Wu Zhihao, Shi Tao, Shao Qi, Chen Dongmei, Gao Peisheng, Wang Jie, Xu Ting, Meng Qingqing, Li Shaoshun
School of Pharmaceutical Sciences, Shanghai Jiao Tong University, Shanghai 200240, China.
The International Peace Maternal and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200030, China.
Mol Pharm. 2025 Mar 3;22(3):1507-1517. doi: 10.1021/acs.molpharmaceut.4c01223. Epub 2025 Jan 30.
Early detection and precise treatment for breast cancer are crucial, given its high global incidence rate. Hence, the development of novel imaging targets is essential for diagnosing and monitoring resistance to chemotherapy, which is pivotal for achieving precise and personalized treatment for breast cancer patients. In our previous work, we successfully developed a near-infrared (NIR) probe for CYP1B1-targeted imaging. In this study, we aimed to investigate the utility of the probe as a NIR fluorescence and photoacoustic dual-mode imaging probe for the detection and surveillance of breast cancer. Western blotting of cancer cell lines has confirmed that CYP1B1 is widely expressed in breast cancer and gynecological cancer. In vitro NIR fluorescence imaging capability of the probe for tracking CYP1B1-positive tumor cells was validated by using confocal microscopy. Further studies, including in vivo fluorescence and photoacoustic dual-model imaging and ex vivo biological distribution analysis on a triple-negative breast cancer xenograft mouse model, demonstrated that the probe selectively accumulated in tumor tissue within as early as 0.5 h postinjection. The results of the surgical resection experiment revealed that the tumor could be entirely removed under the guidance of NIR imaging, thereby indicating the probe's efficacy in surgical navigation. CYP1B1 expression was found to be upregulated in adriamycin (ADR)-resistant breast cancer cells, MCF-7/ADR. Consequently, the sensitivity of CYP1B1 overexpressed cells, MCF-7/1B1, to ADR was significantly reduced, with an IC value of 0.586 ± 0.0934 μM, compared to the parental MCF-7 cells with an IC value of 0.183 ± 0.0444 μM. In vivo and ex vivo imaging assays conducted on MCF-7/ADR tumor-bearing mice demonstrated that the probe was specifically enriched in tumor sites, suggesting its potential for monitoring chemotherapy resistance in breast cancer. This study expands the scope of application for NIR probe , establishing its utility in breast cancer diagnosis through fluorescence-photoacoustic dual-model imaging, monitoring of chemotherapy resistance, and guidance for surgical resection. This strategy paves the way for novel approaches to precise and personalized treatment for breast cancer patients.
鉴于乳腺癌在全球的高发病率,早期检测和精准治疗至关重要。因此,开发新型成像靶点对于诊断和监测化疗耐药性至关重要,这对于实现乳腺癌患者的精准和个性化治疗至关重要。在我们之前的工作中,我们成功开发了一种用于CYP1B1靶向成像的近红外(NIR)探针。在本研究中,我们旨在研究该探针作为近红外荧光和光声双模式成像探针在乳腺癌检测和监测中的效用。对癌细胞系进行的蛋白质免疫印迹分析证实,CYP1B1在乳腺癌和妇科癌症中广泛表达。通过共聚焦显微镜验证了该探针在体外追踪CYP1B1阳性肿瘤细胞的近红外荧光成像能力。进一步的研究,包括在三阴性乳腺癌异种移植小鼠模型上进行的体内荧光和光声双模式成像以及离体生物分布分析,表明该探针在注射后最早0.5小时内就选择性地在肿瘤组织中积累。手术切除实验结果显示,在近红外成像引导下肿瘤可以被完全切除,从而表明该探针在手术导航中的有效性。发现在阿霉素(ADR)耐药的乳腺癌细胞MCF-7/ADR中CYP1B1表达上调。因此,与亲本MCF-7细胞(IC值为0.183±0.0444μM)相比,CYP1B1过表达细胞MCF-7/1B1对ADR的敏感性显著降低,IC值为0.586±0.0934μM。对携带MCF-7/ADR肿瘤的小鼠进行的体内和离体成像分析表明,该探针在肿瘤部位特异性富集,表明其在监测乳腺癌化疗耐药性方面的潜力。本研究扩展了近红外探针的应用范围,确立了其在通过荧光-光声双模式成像进行乳腺癌诊断、监测化疗耐药性以及指导手术切除方面的效用。该策略为乳腺癌患者精准和个性化治疗的新方法铺平了道路。