Sans Marta, Gharpure Kshipra, Tibshirani Robert, Zhang Jialing, Liang Li, Liu Jinsong, Young Jonathan H, Dood Robert L, Sood Anil K, Eberlin Livia S
Department of Chemistry, The University of Texas at Austin, Austin, Texas.
Department of Gynecologic Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer Res. 2017 Jun 1;77(11):2903-2913. doi: 10.1158/0008-5472.CAN-16-3044. Epub 2017 Apr 17.
Ovarian high-grade serous carcinoma (HGSC) results in the highest mortality among gynecological cancers, developing rapidly and aggressively. Dissimilarly, serous borderline ovarian tumors (BOT) can progress into low-grade serous carcinomas and have relatively indolent clinical behavior. The underlying biological differences between HGSC and BOT call for accurate diagnostic methodologies and tailored treatment options, and identification of molecular markers of aggressiveness could provide valuable biochemical insights and improve disease management. Here, we used desorption electrospray ionization (DESI) mass spectrometry (MS) to image and chemically characterize the metabolic profiles of HGSC, BOT, and normal ovarian tissue samples. DESI-MS imaging enabled clear visualization of fine papillary branches in serous BOT and allowed for characterization of spatial features of tumor heterogeneity such as adjacent necrosis and stroma in HGSC. Predictive markers of cancer aggressiveness were identified, including various free fatty acids, metabolites, and complex lipids such as ceramides, glycerophosphoglycerols, cardiolipins, and glycerophosphocholines. Classification models built from a total of 89,826 individual pixels, acquired in positive and negative ion modes from 78 different tissue samples, enabled diagnosis and prediction of HGSC and all tumor samples in comparison with normal tissues, with overall agreements of 96.4% and 96.2%, respectively. HGSC and BOT discrimination was achieved with an overall accuracy of 93.0%. Interestingly, our classification model allowed identification of three BOT samples presenting unusual histologic features that could be associated with the development of low-grade carcinomas. Our results suggest DESI-MS as a powerful approach for rapid serous ovarian cancer diagnosis based on altered metabolic signatures. .
卵巢高级别浆液性癌(HGSC)在妇科癌症中死亡率最高,发展迅速且侵袭性强。与之不同的是,浆液性交界性卵巢肿瘤(BOT)可进展为低级别浆液性癌,临床行为相对惰性。HGSC和BOT之间潜在的生物学差异需要准确的诊断方法和个性化的治疗方案,而识别侵袭性分子标志物可为疾病管理提供有价值的生化见解并加以改善。在此,我们使用解吸电喷雾电离(DESI)质谱(MS)对HGSC、BOT和正常卵巢组织样本的代谢谱进行成像和化学表征。DESI-MS成像能够清晰显示浆液性BOT中的细乳头分支,并可表征肿瘤异质性的空间特征,如HGSC中的相邻坏死和基质。确定了癌症侵袭性的预测标志物,包括各种游离脂肪酸、代谢物以及复杂脂质,如神经酰胺、甘油磷酸甘油、心磷脂和甘油磷酸胆碱。从78个不同组织样本以正离子和负离子模式采集的总共89,826个单个像素构建的分类模型,能够与正常组织相比诊断和预测HGSC以及所有肿瘤样本,总体一致性分别为96.4%和96.2%。HGSC和BOT的鉴别总体准确率达到93.0%。有趣的是,我们的分类模型能够识别出三个具有异常组织学特征的BOT样本,这些特征可能与低级别癌的发生有关。我们的结果表明,DESI-MS是一种基于代谢特征改变快速诊断浆液性卵巢癌的强大方法。