Molecular pathological analysis of sarcomas using paraffin-embedded tissue: current limitations and future possibilities

被引:12
作者
van de Rijn, Matt [1 ]
Guo, Xiangqian [1 ]
Sweeney, Robert T. [1 ]
Beck, Andrew H. [2 ,3 ]
West, Robert B. [1 ]
机构
[1] Stanford Univ, Med Ctr, Dept Pathol, Stanford, CA 94305 USA
[2] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
关键词
molecular testing; next-generation sequencing; sarcoma; ENDOMETRIAL STROMAL SARCOMA; LONG NONCODING RNAS; FFPE TUMOR-TISSUES; GIANT-CELL TUMOR; BREAST-CARCINOMA; COPY-NUMBER; GENE-EXPRESSION; HIGH-GRADE; FUSION; TRANSLOCATION;
D O I
10.1111/his.12290
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sarcomas of soft tissue and bone are rare neoplasms that can be separated into a large number of different diagnostic entities. Over the years, a number of diagnostic markers have been developed that aid pathologists in reaching the appropriate diagnoses. Many of these markers are sarcoma-specific proteins that can be detected by immunohistochemistry in formalin-fixed, paraffin-embedded (FFPE) sections. In addition, a wide range of molecular studies have been developed that can detect gene mutations, gene amplifications or chromosomal translocations in FFPE material. Until recently, most sequencing-based approaches relied on the availability of fresh frozen tissue. However, with the advent of next-generation sequencing technologies, FFPE material is increasingly being used as a tool to identify novel immunohistochemistry markers, gene mutations, and chromosomal translocations, and to develop diagnostic tests.
引用
收藏
页码:163 / 170
页数:8
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