Toby Robins Breast Cancer Now Research Centre, Breast Cancer Research Division, The Institute of Cancer Research, London, UK.
King's Health Partners Cancer Biobank, Guy's Comprehensive Cancer Centre, London, UK.
J Pathol. 2020 Mar;250(3):262-274. doi: 10.1002/path.5367. Epub 2019 Dec 22.
Understanding how breast cancer (BC) grows in axillary lymph nodes (ALNs), and refining how therapies might halt that process, is clinically important. However, modelling the complex ALN microenvironment is difficult, and no human models exist at present. We harvested ALNs from ten BC patients, and perfused them at 37 °C ex vivo for up to 24 h. Controlled autologous testing showed that ALNs remain viable after 24 h of ex vivo perfusion: haematoxylin and eosin-stained histological appearance and proliferation (by Ki67 immunohistochemistry) did not change significantly over time for any perfused ALN compared with a control from time-point zero. Furthermore, targeted gene expression analysis (NanoString PanCancer IO360 panel) showed that only 21/750 genes were differentially expressed between control and perfused ALNs (|log FC| > 1 and q < 0.1): none were involved in apoptosis and metabolism, but rather all 21 genes were involved in immune function and angiogenesis. During perfusion, tissue acid-base balance remained stable. Interestingly, the flow rate increased (p < 0.001) in cancer-replaced (i.e. metastasis occupied more than 90% of the surface area on multiple levels) compared to cancer-free nodes (i.e. nodes with no metastasis on multiple sections). CXCL11 transcripts were significantly more abundant in cancer-replaced nodes, while CXCL12 transcripts were significantly more abundant in cancer-free nodes. These cytokines were also detected in the circulating perfusate. Monoclonal antibodies (nivolumab and trastuzumab) were administered into a further three ALNs to confirm perfusion efficacy. These drugs saturated the nodes; nivolumab even induced cancer cell death. Normothermic ALN perfusion is not only feasible but sustains the tumour microenvironment ex vivo for scientific investigation. This model could facilitate the identification of actionable immuno-oncology targets. © 2019 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
了解乳腺癌(BC)如何在腋窝淋巴结(ALN)中生长,并改进可能阻止该过程的治疗方法,在临床上很重要。然而,建模复杂的 ALN 微环境具有挑战性,目前尚无人类模型。我们从十名 BC 患者中采集 ALN,并在 37°C 下进行长达 24 小时的体外灌注。对照自体检测表明,ALN 在 24 小时的体外灌注后仍保持活力:与零时的对照相比,任何灌注的 ALN 的苏木精和伊红染色组织外观和增殖(通过 Ki67 免疫组化)随时间的变化均不显著。此外,靶向基因表达分析(NanoString PanCancer IO360 面板)显示,在对照和灌注的 ALN 之间,只有 21/750 个基因的表达存在差异(|log FC|>1 和 q<0.1):没有一个基因涉及凋亡和代谢,而是所有 21 个基因都参与免疫功能和血管生成。在灌注过程中,组织酸碱平衡保持稳定。有趣的是,在癌取代的淋巴结中(即转移占据多个层面的表面积超过 90%),与无癌淋巴结(即多个切片上无转移的淋巴结)相比,流量增加(p<0.001)。在癌取代的淋巴结中,CXCL11 转录本明显更丰富,而在无癌淋巴结中,CXCL12 转录本明显更丰富。这些细胞因子也在循环灌流液中被检测到。将单克隆抗体(nivolumab 和 trastuzumab)注入另外三个 ALN 中以确认灌注效果。这些药物使淋巴结饱和,甚至诱导癌细胞死亡。体温 ALN 灌注不仅可行,而且还能维持肿瘤微环境的体外科学研究。该模型可以促进可操作的免疫肿瘤学靶点的识别。©2019 作者。约翰威立父子公司代表英国和爱尔兰病理学学会出版的《病理学杂志》。