Comparison of RNA Marker Panels for Circulating Tumor Cells and Evaluation of Their Prognostic Relevance in Breast Cancer

Author:

Welsch Eva1,Schuster Eva1,Krainer Michael2ORCID,Marhold Maximilian2ORCID,Bartsch Rupert2,Fischer Michael B.34,Hermann Michael5,Hastermann Gabriele5,Uher Heidemarie5,Sliutz Gerhard56,Anker Birgit6,Zeillinger Robert1ORCID,Obermayr Eva1ORCID

Affiliation:

1. Department of Obstetrics and Gynecology, Comprehensive Cancer Center, Medical University of Vienna, 1090 Vienna, Austria

2. Department of Medicine I, Clinical Division of Oncology, Comprehensive Cancer Center, Medical University of Vienna, 1090 Vienna, Austria

3. Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, 1090 Vienna, Austria

4. Center for Biomedical Technology, Department for Biomedical Research, Danube University Krems, 3500 Krems, Austria

5. Brustgesundheitszentrum, Department of Surgery, Klinik Landstaße, Wiener Gesundheitsverbund, 1030 Vienna, Austria

6. Brustgesundheitszentrum, Department of Gynecology and Obstetrics, Klinik Landstaße, Wiener Gesundheitsverbund, 1030 Vienna, Austria

Abstract

Liquid biopsy is a promising tool for therapy monitoring of cancer patients, but a need for further research in this field exists in order to improve sensitivity, specificity, standardization and minimize costs. In our present study, we evaluated two panels of transcripts related with the presence of circulating tumor cells (CTCs) (Panel 1: CK19, EpCAM, SCGB2A2 and Panel 2: EMP2, SLC6A8, HJURP, MAL2, PPIC and CCNE2) in two cohorts of breast cancer patients (metastatic and early). A blood cell fraction possibly containing CTCs was isolated with density gradient centrifugation, followed by RNA isolation and qPCR using TaqMan® or RT-qPCR using hybridization probes. The positivity rates of the investigated panels were similar, albeit higher in metastatic (69.4% Panel 1, 75.0% Panel 2; total 86.1%) compared to early (18.9% Panel 1, 23.3% Panel 2; total 31.1%) breast cancer patients. CK19, SCGB2A2, EMP2, HJURP, MAL2, and CCNE2 individually correlated with shorter overall survival in the metastatic patient cohort. The findings highlight the additional value of Panel 2 markers, which are in contrast to CK19 and EpCAM not solely linked to an epithelial phenotype.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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