Association between inflammatory infiltrates and isolated monosomy 22/del(22q) in meningiomas

• Autor(a) principal: Domingues, Patrícia Henriques
• Data de Publicação: 2013
• Outros Autores: Teodósio, Cristina, Otero, Álvaro, Sousa, Pablo, Ortiz, Javier, Macias, María del Carmen García, Gonçalves, Jesús María, Nieto, Ana Belén, Lopes, Maria Celeste, Oliveira, Catarina de, Orfão, Alberto, Tabernero, María Dolores
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/10316/109786; https://doi.org/10.1371/journal.pone.0074798
• topic: Adult; Aged; Aged, 80 and over; Antigen-Presenting Cells; Chromosomes, Human, Pair 22; Female; Humans; Inflammation; Karyotype; Lymphocytes; Male; Meningeal Neoplasms; Meningioma; Middle Aged; Transcriptome; Young Adult; Chromosome Deletion

Meningiomas contain highly variable levels of infiltrating tissue macrophages (TiMa) and other immune cells. In this study we investigated the potential association between the number and immunophenotype of inflammatory and other immune cells infiltrating the tumor as evaluated by multiparameter flow cytometry, and the clinico-biological, cytogenetic and gene expression profile (GEP) of 75 meningioma patients. Overall, our results showed a close association between the amount and cellular composition of the inflammatory and other immune cell infiltrates and the cytogenetic profile of the tumors. Notably, tumors with isolated monosomy 22/del(22q) showed greater numbers of TiMa, NK cells and (recently)-activated CD69(+) lymphocytes versus meningiomas with diploid and complex karyotypes. In addition, in the former cytogenetic subgroup of meningiomas, tumor-infiltrating TiMa also showed a more activated and functionally mature phenotype, as reflected by a greater fraction of CD69(+), CD63(+), CD16(+) and CD33(+) cells. GEP at the mRNA level showed a unique GEP among meningiomas with an isolated monosomy 22/del(22q) versus all other cases, which consisted of increased expression of genes involved in inflammatory/immune response, associated with an M1 TiMa phenotype. Altogether, these results suggest that loss of expression of specific genes coded in chromosome 22 (e.g. MIF) is closely associated with an increased homing and potentially also anti-tumoral effect of TiMa, which could contribute to explain the better outcome of this specific good-prognosis cytogenetic subgroup of meningiomas.