Regulation of metastatic organotropism

被引:2
|
作者
Dunbar, Karen J. [1 ]
Efe, Gizem [1 ,2 ]
Cunningham, Katherine [1 ,2 ]
Esquea, Emily [1 ,2 ]
Navaridas, Raul [1 ,2 ]
Rustgi, Anil K. [1 ,2 ,3 ]
机构
[1] Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
[2] Columbia Univ, Vagelos Coll Phys & Surg, Irving Med Ctr, New York, NY 10032 USA
[3] Columbia Univ, Vagelos Coll Phys & Surg, Div Digest & Liver Dis, Irving Med Ctr, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
BREAST-CANCER; LIVER METASTASIS; LUNG; NICHE; MICROENVIRONMENT; COLONIZATION; DETERMINANTS; PLASTICITY; PATTERNS; CELLS;
D O I
10.1016/j.trecan.2024.11.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastasis is responsible for most cancer-related deaths. Different cancers their own preferential sites of metastases, a phenomenon termed metastatic organotropism. The mechanisms underlying organotropism are multifactorial include the generation of a pre-metastatic niche (PMN), metastatic homing, zation, dormancy, and metastatic outgrowth. Historically, studies of metastatic organotropism have been limited by a lack of models allowing direct comparison of cells exhibiting different patterns of tropism. However, new innovative and large-scale sequencing efforts have propelled organotropism research. Herein, we summarize the recent discoveries in metastatic organotropism tion, focusing on lung, liver, brain, and bone tropism. We discuss how emerging technologies are continuing to improve our ability to model and, hopefully, and treat organotropism.
引用
收藏
页码:216 / 231
页数:16
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