Soochow University Laboratory of Cancer Molecular Genetics, Collaborative Innovation Center of Molecular Medicine between Soochow University and Donghai County People's Hospital, Clinical Medicine Research Institute of Soochow University and Suzhou BenQ Medical Center, Suzhou Medical College of Soochow University, Suzhou, 215123, Jiangsu Province, China.
Department of Genetics, School of Basic Medical Sciences, Suzhou Medical College of Soochow University, Suzhou, 215123, Jiangsu Province, China.
Oncogene. 2024 Jul;43(28):2215-2227. doi: 10.1038/s41388-024-03072-7. Epub 2024 May 27.
Approximately 40% of patients with lung adenocarcinoma (LUAD) often develop bone metastases during the course of their disease. However, scarcely any in vivo model of LUAD bone metastasis has been established, leading to a poor understanding of the mechanisms underlying LUAD bone metastasis. Here, we established a multiorgan metastasis model via the left ventricular injection of luciferase-labeled LUAD cells into nude mice and then screened out lung metastasis (LuM) and bone metastasis (BoM) cell subpopulations. BoM cells exhibited greater stemness and epithelial-mesenchymal transition (EMT) plasticity than LuM cells and initially colonized the bone and subsequently disseminated to distant organs after being reinjected into mice. Moreover, a CD74-ROS1 fusion mutation (C6; R34) was detected in BoM cells but not in LuM cells. Mechanistically, BoM cells bearing the CD74-ROS1 fusion highly secrete the C-C motif chemokine ligand 5 (CCL5) protein by activating STAT3 signaling, recruiting macrophages in tumor microenvironment and strongly inducing M2 polarization of macrophages. BoM cell-activated macrophages produce a high level of TGF-β1, thereby facilitating EMT and invasion of LUAD cells via TGF-β/SMAD2/3 signaling. Targeting the CD74-ROS1/CCL5 axis with Crizotinib (a ROS1 inhibitor) and Maraviroc (a CCL5 receptor inhibitor) in vivo strongly impeded bone metastasis and secondary metastasis of BoM cells. Our findings reveal the critical role of the CD74-ROS1/STAT3/CCL5 axis in the interaction between LUAD bone metastasis cells and macrophages for controlling LUAD cell dissemination, highlighting the significance of the bone microenvironment in LUAD bone metastasis and multiorgan secondary metastasis, and suggesting that targeting CD74-ROS1 and CCL5 is a promising therapeutic strategy for LUAD bone metastasis.
大约 40%的肺腺癌 (LUAD) 患者在疾病过程中经常发生骨转移。然而,几乎没有建立 LUAD 骨转移的体内模型,导致对 LUAD 骨转移机制的理解很差。在这里,我们通过将荧光素酶标记的 LUAD 细胞注入裸鼠左心室建立了多器官转移模型,然后筛选出肺转移 (LuM) 和骨转移 (BoM) 细胞亚群。BoM 细胞比 LuM 细胞具有更强的干性和上皮间质转化 (EMT) 可塑性,最初在骨中定植,然后在重新注入小鼠后扩散到远处器官。此外,在 BoM 细胞中检测到 CD74-ROS1 融合突变 (C6; R34),但在 LuM 细胞中未检测到。在机制上,携带 CD74-ROS1 融合的 BoM 细胞通过激活 STAT3 信号强烈分泌 C-C 基序趋化因子配体 5 (CCL5) 蛋白,招募肿瘤微环境中的巨噬细胞,并强烈诱导巨噬细胞向 M2 极化。BoM 细胞激活的巨噬细胞产生高水平的 TGF-β1,从而通过 TGF-β/SMAD2/3 信号通路促进 LUAD 细胞的 EMT 和侵袭。体内用克唑替尼(一种 ROS1 抑制剂)和马拉维若(一种 CCL5 受体抑制剂)靶向 CD74-ROS1/CCL5 轴强烈抑制了 BoM 细胞的骨转移和继发性转移。我们的研究结果揭示了 CD74-ROS1/STAT3/CCL5 轴在 LUAD 骨转移细胞与巨噬细胞相互作用中控制 LUAD 细胞扩散的关键作用,强调了骨微环境在 LUAD 骨转移和多器官继发性转移中的重要性,并表明靶向 CD74-ROS1 和 CCL5 是治疗 LUAD 骨转移的一种有前途的治疗策略。