Speirs Monique M P, Swensen Adam C, Chan Tsz Y, Jones Peter M, Holman John C, Harris McCall B, Maschek John A, Cox James E, Carson Richard H, Hill Jonathon T, Andersen Joshua L, Prince John T, Price John C
Department of Chemistry and Biochemistry, Brigham Young University, Provo, Utah, USA.
Health Sciences Cores-Metabolomics, University of Utah, Salt Lake, Utah, USA.
Oncotarget. 2019 Jan 11;10(4):449-479. doi: 10.18632/oncotarget.26533.
Tumor heterogeneity may arise through genetic drift and environmentally driven clonal selection for metabolic fitness. This would promote subpopulations derived from single cancer cells that exhibit distinct phenotypes while conserving vital pro-survival pathways. We aimed to identify significant drivers of cell fitness in pancreatic adenocarcinoma (PDAC) creating subclones in different nutrient formulations to encourage differential metabolic reprogramming. The genetic and phenotypic expression profiles of each subclone were analyzed relative to a healthy control cell line (hTert-HPNE). The subclones exhibited distinct variations in protein expression and lipid metabolism. Relative to hTert-HPNE, PSN-1 subclones uniformly maintained modified sphingolipid signaling and specifically retained elevated sphingosine-1-phosphate (S1P) relative to C16 ceramide (C16 Cer) ratios. Each clone utilized a different perturbation to this pathway, but maintained this modified signaling to preserve cancerous phenotypes, such as rapid proliferation and defense against mitochondria-mediated apoptosis. Although the subclones were unique in their sensitivity, inhibition of S1P synthesis significantly reduced the ratio of S1P/C16 Cer, slowed cell proliferation, and enhanced sensitivity to apoptotic signals. This reliance on S1P signaling identifies this pathway as a promising drug-sensitizing target that may be used to eliminate cancerous cells consistently across uniquely reprogrammed PDAC clones.
肿瘤异质性可能通过遗传漂变以及环境驱动的代谢适应性克隆选择而产生。这将促进源自单个癌细胞的亚群出现,这些亚群表现出不同的表型,同时保留重要的促生存途径。我们旨在确定胰腺腺癌(PDAC)中细胞适应性的重要驱动因素,通过在不同营养配方中创建亚克隆来促进不同的代谢重编程。相对于健康对照细胞系(hTert-HPNE),分析了每个亚克隆的基因和表型表达谱。这些亚克隆在蛋白质表达和脂质代谢方面表现出明显差异。相对于hTert-HPNE,PSN-1亚克隆一致地维持了修饰的鞘脂信号传导,并且相对于C16神经酰胺(C16 Cer)比率,特异性地保持了升高的鞘氨醇-1-磷酸(S1P)水平。每个克隆对该途径采用了不同的扰动,但维持这种修饰的信号传导以保留癌性表型,例如快速增殖和抵抗线粒体介导的凋亡。尽管这些亚克隆在敏感性方面是独特的,但抑制S1P合成显著降低了S1P/C16 Cer的比率,减缓了细胞增殖,并增强了对凋亡信号的敏感性。对S1P信号传导的这种依赖性将该途径确定为一个有前景的药物增敏靶点,可用于在独特重编程的PDAC克隆中一致地消除癌细胞。