Evolving cancer-niche interactions and therapeutic targets during bone metastasis

被引:66
|
作者
Satcher, Robert L. [1 ]
Zhang, Xiang H. -F. [2 ,3 ,4 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Orthoped Oncol, Houston, TX 77030 USA
[2] Baylor Coll Med, Lester & Sue Smith Breast Ctr, Houston, TX 77030 USA
[3] Baylor Coll Med, Dan L Duncan Canc Ctr, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
关键词
RENAL-CELL CARCINOMA; PROSTATIC ACID-PHOSPHATASE; HEMATOPOIETIC STEM-CELLS; DISSEMINATED TUMOR-CELLS; COLONY-STIMULATING FACTOR; PREDICTS POOR-PROGNOSIS; HORMONE-RELATED PROTEIN; BREAST-CANCER; MULTIPLE-MYELOMA; ZOLEDRONIC ACID;
D O I
10.1038/s41568-021-00406-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Many cancer types metastasize to bone. This propensity may be a product of genetic traits of the primary tumour in some cancers. Upon arrival, cancer cells establish interactions with various bone-resident cells during the process of colonization. These interactions, to a large degree, dictate cancer cell fates at multiple steps of the metastatic cascade, from single cells to overt metastases. The bone microenvironment may even influence cancer cells to subsequently spread to multiple other organs. Therefore, it is imperative to spatiotemporally delineate the evolving cancer-bone crosstalk during bone colonization. In this Review, we provide a summary of the bone microenvironment and its impact on bone metastasis. On the basis of the microscopic anatomy, we tentatively define a roadmap of the journey of cancer cells through bone relative to various microenvironment components, including the potential of bone to function as a launch pad for secondary metastasis. Finally, we examine common and distinct features of bone metastasis from various cancer types. Our goal is to stimulate future studies leading to the development of a broader scope of potent therapies.
引用
收藏
页码:85 / 101
页数:17
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