Single-cell profiling in multiple myeloma: insights problems, and promises

被引:4
|
作者
Samur, Mehmet Kemal [1 ,2 ,6 ]
Szalat, Raphael [3 ]
Munshi, Nikhil C. [4 ,5 ,6 ]
机构
[1] Dana Farber Canc Inst, Dept Data Sci, Boston, MA USA
[2] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
[3] Boston Univ, Dept Hematol & Med Oncol, Med Ctr, Boston, MA USA
[4] Harvard Med Sch, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA USA
[5] VA Boston Healthcare Syst, Boston, MA USA
[6] Dana Farber Canc Inst, 450 Brookline Ave, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
BONE-MARROW MICROENVIRONMENT; MINIMAL RESIDUAL DISEASE; B-CELL; HETEROGENEITY; RESOLUTION;
D O I
10.1182/blood.2022017145
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In a short time, single-cell platforms have become the norm in many fields of research, including multiple myeloma (MM). In fact, the large amount of cellular heterogeneity in MM makes single-cell platforms particularly attractive because bulk assessments can miss valuable information about cellular subpopulations and cell-to-cell interactions. The decreasing cost and increasing accessibility of single-cell platform, combined with breakthroughs in obtaining multiomics data for the same cell and innovative computational programs for analyzing data, have allowed single-cell studies to make important insights into MM pathogenesis; yet, there is still much to be done. In this review, we will first focus on the types of single-cell profiling and the considerations for designing a single-cell profiling experiment. Then, we will discuss what have learned from single-cell profiling about myeloma clonal evolution, transcriptional repro-gramming, and drug resistance, and about the MM microenvironment during precursor and advanced disease.
引用
收藏
页码:313 / 324
页数:12
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