Division of Pulmonary and Critical Care Medicine, New York University School of Medicine, New York, New York.
Division of Pulmonary and Critical Care Medicine, VA New York Harbor Healthcare System, New York, New York.
Cancer Discov. 2021 Feb;11(2):293-307. doi: 10.1158/2159-8290.CD-20-0263. Epub 2020 Nov 11.
In lung cancer, enrichment of the lower airway microbiota with oral commensals commonly occurs, and models support that some of these bacteria can trigger host transcriptomic signatures associated with carcinogenesis. Here, we show that this lower airway dysbiotic signature was more prevalent in the stage IIIB-IV tumor-node-metastasis lung cancer group and is associated with poor prognosis, as shown by decreased survival among subjects with early-stage disease (I-IIIA) and worse tumor progression as measured by RECIST scores among subjects with stage IIIB-IV disease. In addition, this lower airway microbiota signature was associated with upregulation of the IL17, PI3K, MAPK, and ERK pathways in airway transcriptome, and we identified as the most abundant taxon driving this association. In a KP lung cancer model, lower airway dysbiosis with led to decreased survival, increased tumor burden, IL17 inflammatory phenotype, and activation of checkpoint inhibitor markers. SIGNIFICANCE: Multiple lines of investigation have shown that the gut microbiota affects host immune response to immunotherapy in cancer. Here, we support that the local airway microbiota modulates the host immune tone in lung cancer, affecting tumor progression and prognosis...
在肺癌中,常见口腔共生菌在下呼吸道微生物群中富集,模型支持其中一些细菌可以触发与癌变相关的宿主转录组特征。在这里,我们表明,这种下呼吸道生态失调特征在 IIIB-IV 期肿瘤-淋巴结-转移肺癌组中更为普遍,与预后不良相关,表现为早期疾病(I-IIIA)患者的生存率降低,以及 IIIB-IV 期疾病患者的 RECIST 评分测量的肿瘤进展更差。此外,这种下呼吸道微生物群特征与气道转录组中 IL17、PI3K、MAPK 和 ERK 通路的上调有关,我们确定 是驱动这种关联的最丰富分类群。在 KP 肺癌模型中,与 相关的下呼吸道失调导致生存率降低、肿瘤负担增加、IL17 炎症表型和检查点抑制剂标志物的激活。意义:多项研究表明,肠道微生物群会影响癌症中免疫治疗对宿主免疫反应的影响。在这里,我们支持局部气道微生物群调节肺癌中的宿主免疫基调,影响肿瘤进展和预后。