Application of liquid biopsy in bone and soft tissue sarcomas: Present and future

被引:44
作者
Li, Xiaoyang [1 ,2 ]
Seebacher, Nicole A. [2 ]
Hornicek, Francis J. [2 ]
Xiao, Tao [1 ]
Duan, Zhenfeng [2 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Orthoped, Changsha 410011, Hunan, Peoples R China
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Orthopaed Surg, Sarcoma Biol Lab, 615 Charles E Young Dr S, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
Bone and soft tissue sarcomas; Circulating tumor cells; Circulating cell-free nucleic acids; Exosomes; Metabolites; CIRCULATING TUMOR-CELLS; POTENTIAL SERUM BIOMARKER; PERIPHERAL-BLOOD; PROGNOSTIC BIOMARKER; HUMAN OSTEOSARCOMA; EWINGS-SARCOMA; EXTRACELLULAR VESICLES; LACTATE-DEHYDROGENASE; ALKALINE-PHOSPHATASE; MITOCHONDRIAL-DNA;
D O I
10.1016/j.canlet.2018.09.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bone and soft tissue sarcomas account for approximately 1% of adult solid malignancies and 20% of pediatric solid malignancies. Sarcomas are divided into more than 50 subtypes. Each subtype is highly heterogeneous and characterized by significant morphological and phenotypic variability. Currently, sarcoma characterization is based on tissue biopsies. However, primary and invasive tissue biopsies may not accurately reflect the current disease condition following treatment as is may cause marked changes to the tumor cells. Liquid biopsy offers an alternative minimally invasive approach to provide dynamic tumor information, allowing for the application of precision medicine in the treatment of sarcomas. Recently, there have been numerous blood-based tumor components identified by liquid biopsy in sarcomas, including circulating tumor cells, circulating cell-free nucleic acids, tumor-derived exosomes and metabolites in circulation. Here, we summarize the current evolving technologies and then elaborate on emerging novel concepts that may further propel the field of liquid biopsy in sarcomas. We address the applications in the context of our current knowledge about liquid biopsy in sarcomas and highlight the potential of translating these recent advances into the clinic for more effective management strategies for sarcoma patients.
引用
收藏
页码:66 / 77
页数:12
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