Pediatric Sarcomas: The Next Generation of Molecular Studies

被引:0
|
作者
Giannikopoulos, Petros [1 ]
Parham, David M. [2 ,3 ]
机构
[1] Univ Calif Berkeley, Innovat Genom Inst, Berkeley, CA 94704 USA
[2] Childrens Hosp Los Angeles, Dept Anat Pathol, Los Angeles, CA 90027 USA
[3] Univ Southern Calif, Keck Sch Med, Dept Pathol, Los Angeles, CA 90033 USA
关键词
pediatric sarcoma; molecular genetics; technology; scRNA seq; spatial multi-omics; high-throughput functional genomics; CRISPR-Cas9; specimen annotation; SOFT-TISSUE SARCOMAS; WIDE CRISPR SCREEN; GENETIC SCREENS; EWING SARCOMA; INTRATUMORAL HETEROGENEITY; DEVELOPMENTAL TRAJECTORIES; INTERNATIONAL SOCIETY; RISK RHABDOMYOSARCOMA; SOLID TUMORS; RNA;
D O I
10.3390/cancers14102515
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pediatric sarcomas constitute one of the largest groups of childhood cancers, following hematopoietic, neural, and renal lesions. Partly because of their diversity, they continue to offer challenges in diagnosis and treatment. In spite of the diagnostic, nosologic, and therapeutic gains made with genetic technology, newer means for investigation are needed. This article reviews emerging technology being used to study human neoplasia and how these methods might be applicable to pediatric sarcomas. Methods reviewed include single cell RNA sequencing (scRNAseq), spatial multi-omics, high-throughput functional genomics, and clustered regularly interspersed short palindromic sequence-Cas9 (CRISPR-Cas9) technology. In spite of these advances, the field continues to be challenged by a dearth of properly annotated materials, particularly from recurrences and metastases and pre- and post-treatment samples.
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页数:17
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