Weygant Nathaniel, Ge Yang, Qu Dongfeng, Kaddis John S, Berry William L, May Randal, Chandrakesan Parthasarathy, Bannerman-Menson Edwin, Vega Kenneth J, Tomasek James J, Bronze Michael S, An Guangyu, Houchen Courtney W
The University of Oklahoma Health Sciences Center Department of Medicine, Oklahoma City, Oklahoma.
Beijing Chao-Yang Hospital Department of Oncology, Capital Medical University, Beijing, China.
Cancer Res. 2016 Jul 15;76(14):4090-9. doi: 10.1158/0008-5472.CAN-16-0029. Epub 2016 Jun 10.
Doublecortin-like kinase 1 (DCLK1) is a gastrointestinal (GI) tuft cell kinase that has been investigated as a biomarker of cancer stem-like cells in colon and pancreatic cancers. However, its utility as a biomarker may be limited in principle by signal instability and dilution in heterogeneous tumors, where the proliferation of diverse tumor cell lineages obscures the direct measurement of DCLK1 activity. To address this issue, we explored the definition of a miRNA signature as a surrogate biomarker for DCLK1 in cancer stem-like cells. Utilizing RNA/miRNA-sequencing datasets from the Cancer Genome Atlas, we identified a surrogate 15-miRNA expression signature for DCLK1 activity across several GI cancers, including colon, pancreatic, and stomach cancers. Notably, Cox regression and Kaplan-Meier analysis demonstrated that this signature could predict the survival of patients with these cancers. Moreover, we identified patient subgroups that predicted the clinical utility of this DCLK1 surrogate biomarker. Our findings greatly strengthen the clinical significance for DCLK1 expression across GI cancers. Further, they provide an initial guidepost toward the development of improved prognostic biomarkers or companion biomarkers for DCLK1-targeted therapies to eradicate cancer stem-like cells in these malignancies. Cancer Res; 76(14); 4090-9. ©2016 AACR.
双皮质素样激酶1(DCLK1)是一种胃肠道(GI)簇状细胞激酶,已被研究作为结肠癌和胰腺癌中癌症干细胞样细胞的生物标志物。然而,其作为生物标志物的效用在原则上可能受到异质性肿瘤中信号不稳定性和稀释的限制,在这些肿瘤中,不同肿瘤细胞谱系的增殖掩盖了DCLK1活性的直接测量。为了解决这个问题,我们探索了一种miRNA特征的定义,作为癌症干细胞样细胞中DCLK1的替代生物标志物。利用来自癌症基因组图谱的RNA/miRNA测序数据集,我们在包括结肠癌、胰腺癌和胃癌在内的几种胃肠道癌症中确定了一个用于DCLK1活性的替代15-miRNA表达特征。值得注意的是,Cox回归和Kaplan-Meier分析表明,这个特征可以预测这些癌症患者的生存情况。此外,我们确定了预测这种DCLK1替代生物标志物临床效用的患者亚组。我们的发现极大地加强了DCLK1在胃肠道癌症中表达的临床意义。此外,它们为开发改进的预后生物标志物或伴随生物标志物提供了初步指导,以用于靶向DCLK1的疗法来根除这些恶性肿瘤中的癌症干细胞样细胞。《癌症研究》;76(14);4090 - 4099。©2016美国癌症研究协会。