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[Genomic profiles and immune microenvironment of olfactory neuroblastoma].
Yang, Y Y; Liu, H G; Li, Y H; Li, X C; Piao, Y S.
Afiliación
  • Yang YY; Beijing Key Laboratory of Molecular Diagnosis of Head and Neck Pathology, Department of Pathology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China.
  • Liu HG; Beijing Key Laboratory of Molecular Diagnosis of Head and Neck Pathology, Department of Pathology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China.
  • Li YH; Beijing Key Laboratory of Molecular Diagnosis of Head and Neck Pathology, Department of Pathology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China.
  • Li XC; Beijing Key Laboratory of Molecular Diagnosis of Head and Neck Pathology, Department of Pathology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China.
  • Piao YS; Beijing Key Laboratory of Molecular Diagnosis of Head and Neck Pathology, Department of Pathology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China.
Zhonghua Bing Li Xue Za Zhi ; 53(9): 916-921, 2024 Sep 08.
Article en Zh | MEDLINE | ID: mdl-39231744
ABSTRACT

Objective:

To investigate the genomic profiles and immune microenvironment of olfactory neuroblastoma (ONB).

Methods:

Nineteen ONB cases diagnosed in the Beijing Tongren Hospital from May 2018 to October 2022 were divided into low-grade and high-grade groups according to the Hyams grading system, including 7 low-grade and 12 high-grade ONB. Whole exome sequencing and multiplex immunofluorescence analyses were performed on tissue samples of these ONB.

Results:

A total of 929 nonsynonymous alterations were identified in 18 of the 19 ONB (18/19) cases. The most commonly altered cancer-related genes were CTNNB1 (3/19) and ZNRF3 (3/19). The most mutated oncogenic pathways were the WNT and RAS pathways. The median tumor mutation burden (TMB) was 0.45/Mb, ranging from 0 to 3.25. The median tumor neoantigen load (TNB) was 9.39 neoantigens/Mb, ranging from 0 to 38.30. The median allelic mutation tumor heterogeneity (MATH) score was 16.95, ranging from 3.05 to 117.47. Only one of the 19 cases expressed PD-L1 (composite positive score, CPS>1) in the tumor cells. The median percentage of CD8+ tumor-infiltrating lymphocyte (TIL) in the tumor region was 1.08%. No significant differences were observed between the low-and high-grade groups for mutant genes, mutant pathways, TMB, TNB, MATH, PD-L1 expression levels, or CD8+ TILs percentage(P>0.05). However, the low-grade group showed significantly more CD68+ macrophages in both the tumor and total region than the high-grade group. Notably, CD68+CD163- macrophages accounted for an average of 80.52% of CD68+ macrophages.

Conclusions:

CTNNB1 and ZNRF3 are the most commonly altered cancer-related genes. The low expression of PD-L1 and the low percentage of CD8+ TIL indicate that ONB might not be sensitive to immunotherapy. The percentage of M1-type macrophages in low-grade ONB is significantly higher than that in high-grade ONB, suggesting that M1-type macrophages may be involved in the progression of ONB from low-grade to high-grade.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Nasales / Estesioneuroblastoma Olfatorio / Microambiente Tumoral / Mutación Límite: Humans Idioma: Zh Revista: Zhonghua Bing Li Xue Za Zhi Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Nasales / Estesioneuroblastoma Olfatorio / Microambiente Tumoral / Mutación Límite: Humans Idioma: Zh Revista: Zhonghua Bing Li Xue Za Zhi Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: China