PIK3CA and TP53 MUTATIONS and SALL4, PTEN and PIK3R1 GENE EXPRESSION LEVELS in BREAST CANCER

Author:

Dirican Ebubekir12,Erbarut Seven İpek3,Kaya Handan3,Uğurlu M. Ümit4,Peker İrem1,Güllüoğlu Bahadır M.4,Özer Ayşe1,Akkiprik Mustafa1

Affiliation:

1. Department of Medical Biology, Marmara University Faculty of Medicine, Istanbul, Turkey

2. Istanbul Aydın University, Vocational School of Health Services, Istanbul, Turkey

3. Department of Pathology, Marmara University Faculty of Medicine, Istanbul, Turkey

4. Department of General Surgery, Marmara University Faculty of Medicine, Istanbul, Turkey

Abstract

AbstractObjectiveA high frequency of PI3K signalling pathway abnormalities and TP53 mutations are critical in the development and progression of breast cancer (BCa). We aimed to detect PIK3CA and TP53 mutations via an expression analysis of PIK3R1, PTEN and SALL4 and correlate the expression of these genes with clinical parameters of BCa.Materials and methodsPIK3CA and TP53 mutations in BCa samples were analysed by High-Resolution Melting (HRM) analysis, followed by Sanger sequencing, and the expression levels of PIK3R1, PTEN and SALL4 were evaluated by RT-PCR methods.ResultsThe frequency of PIK3CA and TP53 mutations was 42% and 38% according to the HRM and Sanger sequencing. There was a significantly high frequency of these mutations in ER( +), N0 and HER2( −) tumour samples. PIK3R1 and PTEN expression levels were high in tumour samples, whereas SALL4 expression was low. In patients with TP53 mutations, PIK3R1 expression was low, and this finding was statistically significant. PIK3R1 and PTEN expression levels showed statistically significant, respectively in G3 grades, ER(+), (PR)( +), HER2(+) and ER( +).ConclusionsWe suggest that these candidate genes could be potential prognostic biomarkers of BCa and that they should be considered in the evaluation of clinical parameters of BCa.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry, medical,Clinical Biochemistry,Molecular Biology,Biochemistry

Reference64 articles.

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