PR05:利用溶解期巨噬细胞预防乳腺癌转移生态位复发

Odelya Gilon, Y. Feuermann, Sagie Schif-Zuck, Keren Weidenfeld, P. V. Huth, E. Sabo, A. Ariel, D. Barkan
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摘要

在原发肿瘤切除和辅助治疗多年后以转移性疾病复发的乳腺癌,似乎是由肿瘤细胞在病程早期播散,但未发展成临床明显病变引起的。这些长期存活的、静止的弥散性休眠肿瘤细胞(QDTC)对靶向活跃分裂细胞的常规治疗具有耐药性。负责维持QDTC存活和生长的机制在很大程度上仍然未知。最近,我们发现在QDTC的居住部位建立了广泛沉积I型胶原(coli)和纤维蛋白的纤维样微环境,促进了QDTC的爆发。因此,我们假设,在允许部位促进消退——终止炎症和纤维化反应并积极引导组织恢复稳态的内源性机制——将使其“正常化”并防止转移性爆发。本研究表明,体外生成的促溶解CD11blow巨噬细胞分泌的可溶性因子可以抑制纤维化生态位的建立,从而抑制QDTC的转移性生长。对纤维化生态位的抑制是由于tgf β1诱导的成纤维细胞向肌成纤维细胞分化和肌成纤维细胞凋亡受到抑制。有趣的是,我们的数据还表明,阻断成纤维细胞向肌成纤维细胞分化并不是通过抑制tgf - β1的典型信号传导来介导的。综上所述,我们的研究结果展示了一种开创性的概念方法,通过促进组织分辨率轴来“正常化”支持QDTC生长的微环境。此摘要也以海报B36的形式呈现。引文格式:Odelya Gilon, Yonatan David Feuermann, Sagie Schif-Zuck, Keren Weidenfeld, Palle Von Huth, Edmond Sabo, Amiram Ariel, Dalit Barkan。利用溶解期巨噬细胞预防乳腺癌转移生态位复发[摘要]。摘自:AACR肿瘤免疫学和免疫治疗特别会议论文集;2017年10月1-4日;波士顿,MA。费城(PA): AACR;癌症免疫,2018;6(9增刊):摘要nr PR05。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract PR05: Preventing the recurrence of breast cancer at the metastatic niche using resolution-phase macrophages
Breast cancer that recurs as metastatic disease many years after primary tumor resection and adjuvant therapy appears to arise from tumor cells that disseminated early in the course of the disease but did not develop into clinically apparent lesions. These long-term surviving, quiescent disseminated dormant tumor cells (QDTC) are resistant to conventional therapies that target actively dividing cells. The mechanisms responsible for maintaining the survival and outgrowth of QDTC remain largely unknown. Recently, we found that fibrotic-like microenvironment with extensive deposition of Type I collagen (Col-I) and fibroectin, established at the site of the residing QDTC, promoted the outbreak of QDTC. Therefore, we hypothesized that promoting resolution—the endogenous mechanism that terminates inflammation and fibrotic responses and actively directs tissue return to homeostasis—at the permissive site will “normalize” it and prevent metastatic outbreak. Here we demonstrate that soluble factors secreted by ex vivo generated pro-resolving CD11blow macrophages can inhibit the establishment of a fibrotic niche resulting in the inhibition of the metastatic outgrowth of QDTC. The inhibition of the fibrotic niche was due to inhibition of TGFβ1-induced differentiation of fibroblasts to myofibroblasts and myofibroblasts’ apoptosis. Interestingly, our data also demonstrate that the blockade of fibroblast differentiation to myofibroblasts is not mediated by inhibition of the canonical signaling of TGFβ1. Taken together our results demonstrate a pioneering conceptual approach to “normalize” the microenvironment that supports the outgrowth of QDTC by promoting the tissue resolution axis. This abstract is also being presented as Poster B36. Citation Format: Odelya Gilon, Yonatan David Feuermann, Sagie Schif-Zuck, Keren Weidenfeld, Palle Von Huth, Edmond Sabo, Amiram Ariel, Dalit Barkan. Preventing the recurrence of breast cancer at the metastatic niche using resolution-phase macrophages [abstract]. In: Proceedings of the AACR Special Conference on Tumor Immunology and Immunotherapy; 2017 Oct 1-4; Boston, MA. Philadelphia (PA): AACR; Cancer Immunol Res 2018;6(9 Suppl):Abstract nr PR05.
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