Sub-terahertz vibrational spectroscopy of ovarian cancer and normal control tissue for molecular diagnostic technology.

IF 1.9
Tatiana Globus, Christopher Moskaluk, Patcharin Pramoonjago, Boris Gelmont, Aaron Moyer, Alexei Bykhovski, Jerome Ferrance
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引用次数: 5

Abstract

We introduce here recently developed highly resolved Sub-Terahertz resonance spectroscopy of biological molecules and cells combined with molecular dynamics (MD) computational analysis as a new approach for optical visualization and quantification of the presence of microRNAs, particularly the mir-200 family, as potential biomarkers in samples from tissue of epithelial ovarian cancers for disease early detection, analysis, prognosis and treatment.METHOD: A set of samples for this study was prepared from anonymized archival formalin-fixed, paraffin-embedded ovarian epithelial tissue containing regions of invasive neoplastic cells from cases of high-histologic grade serous papillary ovarian carcinoma. Control samples were normal mucosa from fallopian tubes of patients with no known malignancy. Spectroscopic characterization of tissue samples in this study was performed using a continuous wave, frequency domain automated spectrometer operating at room temperature in the spectral region of 310-500 GHz. The spectral results were compared with molecular dynamics simulations and absorption coefficient calculations utilized to predict the absorption spectra.RESULTS: The characteristic spectroscopic features in absorption spectra, particularly the presence of absorption peaks near 13 cm-1 have been identified as cancer indicators. Tissue samples heterogeneity, reflected by diverse spectral signatures, provides additional, very specific information that may be used for identification of cancer subtypes, clinical behavior or sensitivity to specific therapies. Further work is warranted to determine if this signature can be detected in bio-fluids from ovarian cancer patients. If strongly correlated with cancer burden, it may then be investigated as a potential new biomarker for disease monitoring, and also perhaps as a biomarker for cancer screening.

卵巢癌和正常对照组织的亚太赫兹振动光谱分子诊断技术。
我们在此介绍最近开发的生物分子和细胞的高分辨率亚太赫兹共振光谱结合分子动力学(MD)计算分析,作为一种光学可视化和定量microrna存在的新方法,特别是mir-200家族,作为上皮性卵巢癌组织样本中潜在的生物标志物,用于疾病的早期检测、分析、预后和治疗。方法:本研究的一组样本来自匿名档案福尔马林固定,石蜡包埋的卵巢上皮组织,其中包含来自高组织学级别浆液性乳头状卵巢癌的侵袭性肿瘤细胞区域。对照标本为未见恶性肿瘤患者输卵管正常黏膜。本研究中组织样品的光谱表征使用室温下310-500 GHz光谱区域的连续波频域自动光谱仪进行。光谱结果与分子动力学模拟和用于预测吸收光谱的吸收系数计算进行了比较。结果:吸收光谱中的特征光谱特征,特别是13 cm-1附近的吸收峰的存在已被确定为癌症指标。不同光谱特征反映的组织样本异质性提供了额外的、非常具体的信息,可用于识别癌症亚型、临床行为或对特定治疗的敏感性。需要进一步的工作来确定这种特征是否可以在卵巢癌患者的生物体液中检测到。如果与癌症负担密切相关,那么它可能会被研究作为疾病监测的潜在新生物标志物,也可能作为癌症筛查的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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