Endothelial Cells as Precursors for Osteoblasts in the Metastatic Prostate Cancer Bone

被引:29
作者
Paiva, Ana E. [1 ]
Lousado, Luiza [1 ]
Almeida, Viviani M. [1 ]
Andreotti, Julia P. [1 ]
Santos, Gabryella S. P. [1 ]
Azevedo, Patrick O. [1 ]
Sena, Isadora F. G. [1 ]
Prazeres, Pedro H. D. M. [1 ]
Borges, Isabella T. [1 ]
Azevedo, Vasco [2 ]
Mintz, Akiva [3 ]
Birbrair, Alexander [1 ]
机构
[1] Univ Fed Minas Gerais, Dept Pathol, Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Inst Biol Sci, Dept Gen Biol, Belo Horizonte, MG, Brazil
[3] Columbia Univ, Med Ctr, Dept Radiol, New York, NY USA
来源
NEOPLASIA | 2017年 / 19卷 / 11期
基金
美国国家卫生研究院;
关键词
PHENOTYPIC HETEROGENEITY; PERICYTES PARTICIPATE; RECEPTOR; TIE2; DIFFERENTIATION; REGENERATION; EXPRESSION; DISEASE; LINEAGE; BIOLOGY;
D O I
10.1016/j.neo.2017.08.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer cells metastasize to the bones, causing ectopic bone formation, which results in fractures and pain. The cellular mechanisms underlying new bone production are unknown. In a recent study, Lin and colleagues, by using state-of-the-art techniques, including prostate cancer mouse models in combination with sophisticated in vivo lineage-tracing technologies, revealed that endothelial cells form osteoblasts induced by prostate cancer metastasis in the bone. Strikingly, genetic deletion of osteorix protein from endothelial cells affected prostate cancer-induced osteogenesis in vivo. Deciphering the osteoblasts origin in the bone microenvironment may result in the development of promising new molecular targets for prostate cancer therapy.
引用
收藏
页码:928 / 931
页数:4
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