Foxp3 overexpression in tumor cells predicts poor survival in oral squamous cell carcinoma

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Foxp3 overexpression in tumor cells predicts poor survival in oral squamous cell carcinoma

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Thông tin tài liệu

Forkhead Box P3 (Foxp3) is a regulatory T cells marker, and its expression correlates with prognosis in a number of malignancies. The aim of this study is to determine the relationship of Foxp3 expression with clinicopathological parameters and prognosis in oral squamous cell carcinoma (OSCC).

Song et al BMC Cancer (2016) 16:530 DOI 10.1186/s12885-016-2419-6 RESEARCH ARTICLE Open Access Foxp3 overexpression in tumor cells predicts poor survival in oral squamous cell carcinoma Jing-Jing Song1†, Si-Jia Zhao2†, Juan Fang1, Da Ma1, Xiang-Qi Liu1, Xiao-Bing Chen1, Yun Wang1, Bin Cheng1* and Zhi Wang1* Abstract Background: Forkhead Box P3 (Foxp3) is a regulatory T cells marker, and its expression correlates with prognosis in a number of malignancies The aim of this study is to determine the relationship of Foxp3 expression with clinicopathological parameters and prognosis in oral squamous cell carcinoma (OSCC) Methods: Foxp3 expression was examined using immunohistochemistry (IHC) in paraffin-embedded tissue samples from 273 OSCC patients Statistical analysis was performed to evaluate the associations between Foxp3 expression, the clinicopathologic characteristics and prognostic factors in OSCC Results: Foxp3 protein expression was significantly associated with lymph node metastasis (P

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Mục lục

  • Abstract

    • Background

    • Methods

    • Results

    • Conclusions

    • Background

    • Methods

      • Study population

      • Tissue microarrays and IHC testing of patient samples

      • Statistical analysis

      • Results

        • Association of Foxp3 with lymph node metastasis and other clinicopathological variables

        • Relationship between Foxp3 expression and prognosis in OSCC patients

        • Discussion

        • Conclusions

        • Abbreviations

        • Acknowledgements

        • Funding

        • Availability of data and materials

        • Authors’ contributions

        • Competing interests

        • Consent for publication

        • Ethics approval and consent to participate

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