Burke Kathleen A, Dawes Ryan P, Cheema Mehar K, Van Hove Amy, Benoit Danielle S W, Perry Seth W, Brown Edward
University of Rochester, Department of Biomedical Engineering, 207 Robert B. Goergen Hall, P.O. Box 270168, Rochester, New York 14627, United States.
University of Rochester, Department of Neurobiology and Anatomy, 601 Elmwood Avenue, Rochester, New York 14642, United States.
J Biomed Opt. 2015 May;20(5):051024. doi: 10.1117/1.JBO.20.5.051024.
Second-harmonic generation (SHG) allows for the analysis of tumor collagen structural changes throughout metastatic progression. SHG directionality, measured through the ratio of the forward-propagating to backward-propagating signal (F/B ratio), is affected by collagen fibril diameter, spacing, and disorder of fibril packing within a fiber. As tumors progress, these parameters evolve, producing concurrent changes in F/B. It has been recently shown that the F/B of highly metastatic invasive ductal carcinoma (IDC) breast tumors is significantly different from less metastatic tumors. This suggests a possible relationship between the microstructure of collagen, as measured by the F/B, and the ability of tumor cells to locomote through that collagen. Utilizing in vitro collagen gels of different F/B ratios, we explored the relationship between collagen microstructure and motility of tumor cells in a “clean” environment, free of the myriad cells, and signals found in in vivo. We found a significant relationship between F/B and the total distance traveled by the tumor cell, as well as both the average and maximum velocities of the cells. Consequently, one possible mechanism underlying the observed relationship between tumor F/B and metastatic output in IDC patient samples is a direct influence of collagen structure on tumor cell motility.
二次谐波产生(SHG)可用于分析肿瘤在转移进展过程中胶原蛋白结构的变化。通过向前传播信号与向后传播信号的比值(F/B比值)测量的SHG方向性,会受到胶原纤维直径、间距以及纤维内纤维束排列紊乱程度的影响。随着肿瘤进展,这些参数会发生变化,导致F/B同时改变。最近研究表明,高转移性浸润性导管癌(IDC)乳腺肿瘤的F/B与低转移性肿瘤显著不同。这表明,通过F/B测量的胶原蛋白微观结构与肿瘤细胞在该胶原蛋白中移动的能力之间可能存在关联。利用具有不同F/B比值的体外胶原凝胶,我们在一个没有体内存在的大量细胞和信号的“纯净”环境中,探索了胶原微观结构与肿瘤细胞运动性之间的关系。我们发现F/B与肿瘤细胞的总移动距离以及细胞的平均速度和最大速度之间存在显著关联。因此,在IDC患者样本中观察到的肿瘤F/B与转移输出之间关系的一种可能机制是胶原蛋白结构对肿瘤细胞运动性的直接影响。