Bone microenvironment signaling of cancer stem cells as a therapeutic target in metastatic prostate cancer

被引:10
作者
Lee, Clara H. [1 ]
Decker, Ann M. [1 ]
Cackowski, Frank C. [1 ,2 ]
Taichman, Russell S. [1 ,3 ]
机构
[1] Univ Michigan, Sch Dent, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Internal Med, Div Hematol Oncol, Ann Arbor, MI 48109 USA
[3] Univ Alabama Birmingham, Sch Dent, Dept Periodontol, Birmingham, AL 35294 USA
关键词
Prostate cancer; Metastasis; Cancer stem cells; Bone microenvironment; Signaling pathway; Therapy; EPITHELIAL-MESENCHYMAL TRANSITION; HEDGEHOG PATHWAY INHIBITOR; RECEPTOR TYROSINE KINASE; PHASE-II; INITIATING CELLS; NOTCH PATHWAY; WNT PATHWAY; GROWTH; CASTRATION; TUMOR;
D O I
10.1007/s10565-019-09483-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Prostate cancer (PCa) is one of the most prevalent cancers and the second leading cause of cancer death among US males. When diagnosed in an early disease stage, primary tumors of PCa may be treated with surgical resection or radiation, sometimes combined with androgen deprivation therapy, with favorable outcomes. Unfortunately, the treatment efficacy of each approach decreases significantly in later stages of PCa that involve metastasis to soft tissues and bone. Metastatic PCa is a heterogeneous disease containing host cells, mature cancer cells, and subpopulation of cancer stem cells (CSC). CSCs are highly tumorigenic due to their self-renewing and differentiating potential, clinically resulting in recurrence and resistance to standard therapies. Therefore, there is a large unmet clinical need to develop therapies, which target CSC activity. In this review, we summarize the main signaling pathways that are implicated in the current pre-clinical and clinical studies of recurrent metastatic PCa within the bone microenvironment targeting CSCs and discuss the trajectory of therapeutics moving forward.
引用
收藏
页码:115 / 130
页数:16
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