Abstract LB226: Maternal microbiome protects host against clonal de novo transformation, early onset systemic metastasis, and sudden death

Nagarajan Kannan, Syed Mohammed Musheer Aalam, Xiaojia Tang, K. Kalari, P. Kashyap, Jun Chen, Stephen Johnson, A. Sadanandam, M. Sherman
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Abstract

The role of maternal microbiome transmitted at birth in cancer control is poorly understood. We have developed the first germfree B6 mouse model of breast cancer to investigate the role of the maternal microbiome in controlling oncogenic/metastatic frequencies of pro-oncogenic mammary cells. In this model, a DNA barcoded, primitive normal mouse mammary epithelial cell encoding MMTV-PyMT oncogene, was transplanted in large numbers into conventional or germfree B6 mice. Next-gen sequencing analysis of the DNA barcodes in tissues enabled us to clonally track millions of cells and measure the frequency and growth dynamics of clones at the primary site and their systemic distribution in circulation and all vital organs, generating an unprecedented high-definition map of cancer progression. Our results show that in conventional B6 mice with maternal microbial transmission at-birth, a small fraction (~0.01%) of transplanted cells transform de novo and produce slow growing, late-onset benign tumors (mouse median survival of > 1 year). In contrast, in germfree B6 mice, a >10-fold higher frequency of cells transform de novo and generate early-onset, highly aggressive metastatic clones, and are frequently associated with features leading to early euthanasia or endpoint (i.e. sudden death, intracardiac metastasis, paralysis, swollen abdomen, early multiorgan aggressive metastasis) (median survival of ~4 months; p 1 year; p Citation Format: Nagarajan Kannan, Syed Mohammed Musheer Aalam, Xiaojia Tang, Krishna Kalari, Purna Kashyap, Jun Chen, Stephen Johnson, Anguraj Sadanandam, Mark Sherman. Maternal microbiome protects host against clonal de novo transformation, early onset systemic metastasis, and sudden death [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr LB226.
摘要LB226:母体微生物组保护宿主抗克隆新生转化、早发性全身转移和猝死
出生时传播的母体微生物组在癌症控制中的作用尚不清楚。我们开发了第一个无菌B6乳腺癌小鼠模型,以研究母体微生物组在控制促癌乳腺细胞的致癌/转移频率中的作用。在该模型中,将编码MMTV-PyMT癌基因的DNA条形码原始正常小鼠乳腺上皮细胞大量移植到常规或无菌B6小鼠中。对组织中DNA条形码的下一代测序分析使我们能够对数百万个细胞进行克隆跟踪,并测量原发部位克隆的频率和生长动态,以及它们在循环系统和所有重要器官中的分布,从而生成前所未有的高清癌症进展图。我们的研究结果表明,在出生时母体微生物传播的常规B6小鼠中,一小部分(~0.01%)的移植细胞会重新转化并产生生长缓慢、晚发性的良性肿瘤(小鼠的中位生存期为100年)。相比之下,在无菌B6小鼠中,细胞新生转化和产生早发、高侵袭性转移克隆的频率高出10倍,并且经常与导致早期安乐死或终点(即猝死、心内转移、瘫痪、腹部肿胀、早期多器官侵袭性转移)的特征相关(中位生存期约4个月;P 1年;p引文格式:Nagarajan Kannan, Syed Mohammed Musheer Aalam, Xiaojia Tang, Krishna Kalari, Purna Kashyap, Jun Chen, Stephen Johnson, Anguraj Sadanandam, Mark Sherman。母体微生物组保护宿主免受克隆新生转化、早发性全身转移和猝死[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要nr LB226。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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