Department of Mathematics and Statistics, Georgia State University, Atlanta, GA, USA.
Cancer Biology Graduate Program, Emory University, Atlanta, GA, USA.
Sci Rep. 2017 Jan 3;7:39498. doi: 10.1038/srep39498.
Invasive cancer cells interact with the surrounding extracellular matrix (ECM), remodeling ECM fiber network structure by condensing, degrading, and aligning these fibers. We developed a novel local alignment vector analysis method to quantitatively measure collagen fiber alignment as a vector field using Circular Statistics. This method was applied to human non-small cell lung carcinoma (NSCLC) cell lines, embedded as spheroids in a collagen gel. Collagen remodeling was monitored using second harmonic generation imaging under normal conditions and when the LKB1-MARK1 pathway was disrupted through RNAi-based approaches. The results showed that inhibiting LKB1 or MARK1 in NSCLC increases the collagen fiber alignment and captures outward alignment vectors from the tumor spheroid, corresponding to high invasiveness of LKB1 mutant cancer cells. With time-lapse imaging of ECM micro-fiber morphology, the local alignment vector can measure the dynamic signature of invasive cancer cell activity and cell-migration-induced ECM and collagen remodeling and realigning dynamics.
侵袭性癌细胞与周围细胞外基质(ECM)相互作用,通过凝聚、降解和排列这些纤维来重塑 ECM 纤维网络结构。我们开发了一种新的局部对齐向量分析方法,使用循环统计来定量测量胶原纤维的对齐方式作为一个向量场。该方法应用于人类非小细胞肺癌(NSCLC)细胞系,这些细胞系在胶原凝胶中被包裹成球体。在正常条件下和通过基于 RNAi 的方法破坏 LKB1-MARK1 通路时,使用二次谐波产生成像来监测胶原重塑。结果表明,抑制 NSCLC 中的 LKB1 或 MARK1 会增加胶原纤维的排列,并从肿瘤球体捕获向外的排列向量,这与 LKB1 突变癌细胞的高侵袭性相对应。通过对 ECM 微纤维形态的延时成像,局部对齐向量可以测量侵袭性癌细胞活性的动态特征以及细胞迁移诱导的 ECM 和胶原重塑和重新排列动力学。