Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX, USA; Center for Integrative Biology, Faculty of Science, Universidad Mayor, Santiago, Chile.
Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Cell. 2019 Aug 8;178(4):795-806.e12. doi: 10.1016/j.cell.2019.07.008.
Most patients diagnosed with resected pancreatic adenocarcinoma (PDAC) survive less than 5 years, but a minor subset survives longer. Here, we dissect the role of the tumor microbiota and the immune system in influencing long-term survival. Using 16S rRNA gene sequencing, we analyzed the tumor microbiome composition in PDAC patients with short-term survival (STS) and long-term survival (LTS). We found higher alpha-diversity in the tumor microbiome of LTS patients and identified an intra-tumoral microbiome signature (Pseudoxanthomonas-Streptomyces-Saccharopolyspora-Bacillus clausii) highly predictive of long-term survivorship in both discovery and validation cohorts. Through human-into-mice fecal microbiota transplantation (FMT) experiments from STS, LTS, or control donors, we were able to differentially modulate the tumor microbiome and affect tumor growth as well as tumor immune infiltration. Our study demonstrates that PDAC microbiome composition, which cross-talks to the gut microbiome, influences the host immune response and natural history of the disease.
大多数被诊断为胰腺导管腺癌 (PDAC) 的患者的存活时间不到 5 年,但仍有一小部分患者存活时间更长。在这里,我们剖析了肿瘤微生物群和免疫系统在影响长期生存方面的作用。我们使用 16S rRNA 基因测序,分析了短期生存 (STS) 和长期生存 (LTS) 的 PDAC 患者的肿瘤微生物组组成。我们发现 LTS 患者肿瘤微生物组的 alpha 多样性更高,并鉴定出一个与长期生存高度相关的肿瘤内微生物组特征 (Pseudoxanthomonas-Streptomyces-Saccharopolyspora-Bacillus clausii),在发现和验证队列中均具有预测价值。通过 STS、LTS 或对照供体的人体到小鼠粪便微生物群移植 (FMT) 实验,我们能够差异化地调节肿瘤微生物群并影响肿瘤生长和肿瘤免疫浸润。我们的研究表明,与肠道微生物群相互作用的 PDAC 微生物组组成影响宿主免疫反应和疾病的自然史。