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Prognostic Value of CD200R1 mRNA Expression in Head and Neck Squamous Cell Carcinoma

Immune system dysfunction is associated with head and neck squamous cell carcinoma (HNSCC) development and progression and immune checkpoint inhibitors have demonstrated substantial survival benefits in platinum-refractory HNSCC; therefore, we examined the prognostic value of immune-related gene (IR...

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Detalles Bibliográficos
Autores principales: Chang, Hyun, Lee, Yun-Gyoo, Ko, Yoon Ho, Cho, Jang Ho, Choi, Jong-Kwon, Park, Keon Uk, Kang, Eun Joo, Lee, Keun-Wook, Lim, Sun Min, Kim, Jin-Soo, Lee, Hyun Woo, Kim, Min Kyoung, Hwang, In Gyu, Kim, Sangwoo, Nam, Byung-Ho, Kim, Hye Ryun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408128/
https://www.ncbi.nlm.nih.gov/pubmed/32635224
http://dx.doi.org/10.3390/cancers12071777
Descripción
Sumario:Immune system dysfunction is associated with head and neck squamous cell carcinoma (HNSCC) development and progression and immune checkpoint inhibitors have demonstrated substantial survival benefits in platinum-refractory HNSCC; therefore, we examined the prognostic value of immune-related gene (IRG) expression in HNSCC. We analyzed the expression of 82 IRGs in 71 patients with HNSCC enrolled in a feasibility study for a prospective HNSCC biomarker-driven umbrella trial (Korean Cancer Study Group TRIUMPH study, NCT03292250). CD200R1 was identified as an independent prognostic factor and validated in GEO and TCGA database. CD2000R1 mRNA expression was found to be an independent favorable prognostic factor in patients with HNSCC. Moreover, CD200R1 was found to affect genes and pathways associated with the immune response, while seven differentially expressed genes (CD8A, DOK2, CX3CR1, TYROBP, CXCL9, CD300LF, IFNG) were associated with CD200R1 expression. Samples with higher CD200R1 expression displayed higher tumor-infiltrating immune cell counts both in silico and in histological analysis. These findings will help in the development of more accurate prognostic tools and suggest CD200R1 modulation as a HNSCC immunotherapy.