Department of Pathology, Wayne State University School of Medicine, 540 East Canfield Avenue, Detroit, MI, 48201, USA.
Department of Oncology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Cancer Metastasis Rev. 2018 Dec;37(4):655-663. doi: 10.1007/s10555-018-9767-4.
The predominant cause of cancer mortality is metastasis. The major impediment to cancer cure is the intrinsic or acquired resistance to currently available therapies. Cancer is heterogeneous at the genetic, epigenetic, and metabolic levels. And, while a molecular-targeted drug may be pathway-precise, it can still fail to achieve wholesome cancer-precise toxicity. In the current review, we discuss the strategic differences between targeting the strengths of cancer cells in phenotypic plasticity and heterogeneity and targeting shared vulnerabilities of cancer cells such as the compromised integrity of membranous organelles. To better recapitulate subpopulations of cancer cells in different phenotypic and functional states, we developed a schematic combination of 2-dimensional culture (2D), 3-dimmensional culture in collagen I (3D), and mammosphere culture for stem cells (mammosphere), designated as Scheme 2D/3D/mammosphere. We investigated how the tumor suppressor maspin may limit carcinoma cell plasticity and affect their context-dependent response to drugs of different mechanisms including docetaxel, histone deacetylase (HDAC) inhibitor MS-275, and ionophore antibiotic salinomycin. We showed that tumor cell phenotypic plasticity is not an exclusive attribute to cancer stem cells. Nonetheless, three subpopulations of prostate cancer cells, enriched through Scheme 2D/3D/mammosphere, show qualitatively different drug responses. Interestingly, salinomycin was the only drug that effectively killed all three cancer cell subpopulations, irrespective of their capacity of stemness. Further, Scheme 2D/3D/mammosphere may be a useful model to accelerate the screening for curative cancer drugs while avoiding costly characterization of compounds that may have only selective toxicity to some, but not all, cancer cell subpopulations.
癌症死亡的主要原因是转移。癌症治疗的主要障碍是对现有治疗方法的内在或获得性耐药。癌症在遗传、表观遗传和代谢水平上具有异质性。虽然针对特定分子的药物可能在途径上是精确的,但它仍然可能无法实现针对癌症的全面毒性。在当前的综述中,我们讨论了针对癌细胞表型可塑性和异质性的优势与针对细胞膜细胞器完整性受损等癌细胞共同弱点的战略差异。为了更好地模拟不同表型和功能状态的癌细胞亚群,我们开发了一种二维培养(2D)、I 型胶原蛋白 3D 培养(3D)和干细胞类球体培养(类球体)的示意图组合,命名为 2D/3D/类球体方案。我们研究了肿瘤抑制因子 maspin 如何限制癌细跑的可塑性,并影响它们对不同机制药物的上下文相关反应,包括多西他赛、组蛋白去乙酰化酶(HDAC)抑制剂 MS-275 和离子载体抗生素盐霉素。我们表明,肿瘤细胞表型可塑性不是癌症干细胞所特有的属性。尽管如此,通过 2D/3D/类球体方案富集的三种前列腺癌细胞亚群表现出不同的药物反应。有趣的是,盐霉素是唯一能够有效杀死所有三种癌细胞亚群的药物,而不管它们的干性能力如何。此外,2D/3D/类球体方案可能是一种有用的模型,可以加速筛选有治愈潜力的癌症药物,同时避免对可能仅对某些但不是所有癌细胞亚群具有选择性毒性的化合物进行昂贵的特征描述。