An Official Journal of Polish Society of Orthopaedics and Traumatology
ISSN:1897-2276
e-ISSN: 2449-9145
Mohamed Ahmed Eladl
University of Sharjah, UAE
Posters & Accepted Abstracts: J Orthop Trauma Surg Rel Res
Yes-associated protein (YAP) is an oncoprotein encoded by YAP1 gene. Hippo pathway activation results in sequestration of YAP in the cytoplasm and degradation. Whereas, when the Hippo pathway is deactivated, YAP is translocated into the nucleus and promotes transcription of downstream genes stimulating growth and inhibiting apoptosis. Numerous studies showed that overexpression of YAP induces epithelial-mesenchymal transition, inhibits apoptosis and increases cancer stem cells number in-vitro. Levels of YAP were found to be elevated in many human cancers and related to poorly differentiated tumors. Therefore, YAP has emerged as a prime target for developing anti-cancer drugs. This study aims to investigate the immunohistochemical expression of YAP in breast cancer tissue compared to benign tumors and normal breast tissue. The nuclear expression of YAP was evaluated in six cases of benign fibroadenomas, 6 cases of in- situ ductal carcinomas, 6 cases of normal breast tissue samples as well as 60 cases of invasive breast carcinoma, 57 ductal (IDC) and 3 lobular (ILC). Staining was analyzed and blindly scored. Nuclear staining of more than 20% of the nuclei was considered positive. Cytoplasmic staining was scored according to its intensity as (+1 mild, +2 moderate, +3 strong). The results were then correlated with grade, stage and hormone receptor positivity in each of those tissues. All cases of normal, benign and in-situ carcinomas depicted no nuclear YAP expression. YAP expression in these cases was mostly cytoplasmic and varied in expression between mild, moderate or strong. On the other hand, 60% of invasive breast carcinomas cases showed positive nuclear staining suggesting that YAP is active in these tumors and could have possible carcinogenic role. Our data showed that YAP is highly active in breast adenocarcinoma and suggest that further studies are required to investigate the exact pathway responsible for YAP activation and its involvement in carcinogenesis.
E-mail: meladl@sharjah.ac.ae
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