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Immunohistochemistry for thymidine kinase-1 (Tk1): A potential tool for the prognostic stratification of breast cancer patients

Authors :
Paola Cinacchi
Anna Szumera-Ciećkiewicz
Beatrice Fuochi
Mario Miccoli
Cristian Scatena
Paola Ferrari
Andrea Fontana
Antonio Giuseppe Naccarato
Rosa Scarpitta
Giuseppe Nicolò Fanelli
Katia De Ieso
Source :
Journal of Clinical Medicine, Volume 10, Issue 22, Journal of Clinical Medicine, Vol 10, Iss 5416, p 5416 (2021)
Publication Year :
2021

Abstract

Breast cancer (BC) is the most frequent non-cutaneous malignancy in women. Histological grade, expression of estrogen and progesterone receptors (ER and PgR), overexpression/amplification of the human epidermal growth factor receptor 2 (HER2) oncogene, and proliferative activity measured with ki-67 provide important information on the biological features of BC and guide treatment choices. However, a biomarker that allows a more accurate prognostic stratification is still lacking. Thymidine kinase-1 (TK1), a ubiquitous enzyme involved in the pyrimidine nucleotide recovery pathway, is a cell-proliferation marker with potential prognostic and predictive impacts in BC. Eighty (80) cases of invasive BC with a long-term follow-up were retrospectively selected, and clinicopathological data were collected for each patient. TK1 tissue expression was evaluated immunohistochemically. Data suggested that TK1 expression levels are positively correlated with ER and PgR expression, and negatively correlated with HER2 status and the impact on patients’ distant recurrence-free survival (DRFS): in detail, among patients undergoing adjuvant chemotherapy, lower TK1 levels are correlated with better DRFS. Therefore, these results contribute to furthering the knowledge of TK1, suggesting a possible and important role of this enzyme as a biomarker in the stratification of BC patients.

Details

Language :
English
Database :
OpenAIRE
Journal :
Journal of Clinical Medicine, Volume 10, Issue 22, Journal of Clinical Medicine, Vol 10, Iss 5416, p 5416 (2021)
Accession number :
edsair.doi.dedup.....36a68ec72862277d96cb59a2dcd0df49