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一种新型曲妥珠单抗缀合物的合成及其与紫杉醇和锆整合用于HER2阳性乳腺癌诊疗应用的可行性评估

Synthesis and Feasibility Evaluation of a new Trastuzumab Conjugate Integrated with Paclitaxel and Zr for Theranostic Application Against HER2-Expressing Breast Cancers.

作者信息

Jang Joo Hee, Han Sang Jin, Kim Jung Young, Kim Kwang Il, Lee Kyo Chul, Kang Chi Soo

机构信息

Division of Applied RI Korea Institute of Radiological and Medical Sciences 75 Nowon-ro, Nowon-gu Seoul Korea 01812.

出版信息

ChemistryOpen. 2019 Apr 8;8(4):451-456. doi: 10.1002/open.201900037. eCollection 2019 Apr.

Abstract

The preparation and   evaluation of a theranostic conjugate composed of trastuzumab, paclitaxel (PTX), and deferoxamine (DFO)-chelated Zr have been reported. These comounds have potential applications against HER2 receptor positive breast cancers. We conjugated DFO and PTX to trastuzumab by exploiting simple conjugation chemistry. The conjugate (DFO-trastuzumab-PTX) showed excellent radiolabeling efficiency with Zr and the labeled conjugate had high in vitro stability in human serum. Furthermore, DFO-trastuzumab-PTX displayed comparable cytotoxicity with PTX and Zr-DFO-trastuzumab-PTX exhibited HER2 receptor-mediated binding on HER2-positive MDA-MB-231 breast cancer cells. The results of our in vitro study indicate high potential of Zr-DFO-trastuzumab-PTX to be utilized in the theranostic application against HER2-postive breast cancers.

摘要

已报道了由曲妥珠单抗、紫杉醇(PTX)和去铁胺(DFO)螯合的锆组成的诊疗共轭物的制备和评估。这些化合物在抗HER2受体阳性乳腺癌方面具有潜在应用。我们通过利用简单的共轭化学方法将DFO和PTX与曲妥珠单抗共轭。该共轭物(DFO-曲妥珠单抗-PTX)显示出与锆具有优异的放射性标记效率,且标记后的共轭物在人血清中具有较高的体外稳定性。此外,DFO-曲妥珠单抗-PTX表现出与PTX相当的细胞毒性,而Zr-DFO-曲妥珠单抗-PTX在HER2阳性的MDA-MB-231乳腺癌细胞上表现出HER2受体介导的结合。我们的体外研究结果表明,Zr-DFO-曲妥珠单抗-PTX在针对HER2阳性乳腺癌的诊疗应用中具有很高的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d17/6454217/f63f018060b3/OPEN-8-451-g003.jpg

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