Modern Pathology advance online publication 5 February 2016; doi: 10.1038/modpathol.2016.30
Identification of microRNA expression profile related to lymph node status in women with early-stage grade 1–2 endometrial cancer
Geoffroy Canlorbe1,2,3, Zhe Wang1, Enora Laas2, Sofiane Bendifallah2,4, Mathieu Castela1, Marine Lefevre5, Nathalie Chabbert-Buffet1,2, Emile Daraï1,2,3, Selim Aractingi1, Céline Méhats6,7 and Marcos Ballester1,2,3,7
- 1INSERM, UMR S 938, University Pierre et Marie Curie, Paris, France
- 2Department of Obstetrics and Gynaecology, Tenon University Hospital, Assistance Publique des Hôpitaux de Paris (AP-HP), University Pierre and Marie Curie, et Paris, Paris, France
- 3Institut Universitaire de Cancérologie (IUC), Paris, France
- 4INSERM UMR S 707, Epidemiology, Information Systems, Modeling, University Pierre and Marie Curie, Paris, France
- 5Department of Pathology, Tenon University Hospital, University Pierre and Marie Curie, Paris, France
- 6Cochin Institute, Inserm U1016, CNRS 8104, Université Paris Descartes, Paris, France
Correspondence: Dr G Canlorbe, MD, Service de Gynécologie-Obstétrique, Hôpital Tenon, 4 rue de la Chine, 75020 Paris, France. E-mail: geoffroy.canlorbe@aphp.fr
7These authors contributed equally to this work.
Received 25 October 2015; Revised 5 December 2015; Accepted 21 December 2015
Advance online publication 5 February 2016
Advance online publication 5 February 2016
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Abstract
Conventional methods used for histologic classification and grading of endometrial cancer (EC) are not sufficient to predict lymph node metastases. microRNA signatures have recently been related to EC pathologic characteristics or prognosis. The aim of this study was to evaluate whether microRNA profiles of grade 1–2 endometrioid adenocarcinomas can be related to nodal status and used as a tool to adapt surgical staging in early-stage EC. microRNA expression was assessed in nine formalin-fixed paraffin-embedded (FFPE) EC primary tumors with positive lymph node and in 27 FFPE EC primary tumors with negative lymph node, matched for grade, stage, and lymphovascular space involvement status. A microarray analysis showed that there was more than a twofold significant difference in the expression of 12 microRNAs between the two groups. A quantitative reverse transcriptase–PCR assay was used to confirm these results: the expression levels of five microRNAs (microRNA-34c-5p, -375, -184, -34c-3p, and -34b-5p) were significantly lower in the EC primary tumor with positive lymph node compared with those with negative lymph node. A minimal P-value approach revealed that women with a microRNA-375-fold change <0.30 were more likely to have positive lymph node (n=8; 53.3%) compared with those with a microRNA-375-fold change >0.30 (n=1; 4.8%), P=0.001. Furthermore, women with a microRNA 184-fold change <0.30 were more likely to have positive lymph node (n=6; 60.0%) compared with those with a microRNA 184-fold change >0.30 (n=3; 11.5%), P=0.006. This is the first study investigating the relative expression of mature microRNA genes in early-stage grade 1–2 EC primary tumors according to the nodal status. This microRNA expression profile provides a potential basis for further study of the microRNA function in EC and could be used as a diagnostic tool for nodal status.
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