Increased cytoplasmic and nuclear S100A6 expression is associated with improved prognosis in ovarian cancer

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Authors: Aruba Farooq, Evren M. Akyuz, Brandon WQ Cheah, Suha Deen, Stewart G. Martin, Mattéa J. Finelli, Sarah Storr, Alan McIntyre
Cited by: 2
References: 44

Abstract

BACKGROUND: Ovarian cancer is one of the most common gynaecological cancers affecting more than 300,000 women worldwide each year. S100 calcium-binding protein A6 (S100A6) is a member of the S100 family of calcium-binding proteins. Upon activation by calcium (Ca2+) signalling, S100A6 regulates numerous cellular processes including cell proliferation and metastasis. The role of S100A6 is well established across multiple tumour types where increased S100A6 expression contributes to tumourigenesis and worse patient outcome. However, the role of S100A6 in ovarian cancer is not well established. METHODS: The impact of cytoplasmic and nuclear S100A6 expression on overall survival and clinicopathological criteria was investigated in 462 ovarian tumours by immunohistochemistry. Additionally, S100A6 expression in an ovarian cancer cohort from The Cancer Genome Atlas (TCGA) PanCancer dataset (n = 299) was evaluated and associations with overall survival and progression-free survival were identified. RESULTS: Immunohistochemical staining revealed that high cytoplasmic expression of S100A6 was significantly associated with better overall survival (p = 0.014). Additionally, high nuclear expression was significantly associated with better overall survival (p = 0.036). In contrast, analysis of mRNA S100A6 suggests no significant association of mRNA levels for overall survival (p = 0.903) and progression free survival (p = 0.278). CONCLUSIONS: Our data provides novel insights regarding the clinical implications of S100A6 expression in ovarian cancer, providing strong rationale for functional investigations of S100A6 in ovarian cancer.

Fields of Study & Subjects

S100 Proteins and Annexins Connective Tissue Growth Factor Research Mechanisms of cancer metastasis

Publication details

Journal / source
BMC Cancer
Publisher
Springer Science and Business Media LLC
Volume
26
Issue
1
Publication date
11 February 2026
Language
EN