World Journal of Surgical Oncology (Aug 2022)

Expression profile and prognostic value of CXCR family members in head and neck squamous cell carcinoma

  • Yiming Shen,
  • Chongchang Zhou,
  • Yujie Cao,
  • Qun Li,
  • Hongxia Deng,
  • Shanshan Gu,
  • Yidong Wu,
  • Zhisen Shen

DOI
https://doi.org/10.1186/s12957-022-02713-z
Journal volume & issue
Vol. 20, no. 1
pp. 1 – 15

Abstract

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Abstract Background CXC chemokine receptor gene family consists of seven well-established members which are broadly involved in biological functions of various cancers. Currently, limited studies have shed light on the expression profile of CXCR family members (CXCRs), as well as their prognostic value, in head and neck squamous cells carcinoma (HNSCC). Methods The data for this study were retrieved from the Cancer Genome Atlas database and other publicly available databases, including gene expression, methylation profiles, clinical information, immunological features, and prognoses. The expression pattern and prognostic values of CXCRs were identified, and the potential mechanism underlying CXCRs function in HNSCC was investigated by gene set enrichment analysis (GSEA). Results CXCRs were differentially expressed in HNSCC. As shown by Kaplan–Meier analysis, high CXCR3-6 expression was significantly associated with better prognostic outcomes of HNSCC patients, including overall survival and progression-free survival. According to the results of univariate and multivariate Cox proportional risk regression analysis, it was demonstrated that upregulation of CXCR3-6 was an independent factor for better prognosis, while the two other clinical features, age and stage, were factors for worse prognosis. A significant positive correlation between CXCR3-6 and tumor-infiltrated immune cells was revealed by results from Tumor Immune Estimation Resource and CIBERSORT analysis database. The main involvement of CXCRs in immune and inflammatory responses was further confirmed by GSEA. Conclusions Overall, this study provided a rationale for targeting CXCRs as a promising therapeutic strategy of HNSCC.

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