Clonal tracking in cancer and metastasis

被引:3
作者
Aalam, Syed Mohammed Musheer [1 ]
Nguyen, Long Viet [2 ,3 ,4 ]
Ritting, Megan L. [1 ]
Kannan, Nagarajan [1 ,5 ,6 ]
机构
[1] Mayo Clin, Dept Lab Med & Pathol, 200 First St SW, Rochester, MN 55905 USA
[2] Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
[3] Univ Toronto, Dept Med, Toronto, ON, Canada
[4] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[5] Mayo Clin, Mayo Clin Comprehens Canc Ctr, Rochester, MN 55905 USA
[6] Mayo Clin, Ctr Regenerat Biotherapeut, Rochester, MN 55905 USA
关键词
Cellular barcoding; Clonal tracking; Cancer stem cells; Clonal dynamics; GREEN FLUORESCENT PROTEIN; ACUTE MYELOID-LEUKEMIA; STEM-CELLS; HEMATOPOIETIC STEM; GENE-THERAPY; LINEAGE; IDENTIFICATION; DYNAMICS; GROWTH; HETEROGENEITY;
D O I
10.1007/s10555-023-10149-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The eradication of many cancers has proven challenging due to the presence of functionally and genetically heterogeneous clones maintained by rare cancer stem cells (CSCs), which contribute to disease progression, treatment refractoriness, and late relapse. The characterization of functional CSC activity has necessitated the development of modern clonal tracking strategies. This review describes viral-based and CRISPR-Cas9-based cellular barcoding, lineage tracing, and imaging-based approaches. DNA-based cellular barcoding technology is emerging as a powerful and robust strategy that has been widely applied to in vitro and in vivo model systems, including patient-derived xenograft models. This review also highlights the potential of these methods for use in the clinical and drug discovery contexts and discusses the important insights gained from such approaches.
引用
收藏
页码:639 / 656
页数:18
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