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辐射增强对三阴性乳腺癌中富含半乳糖凝集素-1的恶性基质的治疗靶向作用。

Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer.

作者信息

Upreti Meenakshi, Jyoti Amar, Johnson Sara E, Swindell Elden P, Napier Dana, Sethi Pallavi, Chan Ryan, Feddock Jonathan M, Weiss Heidi L, O'Halloran Thomas V, Evers B Mark

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY, USA.

Department of Pathology, University of Kentucky, Lexington, KY, USA.

出版信息

Oncotarget. 2016 Jul 5;7(27):41559-41574. doi: 10.18632/oncotarget.9490.

Abstract

Currently there are no FDA approved targeted therapies for Triple Negative Breast Cancer (TNBC). Ongoing clinical trials for TNBC have focused primarily on targeting the epithelial cancer cells. However, targeted delivery of cytotoxic payloads to the non-transformed tumor associated-endothelium can prove to be an alternate approach that is currently unexplored. The present study is supported by recent findings on elevated expression of stromal galectin-1 in clinical samples of TNBC and our ongoing findings on stromal targeting of radiation induced galectin-1 by the anginex-conjugated arsenic-cisplatin loaded liposomes using a novel murine tumor model. We demonstrate inhibition of tumor growth and metastasis in response to the multimodal nanotherapeutic strategy using a TNBC model with orthotopic tumors originating from 3D tumor tissue analogs (TTA) comprised of tumor cells, endothelial cells and fibroblasts. The 'rigorous' combined treatment regimen of radiation and targeted liposomes is also shown to be well tolerated. More importantly, the results presented provide a means to exploit clinically relevant radiation dose for concurrent receptor mediated enhanced delivery of chemotherapy while limiting overall toxicity. The proposed study is significant as it falls in line with developing combinatorial therapeutic approaches for stroma-directed tumor targeting using tumor models that have an appropriate representation of the TNBC microenvironment.

摘要

目前,美国食品药品监督管理局(FDA)尚未批准用于三阴性乳腺癌(TNBC)的靶向疗法。正在进行的TNBC临床试验主要集中于靶向上皮癌细胞。然而,将细胞毒性药物有效载荷靶向递送至未转化的肿瘤相关内皮细胞可能是一种目前尚未探索的替代方法。本研究得到了TNBC临床样本中基质半乳糖凝集素-1表达升高的最新发现,以及我们正在进行的关于使用新型小鼠肿瘤模型,通过血管生成素缀合的负载砷-顺铂的脂质体对辐射诱导的半乳糖凝集素-1进行基质靶向的研究结果的支持。我们使用源自由肿瘤细胞、内皮细胞和成纤维细胞组成的3D肿瘤组织类似物(TTA)的原位肿瘤TNBC模型,证明了多模态纳米治疗策略对肿瘤生长和转移的抑制作用。放疗和靶向脂质体的“严格”联合治疗方案也显示出良好的耐受性。更重要的是,所呈现的结果提供了一种方法,可利用临床相关的辐射剂量,在限制总体毒性的同时,通过受体介导增强化疗药物的递送。拟议的研究具有重要意义,因为它符合使用能恰当呈现TNBC微环境的肿瘤模型,开发针对基质导向肿瘤靶向的联合治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/825f/5173078/1e3a134dd609/oncotarget-07-41559-g001.jpg

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