Publication:
pFAK-Y397 overexpression as both a prognostic and a predictive biomarker for patients with metastatic osteosarcoma

dc.contributor.authorKamolrat Thanapprapasren_US
dc.contributor.authorAdisak Nartthanarungen_US
dc.contributor.authorDuangmani Thanapprapasren_US
dc.contributor.authorArtit Jinawathen_US
dc.contributor.otherThailand National Metal and Materials Technology Centeren_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherBangkok Hospital Medical Centeren_US
dc.date.accessioned2018-12-21T06:26:41Z
dc.date.accessioned2019-03-14T08:02:22Z
dc.date.available2018-12-21T06:26:41Z
dc.date.available2019-03-14T08:02:22Z
dc.date.issued2017-08-01en_US
dc.description.abstract© 2017 Thanapprapasr et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Focal adhesion kinase (FAK) is important for tumor cell survival and metastasis in various cancers. However, its expression and prognostic value in patients with metastatic osteosarcoma remain unknown. We investigated the expression of FAK and its phosphorylated form (pFAK-Y397) in osteosarcoma tissues from 53 patients by immunohistochemistry and evaluated their correlations with clinicopathologic characteristics and outcomes. The prognostic values were assessed using Kaplan-Meier survival and Cox regression analyses. Total FAK and pFAK-Y397 were overexpressed in 48 (90.6%) and 33 (62.3%) cases, respectively. pFAK-Y397 overexpression was correlated with poor histologic response after neoadjuvant chemotherapy in patients with osteosarcoma regardless of the presence of metastasis or not. Kaplan-Meier curve showed that patients with metastatic osteosarcoma with pFAK-Y397 overexpression had significantly worse overall survival (OS) than those with non-overexpression (P = 0.044). Multivariate Cox regression analysis confirmed pFAK-Y397 overexpression as an independent prognostic predictor for OS and post metastases OS (PMOS) (P = 0.017, P = 0.006, respectively). Age at diagnosis was also an independent indicator for PMOS (P = 0.003). However, total FAK expression was not correlated with any clinicopathologic characteristics or OS in patients with metastatic osteosarcoma. In conclusion, our findings identified FAK as a common aberrant protein overexpression in various subtypes of osteosarcoma. pFAK-Y397 overexpression can be used as a prognostic biomarker predicting poor OS for patients with metastatic osteosarcoma, and the expression of pFAK-Y397 differentiated good and poor responders to neoadjuvant chemotherapy.en_US
dc.identifier.citationPLoS ONE. Vol.12, No.8 (2017)en_US
dc.identifier.doi10.1371/journal.pone.0182989en_US
dc.identifier.issn19326203en_US
dc.identifier.other2-s2.0-85028548018en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/41409
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85028548018&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titlepFAK-Y397 overexpression as both a prognostic and a predictive biomarker for patients with metastatic osteosarcomaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85028548018&origin=inwarden_US

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