The 3q Oncogene SEC62 Predicts Response to Neoadjuvant Chemotherapy and Regulates Tumor Cell Migration in Triple Negative Breast Cancer

Author:

Radosa Julia C.1,Kasoha Mariz1ORCID,Doerk Merle1,Cullmann Annika1,Kaya Askin C.1,Linxweiler Maximilian2ORCID,Radosa Marc P.13,Takacs Zoltan1,Tirincsi Andrea4,Lang Sven4,Jung Martin4ORCID,Puppe Julian5ORCID,Linxweiler Barbara1,Wagner Mathias6,Bohle Rainer M.6,Solomayer Erich-Franz1,Zimmermann Julia S. M.1ORCID

Affiliation:

1. Department of Gynecology, Obstetrics and Reproductive Medicine, Saarland University Hospital, D-66421 Homburg, Germany

2. Department of Otorhinolaryngology, Head and Neck Surgery, Saarland University Hospital, D-66421 Homburg, Germany

3. Department of Gynecology and Obstetrics, Klinikum Bremen Nord, D-28755 Bremen, Germany

4. Medical Biochemistry and Molecular Biology, Saarland University, D-66421 Homburg, Germany

5. Department of Gynecology, University Hospital Cologne, D-50931 Cologne, Germany

6. Department of Pathology, Saarland University Hospital, D-66421 Homburg, Germany

Abstract

In the absence of targeted treatment options, neoadjuvant chemotherapy (NACT) is applied widely for triple-negative breast cancer (TNBC). Response to NACT is an important parameter predictive of oncological outcomes (progression-free and overall survival). An approach to the evaluation of predictive markers enabling therapy individualization is the identification of tumor driver genetic mutations. This study was conducted to investigate the role of SEC62, harbored at 3q26 and identified as a driver of breast cancer pathogenesis, in TNBC. We analyzed SEC62 expression in The Cancer Genome Atlas database, and immunohistologically investigated SEC62 expression in pre- and post-NACT tissue samples from 64 patients with TNBC treated at the Department of Gynecology and Obstetrics/Saarland University Hospital/Homburg between January 2010 and December 2018 and compared the effect of SEC62 on tumor cell migration and proliferation in functional assays. SEC62 expression dynamics correlated positively with the response to NACT (p ≤ 0.01) and oncological outcomes (p ≤ 0.01). SEC62 expression stimulated tumor cell migration (p ≤ 0.01). The study findings indicate that SEC62 is overexpressed in TNBC and serves as a predictive marker for the response to NACT, a prognostic marker for oncological outcomes, and a migration-stimulating oncogene in TNBC.

Funder

HOMFOR

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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