The covert symphony: cellular and molecular accomplices in breast cancer metastasis

被引:2
作者
Si, Hongjiang [1 ]
Esquivel, Madelyn [1 ]
Mendoza, Erika Mendoza [1 ]
Roarty, Kevin [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dan L Duncan Comprehens Canc Ctr, One Baylor Plaza, Houston, TX 77030 USA
关键词
breast cancer; tumor microenvironment; CTC (circulating tumor cells); dormancy; metastasis (cancer metastasis); metastatic niche; MESENCHYMAL STEM-CELLS; DORMANT TUMOR-CELLS; BONE-MARROW; UROKINASE RECEPTOR; T-CELLS; PREMETASTATIC NICHE; TENASCIN-C; PLASMINOGEN-ACTIVATOR; VASCULAR-PERMEABILITY; SIGNALING PATHWAYS;
D O I
10.3389/fcell.2023.1221784
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Breast cancer has emerged as the most commonly diagnosed cancer and primary cause of cancer-related deaths among women worldwide. Although significant progress has been made in targeting the primary tumor, the effectiveness of systemic treatments to prevent metastasis remains limited. Metastatic disease continues to be the predominant factor leading to fatality in the majority of breast cancer patients. The existence of a prolonged latency period between initial treatment and eventual recurrence in certain patients indicates that tumors can both adapt to and interact with the systemic environment of the host, facilitating and sustaining the progression of the disease. In order to identify potential therapeutic interventions for metastasis, it will be crucial to gain a comprehensive framework surrounding the mechanisms driving the growth, survival, and spread of tumor cells, as well as their interaction with supporting cells of the microenvironment. This review aims to consolidate recent discoveries concerning critical aspects of breast cancer metastasis, encompassing the intricate network of cells, molecules, and physical factors that contribute to metastasis, as well as the molecular mechanisms governing cancer dormancy.
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页数:20
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