Ayah A Farhat, Yazan A Almahdi, Fatima Z Alshuhani, Besa Xhabija
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引用次数: 0
摘要
黑色素瘤源于产生色素的黑色素细胞,是一种侵袭性致命皮肤癌。尽管对其进行了广泛的研究,但其发展和转移机制仍不清楚。本研究通过数字全息显微镜、主成分分析(PCA)和 t 分布随机邻域嵌入(t-SNE),使用定量相位成像技术来识别正常黑色素细胞和 SK-MEL-28 黑色素瘤细胞之间的形态、光学和行为差异。我们的发现揭示了细胞形状、大小和内部组织的显著差异,SK-MEL-28 细胞显示出更大的大小可变性、更多的多边形形状和更高的光学厚度。相移参数和表面粗糙度分析强调了黑色素瘤细胞均匀且可预测的纹理。小提琴图突显了 SK-MEL-28 细胞动态多样的迁移,与黑色素细胞的局部迁移形成鲜明对比。相关矩阵的分层聚类进一步揭示了复杂的形态和光学关系。将无标记成像与稳健的分析方法相结合,可以加深对黑色素瘤侵袭行为的了解,支持靶向治疗,并突出黑色素瘤精确诊断和治疗的潜在生物标记物。
Morphological and Optical Profiling of Melanocytes and SK-MEL-28 Melanoma Cells Via Digital Holographic Microscopy and Quantitative Phase Imaging.
Melanoma, which originates from pigment-producing melanocytes, is an aggressive and deadly skin cancer. Despite extensive research, its mechanisms of progression and metastasis remain unclear. This study uses quantitative phase imaging via digital holographic microscopy, Principal Component Analysis (PCA), and t-distributed Stochastic Neighbor Embedding (t-SNE) to identify the morphological, optical, and behavioral differences between normal melanocytes and SK-MEL-28 melanoma cells. Our findings reveal significant differences in cell shape, size, and internal organization, with SK-MEL-28 cells displaying greater size variability, more polygonal shapes, and higher optical thickness. Phase shift parameters and surface roughness analyses underscore melanoma cells' uniform and predictable textures. Violin plots highlight the dynamic and varied migration of SK-MEL-28 cells, contrasting with the localized movement of melanocytes. Hierarchical clustering of correlation matrices provides further insights into complex morphological and optical relationships. Integrating label-free imaging with robust analytical methods enhances understanding of melanoma's aggressive behavior, supporting targeted therapies and highlighting potential biomarkers for precise melanoma diagnostics and treatment.