Ma Xin, Botros Andro, Yun Sylvia R, Park Eun Young, Kim Olga, Park Soojin, Pham Thu-Huyen, Chen Ruihong, Palaniappan Murugesan, Matzuk Martin M, Kim Jaeyeon, Fernández Facundo M
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA, United States.
Departments of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN, United States.
Front Chem. 2024 Jan 8;11:1332816. doi: 10.3389/fchem.2023.1332816. eCollection 2023.
No effective screening tools for ovarian cancer (OC) exist, making it one of the deadliest cancers among women. Considering that little is known about the detailed progression and metastasis mechanism of OC at a molecular level, it is crucial to gain more insights into how metabolic and signaling alterations accompany its development. Herein, we present a comprehensive study using ultra-high-resolution Fourier transform ion cyclotron resonance matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) to investigate the spatial distribution and alterations of lipids in ovarian tissues collected from double knockout ( = 4) and triple mutant mouse models ( = 4) of high-grade serous ovarian cancer (HGSOC). Lipids belonging to a total of 15 different classes were annotated and their abundance changes were compared to those in healthy mouse reproductive tissue ( = 4), mapping onto major lipid pathways involved in OC progression. From intermediate-stage OC to advanced HGSC, we provide direct visualization of lipid distributions and their biological links to inflammatory response, cellular stress, cell proliferation, and other processes. We also show the ability to distinguish tumors at different stages from healthy tissues via a number of highly specific lipid biomarkers, providing targets for future panels that could be useful in diagnosis.
目前尚无有效的卵巢癌(OC)筛查工具,这使其成为女性中最致命的癌症之一。鉴于在分子水平上对OC的详细进展和转移机制了解甚少,深入了解代谢和信号改变如何伴随其发展至关重要。在此,我们进行了一项全面的研究,使用超高分辨率傅里叶变换离子回旋共振基质辅助激光解吸/电离(MALDI)质谱成像(MSI)来研究从高级别浆液性卵巢癌(HGSOC)的双敲除(n = 4)和三突变小鼠模型(n = 4)收集的卵巢组织中脂质的空间分布和变化。共注释了15种不同类别的脂质,并将它们的丰度变化与健康小鼠生殖组织(n = 4)中的丰度变化进行比较,绘制到参与OC进展的主要脂质途径上。从中间阶段的OC到晚期HGSC,我们提供了脂质分布及其与炎症反应、细胞应激、细胞增殖和其他过程的生物学联系的直接可视化。我们还展示了通过一些高度特异性的脂质生物标志物区分不同阶段肿瘤与健康组织的能力,为未来可能用于诊断的检测组合提供了靶点。