Lineage plasticity in prostate cancer: Looking beyond intrinsic alterations

被引:4
|
作者
Ferguson, Alison M. [1 ]
Rubin, Mark A. [1 ,2 ,3 ]
机构
[1] Univ Bern, Dept Biomed Res, CH-3008 Bern, Switzerland
[2] Univ Hosp Bern, Bern Ctr Precis Med, Inselspital, CH-3008 Bern, Switzerland
[3] Murtenstr 24, CH-3008 Bern, Switzerland
关键词
Prostate cancer; Lineage plasticity; Genomics; Tumour microenvironment; Extrinsic factors; Stemness; Differentiation; Therapeutic resistance; Metastatic niche; Microbiome; ANTIANDROGEN RESISTANCE; BREAST-CANCER; TUMOR-GROWTH; METASTASIS; INFLAMMATION; HYPOXIA; CELLS; MICROENVIRONMENT; FIBROBLASTS; PROGRESSION;
D O I
10.1016/j.canlet.2022.215901
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Emergence of small cell prostate cancer is linked to the plasticity of tumour cells and avoidance of environmental pressures. This process is thought to be reversable, however to-date evidence of this has been demonstrated in small-cell prostate cancer. To study the plasticity of prostate tumours, we look to clinical cohorts of patients covering the spectra of malignancy subtypes and utilise in vitro and in vivo models of disease progression. Current models have assisted in the understanding of the extremities of this plasticity, elucidating internal mechanisms and adaptations to stressors through transition to altered cell states. By interrogating the tumour microenvi-ronment and earlier time points, we are beginning to form a deeper understanding of the full spectra of tumour plasticity. It could be proffered that this deeper understanding will lead to better patient outcome, with earlier interventions more likely to reverse plasticity and prevent trans-differentiation to the aggressive, small cell phenotype.
引用
收藏
页数:6
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