion entity, menstrual cycle phase or disease severity. An receiver operating characteristics curve, calculated to determine whether preoperative serum sVCAM-1 concentration can be used to predict endometriosis, found an AUC of 0.868 with 80% specificity and 84% sensitivity at a cutoff value of 370 pg/ml. This predictive performance can be further improved by calculation of the sVCAM-1/sICAM-1 ratio, leading to an AUC of 0.929 with 86.7% specificity and 90.3% sensitivity at a cutoff ratio value of 1.55. LARGE SCALE DATA: Not applicable. LIMITATIONS REASONS FOR CAUTION: The relatively small sample size in the expression analyses is a possible limitation of this study. WIDER IMPLICATIONS OF THE FINDINGS: Our findings could contribute to an improved understanding of the pathogenesis of endometriosis and the role of cell adhesion molecules. In addition, the results may lead to the development of new, non-invasive tools for diagnosing endometriosis. The ability to diagnose patients by measuring serum sVCAM-1 levels or the sVCAM-1/sICAM-1 ratio would have considerable clinical value.
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收藏
页码:770 / 779
页数:10
相关论文
共 39 条
[21]   Peripheral biomarkers of endometriosis: a systematic review [J].
May, K. E. ;
Conduit-Hulbert, S. A. ;
Villar, J. ;
Kirtley, S. ;
Kennedy, S. H. ;
Becker, C. M. .
HUMAN REPRODUCTION UPDATE, 2010, 16 (06) :651-674
[22]   The performance of CA-125 measurement in the detection of endometriosis: a meta-analysis [J].
Mol, BWJ ;
Bayram, N ;
Lijmer, JG ;
Wiegerinck, MAHM ;
Bongers, MY ;
van der Veen, F ;
Bossuyt, PMM .
FERTILITY AND STERILITY, 1998, 70 (06) :1101-1108
[23]   Adhesion molecules as diagnostic tools in tumor pathology [J].
Ohene-Abuakwa, Y ;
Pignatelli, M .
INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2000, 8 (03) :191-200
[24]   Integrins and T cell-mediated immunity [J].
Pribila, JT ;
Quale, AC ;
Mueller, KL ;
Shimizu, Y .
ANNUAL REVIEW OF IMMUNOLOGY, 2004, 22 :157-180
[25]   Enhanced epithelial to mesenchymal transition (EMT) and upregulated MYC in ectopic lesions contribute independently to endometriosis [J].
Proestling, Katharina ;
Birner, Peter ;
Gamperl, Susanne ;
Nirtl, Nadine ;
Marton, Erika ;
Yerlikaya, Guelen ;
Wenzl, Rene ;
Streubel, Berthold ;
Husslein, Heinrich .
REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, 2015, 13
[26]   Paxillin binding to the α4 integrin subunit stimulates LFA-1 (integrin αLβ2)-dependent T cell migration by augmenting the activation of focal adhesion kinase/proline-rich tyrosine kinase-2 [J].
Rose, DM ;
Liu, SC ;
Woodside, DG ;
Han, JW ;
Schlaepfer, DD ;
Ginsberg, MH .
JOURNAL OF IMMUNOLOGY, 2003, 170 (12) :5912-5918
[27]   Peritoneal endometriosis due to the menstrual dissemination of endometrial tissue into the peritoneal cavity [J].
Sampson, JA .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1927, 14 :422-469
[28]   VCAM-1 on Peritoneum and α4β1 Integrin in Endometrium and Their Implications in Endometriosis [J].
Schutt, Amy K. ;
Atkins, Kristen A. ;
Slack-Davis, Jill K. ;
Stovall, Dale W. .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 2015, 34 (01) :85-89
[29]  
Somigliana E, 1996, HUM REPROD, V11, P1190
[30]   Use of serum-soluble intercellular adhesion molecule-1 as a new marker of endometriosis [J].
Somigliana, E ;
Viganò, P ;
Candiani, M ;
Felicetta, I ;
Di Blasio, AM ;
Vignali, M .
FERTILITY AND STERILITY, 2002, 77 (05) :1028-1031