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Synaptotagmin 13 Is Highly Expressed in Estrogen Receptor-Positive Breast Cancer

Authors :
Takahiro Ichikawa
Masahiro Shibata
Takahiro Inaishi
Ikumi Soeda
Mitsuro Kanda
Masamichi Hayashi
Yuko Takano
Dai Takeuchi
Nobuyuki Tsunoda
Yasuhiro Kodera
Toyone Kikumori
Source :
Current Oncology, Vol 28, Iss 5, Pp 4080-4092 (2021)
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

Background: Accumulating evidence indicates tumor-promoting roles of synaptotagmin 13 (SYT13) in several cancers; however, no studies have investigated its expression in breast cancer (BC). This study aimed to clarify the significance of SYT13 in BC. Methods: SYT13 mRNA expression levels were evaluated in BC cell lines. Polymerase chain reaction (PCR) array analysis was conducted to determine the correlation between expression levels of SYT13 and other tumor-associated genes. Then, the association of SYT13 expression levels in the clinical BC specimens with patients’ clinicopathological factors was evaluated. These findings were subsequently validated using The Cancer Genome Atlas (TCGA) database. Results: Among 13 BC cell lines, estrogen receptor (ER)-positive cells showed higher SYT13 mRNA levels than ER-negative cells. PCR array analysis revealed positive correlations between SYT13 and several oncogenes predominantly expressed in ER-positive BC, such as estrogen receptor 1, AKT serine/threonine kinase 1, and cyclin-dependent kinases 4. In 165 patients, ER-positive specimens exhibited higher SYT13 mRNA expression levels than ER-negative specimens. The TCGA database analysis confirmed that patients with ER-positive BC expressed higher SYT13 levels than ER-negative patients. Conclusion: This study suggests that SYT13 is highly expressed in ER-positive BC cells and clinical specimens, and there is a positive association of SYT13 with the ER signaling pathways.

Details

Language :
English
ISSN :
17187729 and 11980052
Volume :
28
Issue :
5
Database :
Directory of Open Access Journals
Journal :
Current Oncology
Publication Type :
Academic Journal
Accession number :
edsdoj.3267accee694af9a7c295464eec3b90
Document Type :
article
Full Text :
https://doi.org/10.3390/curroncol28050346