Abstract 662: Impact of chemotherapy on the intestinal microbiome and epithelial barrier in PDX models of lung cancer

Cindy Pensec, D. Guenot, L. Calvet, C. Mignard, O. Duchamp, T. Carton, S. Leuillet, H. Blottière, F. Vacon
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Abstract

Introduction In the field of lung cancer treatments, significant progresses have been realized during last decade, such as targeted therapies and immunotherapies. Nevertheless, chemotherapy remains the gold standard for cancer. Pemetrexed is a chemotherapeutic agent commonly used in advanced lung cancer. This drug has a broad-spectrum effect that can induce significant side effects in patients. However, the impact of pemetrexed on gut microbiota and gastrointestinal inflammation in PDX mice remains unknown, although the role of the microbiota in carcinogenesis and modulation of efficacy or toxicity of chemotherapy agents has been demonstrated. The aim of this new study was to explore the impact of pemetrexed on the gut microbiota and the integrity of intestinal epithelial barrier and inflammation markers of PDX models following treatment. Methods Upon establishment of the PDX model, mice were treated with pemetrexed for 2 weeks. Stool specimens were collected at 3 time-points: before, after and one week after treatment. Gut microbiota composition was studied by 16S rRNA gene sequencing. The colon integrity of the epithelial barrier was evaluated by a histological examination, a permeability measurement and a selected cytokines expression. In parallel, body weight was recorded and tissues were sampled for assessment of toxicity and inflammation. Results Pemetrexed induced a significant body weight loss after each treatment cycle reflecting toxicity as known in clinical results. We have found that pemetrexed and tumor induced several modifications on microbiota composition, and the more important perturbation was the significant increase of the relative abundance of Enterobacteriaceae. A significant alteration of epithelial barrier integrity associated with early inflammation and infiltration of leukocytes into mucosal tissues was observed following treatment. Moreover, we have shown that pemetrexed effect on the microbiota was reproducible on several models of lung PDX models of lung carcinoma, and that dysbiosis seem proportional to the effectiveness of chemotherapy. Conclusion This work is a preliminary approach, that confirms the relationship between microbiota and chemotherapy. A better understanding of gut microbiota alterations induced by chemotherapy could help reduce side effects. It is essential to expand our knowledge about the chemotherapy impact on microbiota in order to minimize the side effects, avoid infection complications, and improve therapy efficiency. Citation Format: Cindy Pensec, Dominique Guenot, Loreley Calvet, Caroline Mignard, Olivier Duchamp, Thomas Carton, Sebastien Leuillet, Herve M. Blottiere, Francoise Le Vacon. Impact of chemotherapy on the intestinal microbiome and epithelial barrier in PDX models of lung cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr 662.
662:化疗对肺癌PDX模型肠道微生物组和上皮屏障的影响
在肺癌治疗领域,近十年来取得了重大进展,如靶向治疗和免疫治疗。然而,化疗仍然是治疗癌症的黄金标准。培美曲塞是一种常用的化疗药物,用于晚期肺癌。该药物具有广谱作用,可引起患者明显的副作用。然而,培美曲塞对PDX小鼠肠道微生物群和胃肠道炎症的影响尚不清楚,尽管微生物群在癌变和化疗药物疗效或毒性调节中的作用已被证实。这项新研究的目的是探讨培美曲塞对PDX模型治疗后肠道微生物群、肠上皮屏障完整性和炎症标志物的影响。方法小鼠PDX模型建立后,给予培美曲塞治疗2周。在治疗前、治疗后和治疗后1周3个时间点采集粪便标本。采用16S rRNA基因测序法研究肠道菌群组成。通过组织学检查、渗透性测量和选定的细胞因子表达来评估结肠上皮屏障的完整性。同时,记录体重并取样组织以评估毒性和炎症。结果培美曲塞在每个治疗周期后都能引起明显的体重减轻,这反映了临床结果中已知的毒性。我们发现培美曲塞和肿瘤诱导了微生物群组成的一些变化,更重要的扰动是肠杆菌科相对丰度的显著增加。治疗后观察到与早期炎症和白细胞浸润粘膜组织相关的上皮屏障完整性的显著改变。此外,我们已经证明培美曲塞对微生物群的影响在肺癌的几种肺PDX模型中是可重复的,并且生态失调似乎与化疗的有效性成正比。结论本工作为确认微生物群与化疗之间的关系提供了初步途径。更好地了解化疗引起的肠道菌群改变有助于减少副作用。为了减少副作用,避免感染并发症,提高治疗效率,有必要扩大我们对化疗对微生物群影响的认识。引文格式:Cindy Pensec, Dominique Guenot, Loreley Calvet, Caroline Mignard, Olivier Duchamp, Thomas Carton, Sebastien Leuillet, Herve M. Blottiere, Francoise Le Vacon。化疗对肺癌PDX模型肠道微生物组和上皮屏障的影响[摘要]。摘自:2019年美国癌症研究协会年会论文集;2019年3月29日至4月3日;亚特兰大,乔治亚州。费城(PA): AACR;癌症杂志,2019;79(13增刊):662。
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