Sugiyama Shigeaki, Yumimoto Kanae, Nakayama Keiichi I
Department of Molecular and Cellular Biology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Department of Molecular Biology, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Cancer Med. 2025 Jan;14(1):e70557. doi: 10.1002/cam4.70557.
Metastasis is the major cause of cancer-related mortality. The premetastatic niche is a promising target for its prevention. However, the generality and cellular dynamics in premetastatic niche formation have remained unclear.
This study aimed to elucidate the generality and cellular dynamics in premetastatic niche formation.
We performed comprehensive flow cytometric analysis of lung and peripheral immune cells at three time points (early premetastatic, late premetastatic, and micrometastatic phases) for mice with subcutaneous implants of three types of cancer cells (breast cancer, lung cancer, or melanoma cells). The immuno-cell profiles were then used to predict the metastatic phase by machine learning.
We found a common pattern of changes in both lung and peripheral immune cell profiles across the three cancer types, including a decrease in the proportion of eosinophils in the early premetastatic phase, an increase in that of regulatory T cells in the late premetastatic phase, and an increase in that of polymorphonuclear myeloid-derived suppressor cells and a decrease in that of B cells in the micrometastatic phase. Machine learning using immune cell profiles could predict the metastatic phase with approximately 75% accuracy.
Validation of our findings in humans will require data on the presence or absence of micrometastases in patients and the accumulation of comprehensive and temporal information on immune cells. In addition, blood proteins, extracellular vesicles, DNA, RNA, or metabolites may be useful for more accurate prediction.
The discovery of generalities in premetastatic niche formation allow prediction of metastatic phase and provide a basis for the development of methods for early detection and prevention of cancer metastasis in a cancer type-independent manner.
转移是癌症相关死亡的主要原因。转移前生态位是预防转移的一个有前景的靶点。然而,转移前生态位形成的普遍性和细胞动力学仍不清楚。
本研究旨在阐明转移前生态位形成的普遍性和细胞动力学。
我们对皮下植入三种癌细胞(乳腺癌、肺癌或黑色素瘤细胞)的小鼠在三个时间点(转移前期早期、转移前期晚期和微转移期)的肺和外周免疫细胞进行了全面的流式细胞术分析。然后利用免疫细胞谱通过机器学习预测转移阶段。
我们发现三种癌症类型的肺和外周免疫细胞谱都有共同的变化模式,包括转移前期早期嗜酸性粒细胞比例下降,转移前期晚期调节性T细胞比例增加,微转移期多形核髓源性抑制细胞比例增加而B细胞比例下降。利用免疫细胞谱进行的机器学习能够以约75%的准确率预测转移阶段。
在人类中验证我们的发现需要患者有无微转移的数据以及关于免疫细胞的全面和动态信息的积累。此外,血液蛋白、细胞外囊泡、DNA、RNA或代谢物可能有助于更准确的预测。
转移前生态位形成普遍性的发现有助于预测转移阶段,并为以与癌症类型无关的方式开发癌症转移早期检测和预防方法提供基础。