Lineage Plasticity: The New Cancer Hallmark on the Block

被引:4
|
作者
Mehta, Arnav [1 ,2 ,3 ,4 ,9 ]
Stanger, Ben Z. [5 ,6 ,7 ,8 ]
机构
[1] Massachusetts Gen Hosp, Dept Med, Boston, MA USA
[2] Massachusetts Gen Hosp, Canc Ctr, Boston, MA USA
[3] Harvard Med Sch, Boston, MA USA
[4] Broad Inst MIT & Harvard, Cambridge, MA USA
[5] Univ Penn, Abramson Family Canc Res Inst, Perelman Sch Med, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Med, Perelman Sch Med, Philadelphia, PA USA
[7] Univ Penn, Perelman Sch Med, Dept Cell & Dev Biol, Philadelphia, PA USA
[8] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[9] Broad Inst MIT & Harvard, Cambridge, MA 02142, England
关键词
ACQUIRED-RESISTANCE; TUMOR-CELLS; METASTASIS; STATE; EMT; VULNERABILITY; SUBTYPES; THERAPY; MODE; RB1;
D O I
10.1158/0008-5472.CAN-23-1067
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Plasticity refers to the ability of cells to adopt a spectrum of states or phenotypes. In cancer, it is a critical contributor to tumor initiation, progression, invasiveness, and therapy resistance, and it has recently been recognized as an emerging cancer hallmark. Plasticity can occur as a result of cell-intrinsic factors (e.g., genetic, transcriptional, or epigenetic fluctuations), or through cell-extrinsic cues (e.g., signaling from components of the tumor microenvironment or selective pressure from therapy). Over the past decade, technological advances, analysis of patient samples, and studies in mouse model systems have led to a deeper understanding of how such plastic states come about. In this review, we discuss: (i) the definition of plasticity; (ii) methods to measure and quantify plasticity; (iii) the clinical relevance of plasticity; and (iv) therapeutic hypotheses to modulate plasticity in the clinic.
引用
收藏
页码:184 / 191
页数:8
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