Université-Paris-Diderot, Sorbonne-Paris-Cité, Laboratoire Pathologie, UMR-S942, F-75010, Paris, France.
INSERM, U942, Paris, France.
J Exp Clin Cancer Res. 2019 Jul 12;38(1):306. doi: 10.1186/s13046-019-1305-x.
HER2-overexpressing metastatic breast cancers are challenging practice in oncology when they become resistant to anti-HER2 therapies such as trastuzumab. In these clinical situations, HER2-overexpression persists in metastatic localizations, and can thus be used for active targeting using innovative therapeutic approaches. Functionalized gold nanoparticles with anti-HER2 antibody can be stimulated by near-infrared light to induce hyperthermia.
Here, hybrid anti-HER2 gold nanoshells were engineered for photothermal therapy to overcome trastuzumab resistance in HER2-overexpressing breast cancer xenografts.
When gold nanoshells were administered in HER2-tumor xenografts, no toxicity was observed. A detailed pharmacokinetic study showed a time-dependent accumulation of gold nanoshells within the tumors, significantly greater with functionalized gold nanoshells at 72 h. This enabled us to optimize the treatment protocol and irradiate the mice when the anti-HER2 gold nanoshells had accumulated most in the tumors. After weekly injections of anti-HER2 gold nanoshells, and repeated irradiations with a femtosecond-pulsed laser over four weeks, tumor growth was significantly inhibited. Detailed tissue microscopic analyses showed that the tumor growth inhibition was due to an anti-angiogenic effect, coherent with a preferential distribution of the nanoshells in tumor microvessels. We also showed a direct tumor cell effect with apoptosis and inhibition of proliferation, coherent with an immune-mediated targeting of tumor cells by anti-HER2 nanoshells.
This preclinical study thus supports the use of anti-HER2 gold nanoshells and photothermal therapy to overcome trastuzumab resistance in HER2-overexpressing breast cancer.
当曲妥珠单抗等抗 HER2 治疗产生耐药性时,HER2 过表达转移性乳腺癌成为肿瘤学中的棘手问题。在这些临床情况下,HER2 过表达持续存在于转移性病灶中,因此可以使用创新的治疗方法进行主动靶向治疗。具有抗 HER2 抗体的功能化金纳米颗粒可以被近红外光刺激以诱导热疗。
在这里,设计了用于光热治疗的杂交抗 HER2 金纳米壳,以克服 HER2 过表达乳腺癌异种移植中的曲妥珠单抗耐药性。
当金纳米壳被给予 HER2 肿瘤异种移植时,没有观察到毒性。详细的药代动力学研究表明,金纳米壳在肿瘤内的积累具有时间依赖性,在 72 小时时,功能化金纳米壳的积累明显更大。这使我们能够优化治疗方案,并在抗 HER2 金纳米壳在肿瘤中积累最多时对小鼠进行照射。每周注射抗 HER2 金纳米壳,并用飞秒脉冲激光重复照射四周后,肿瘤生长明显受到抑制。详细的组织显微镜分析表明,肿瘤生长抑制是由于抗血管生成作用,与纳米壳在肿瘤微血管中的优先分布一致。我们还显示了凋亡和增殖抑制的直接肿瘤细胞效应,与抗 HER2 纳米壳对肿瘤细胞的免疫介导靶向一致。
因此,这项临床前研究支持使用抗 HER2 金纳米壳和光热疗法来克服 HER2 过表达乳腺癌中的曲妥珠单抗耐药性。