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通过靶向B7-H3的超声分子成像检测乳腺癌

Breast Cancer Detection by B7-H3-Targeted Ultrasound Molecular Imaging.

作者信息

Bachawal Sunitha V, Jensen Kristin C, Wilson Katheryne E, Tian Lu, Lutz Amelie M, Willmann Jürgen K

机构信息

Department of Radiology, Molecular Imaging Program at Stanford, Stanford University School of Medicine, Stanford, California.

Department of Pathology, Stanford University, Stanford, California. Veterans Affairs Palo Alto Health Care System, Palo Alto, California.

出版信息

Cancer Res. 2015 Jun 15;75(12):2501-9. doi: 10.1158/0008-5472.CAN-14-3361. Epub 2015 Apr 21.

Abstract

Ultrasound complements mammography as an imaging modality for breast cancer detection, especially in patients with dense breast tissue, but its utility is limited by low diagnostic accuracy. One emerging molecular tool to address this limitation involves contrast-enhanced ultrasound using microbubbles targeted to molecular signatures on tumor neovasculature. In this study, we illustrate how tumor vascular expression of B7-H3 (CD276), a member of the B7 family of ligands for T-cell coregulatory receptors, can be incorporated into an ultrasound method that can distinguish normal, benign, precursor, and malignant breast pathologies for diagnostic purposes. Through an IHC analysis of 248 human breast specimens, we found that vascular expression of B7-H3 was selectively and significantly higher in breast cancer tissues. B7-H3 immunostaining on blood vessels distinguished benign/precursors from malignant lesions with high diagnostic accuracy in human specimens. In a transgenic mouse model of cancer, the B7-H3-targeted ultrasound imaging signal was increased significantly in breast cancer tissues and highly correlated with ex vivo expression levels of B7-H3 on quantitative immunofluorescence. Our findings offer a preclinical proof of concept for the use of B7-H3-targeted ultrasound molecular imaging as a tool to improve the diagnostic accuracy of breast cancer detection in patients.

摘要

超声作为一种乳腺癌检测的成像方式,可补充乳腺X线摄影,尤其对于乳腺组织致密的患者,但它的效用因诊断准确性低而受到限制。一种新兴的分子工具来解决这一局限性,涉及使用靶向肿瘤新生血管分子特征的微泡的超声造影。在本研究中,我们阐述了如何将T细胞共调节受体B7配体家族成员B7-H3(CD276)的肿瘤血管表达纳入一种超声方法,该方法可区分正常、良性、癌前和恶性乳腺病变以用于诊断目的。通过对248例人类乳腺标本的免疫组化分析,我们发现B7-H3的血管表达在乳腺癌组织中选择性且显著更高。在人类标本中,血管上的B7-H3免疫染色以高诊断准确性区分良性/癌前病变与恶性病变。在癌症转基因小鼠模型中,B7-H3靶向超声成像信号在乳腺癌组织中显著增加,并且与定量免疫荧光上B7-H3的体外表达水平高度相关。我们的研究结果为使用B7-H3靶向超声分子成像作为提高患者乳腺癌检测诊断准确性的工具提供了临床前概念验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7276/4470725/89a676a892ab/nihms684458f1.jpg

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Breast Cancer Detection by B7-H3-Targeted Ultrasound Molecular Imaging.通过靶向B7-H3的超声分子成像检测乳腺癌
Cancer Res. 2015 Jun 15;75(12):2501-9. doi: 10.1158/0008-5472.CAN-14-3361. Epub 2015 Apr 21.

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