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靶向微泡在胰腺癌诊断分子成像中的研究现状

Current status of targeted microbubbles in diagnostic molecular imaging of pancreatic cancer.

作者信息

Jugniot Natacha, Bam Rakesh, Meuillet Emmanuelle J, Unger Evan C, Paulmurugan Ramasamy

机构信息

Department of Radiology Molecular Imaging Program at Stanford, Stanford University Palo Alto California USA.

NuvOx Pharma Tucson Arizona USA.

出版信息

Bioeng Transl Med. 2020 Sep 7;6(1):e10183. doi: 10.1002/btm2.10183. eCollection 2021 Jan.

DOI:10.1002/btm2.10183
PMID:33532585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7823123/
Abstract

Pancreatic ductal adenocarcinoma (PDAC) is often associated with a poor prognosis due to silent onset, resistance to therapies, and rapid spreading. Most patients are ineligible for curable surgery as they present with advanced disease at the time of diagnosis. Present diagnostic methods relying on anatomical changes have various limitations including difficulty to discriminate between benign and malignant conditions, invasiveness, the ambiguity of imaging results, or the inability to detect molecular biomarkers of PDAC initiation and progression. Therefore, new imaging technologies with high sensitivity and specificity are critically needed for accurately detecting PDAC and noninvasively characterizing molecular features driving its pathogenesis. Contrast enhanced targeted ultrasound (CETUS) is an upcoming molecular imaging modality that specifically addresses these issues. Unlike anatomical imaging modalities such as CT and MRI, molecular imaging using CETUS is promising for early and accurate detection of PDAC. The use of molecularly targeted microbubbles that bind to neovascular targets can enhance the ultrasound signal specifically from malignant PDAC tissues. This review discusses the current state of diagnostic imaging modalities for pancreatic cancer and places a special focus on ultrasound targeted-microbubble technology together with its clinical translatability for PDAC detection.

摘要

胰腺导管腺癌(PDAC)由于发病隐匿、对治疗耐药且扩散迅速,往往预后较差。大多数患者在诊断时已处于疾病晚期,不适合进行可治愈的手术。目前依赖解剖结构变化的诊断方法存在各种局限性,包括难以区分良性和恶性情况、具有侵入性、成像结果不明确,或无法检测出PDAC发生和发展的分子生物标志物。因此,迫切需要具有高灵敏度和特异性的新型成像技术,以准确检测PDAC并无创地表征驱动其发病机制的分子特征。对比增强靶向超声(CETUS)是一种新兴的分子成像模式,专门针对这些问题。与CT和MRI等解剖成像模式不同,使用CETUS的分子成像有望早期准确检测PDAC。使用与新生血管靶点结合的分子靶向微泡可以特异性增强来自恶性PDAC组织的超声信号。本综述讨论了胰腺癌诊断成像模式的现状,并特别关注超声靶向微泡技术及其在PDAC检测中的临床可转化性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a7/7823123/4312c666be46/BTM2-6-e10183-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a7/7823123/2917775a238d/BTM2-6-e10183-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a7/7823123/6b947377f764/BTM2-6-e10183-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a7/7823123/4312c666be46/BTM2-6-e10183-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a7/7823123/2917775a238d/BTM2-6-e10183-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a7/7823123/6b947377f764/BTM2-6-e10183-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a7/7823123/4312c666be46/BTM2-6-e10183-g003.jpg

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