HER2阳性乳腺癌的综合化疗-免疫-放射治疗结合潜在microrna的回顾和亚太赫兹振动光谱的实验结果分析

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摘要

在这篇论文中,我们通过对NIH批准的治疗HER2阳性乳腺癌的综合分析,提出了一项乳腺癌研究的结果。本研究结合了亚太赫兹光谱的应用,通过测量唾液来可视化血液中循环的分子,从而分析微rna的参与。紫杉醇-通用名-紫杉醇(PT-J9267)联合曲妥珠单抗- anns0 /0和KadcylaTM(遗传名ado -曲妥珠单抗- Emtansine)在化疗和免疫治疗后进行放射治疗的3期联合治疗。使用PT的目的是阻止疾病扩散到乳房以外的其他器官和腋下淋巴结,以及缩小肿瘤的大小,以便于手术和放射学继续治疗。曲妥珠单抗(TZ)在第二步加入PT以防止化疗耐药的发展。静脉输注Kadcyla主要用于预防转移。基于文献综述和亚太赫兹振动光谱测量,使用Vibratess光谱仪对每次治疗前后每周采集的样品的吸收光谱进行了microRNA参与的综合分析。亚太赫兹光谱学在这项工作中的结果表明,在疾病发展和治疗过程的初始步骤之后,患者样本的光谱特征发生了戏剧性的变化。这些变化反映了最初参与的microrna数量的深度全局调控(减少)以及参与光谱的microrna的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrative chemo-immune-radiological treatment of HER2 positive breast cancer combined with a review of potential microRNAs involved and analysis of experimental results from sub-THz vibrational spectroscopy
In this paper we present the results of a Breast Cancer study by integrative analysis of a NIH approved treatment for HER2 positive breast cancer. This study is combined with analysis of Micro-RNA involvement from application of sub-THz spectroscopy for visualization of molecules circulating in blood by measuring saliva. The combination of Taxol-Generic Name-Paclitaxel (PT-J9267) and Trastuzumab-ANNS 0/0 and KadcylaTM (Genetic Name Ado-Trastuzumab Emtansine) were used in 3-stages of combined chemotherapeutic and immune-treatments followed by Radiation treatment. The goal of using PT was to stop spread of the disease to other organs outside of the breast and under arm lymph nodes, as well as to shrink the size of the tumor to facilitate surgery and radiology in continuation of the treatment. Trastuzumab (TZ) was added to PT in the 2nd step to prevent the development of chemoresistance. Intravenous infusion of Kadcyla was used mainly to prevent metastasis. Integrative analysis of microRNA participation was conducted based on literature review and sub-Terahertz vibrational spectroscopy measurements of absorption spectra from samples taken weekly before and after each treatment, using Vibratess’ spectrometer. The results from sub-THz spectroscopy in this work demonstrate dramatical modification of spectroscopic signatures from patient samples following disease development and the initial steps in the course of treatment. These changes reflect the deep global regulation (reduction) of the initially participating microRNAs amounts and changes in the microRNAs contributing to the spectra.
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