Bachawal Sunitha, Bean Gregory R, Krings Gregor, Wilson Katheryne E
1Department of Radiology, Molecular Imaging Program at Stanford, Stanford University, School of Medicine, Stanford, CA USA.
2Department of Pathology, Stanford University, School of Medicine, Stanford, CA USA.
NPJ Breast Cancer. 2020 Apr 29;6:14. doi: 10.1038/s41523-020-0158-y. eCollection 2020.
Ductal carcinoma in situ (DCIS) will account for 62,930 cases of breast cancer in 2019. DCIS is a pre-invasive lesion which may not progress to invasive carcinoma, yet surgery remains the mainstay treatment. Molecular imaging of a specific marker for DCIS grade for detection and active surveillance are critically needed to reduce potential overtreatment. First, breast cancer marker B7-H3 (CD276) expression was evaluated by immunohistochemical staining in 123 human specimens including benign epithelium (H-score 10.0 ± 8.2) and low (20.8 ± 17.7), intermediate (87.1 ± 69.5), and high (159.1 ± 87.6) grade DCIS, showing a positive association with DCIS nuclear grade ( < 0.001, AUC 0.96). Next, a murine DCIS model was combined with ultrasound molecular imaging of B7-H3 targeted microbubbles to differentiate normal glands from those harboring DCIS ( = 100, FVB/N-Tg(MMTVPyMT)634Mul, AUC 0.89). Finally, photoacoustic and fluorescence molecular imaging with an anti-B7-H3 antibody-indocyanine green conjugate were utilized for DCIS detection ( = 53). Molecular imaging of B7-H3 expression may allow for active surveillance of DCIS.
2019年,导管原位癌(DCIS)将占乳腺癌病例62930例。DCIS是一种非侵袭性病变,可能不会发展为浸润性癌,但手术仍是主要治疗方法。迫切需要对DCIS分级的特异性标志物进行分子成像,以用于检测和主动监测,从而减少潜在的过度治疗。首先,通过免疫组织化学染色在123例人体标本中评估乳腺癌标志物B7-H3(CD276)的表达,这些标本包括良性上皮(H评分10.0±8.2)以及低级别(20.8±17.7)、中级(87.1±69.5)和高级别(159.1±87.6)的DCIS,结果显示其与DCIS核分级呈正相关(<0.001,曲线下面积0.96)。接下来,将小鼠DCIS模型与靶向B7-H3的微泡超声分子成像相结合,以区分正常腺体和患有DCIS的腺体(n = 100,FVB/N-Tg(MMTVPyMT)634Mul,曲线下面积0.89)。最后,利用抗B7-H3抗体-吲哚菁绿偶联物进行光声和荧光分子成像以检测DCIS(n = 53)。B7-H3表达的分子成像可能有助于对DCIS进行主动监测。