Division of Pharmacoengineering and Molecular Pharmaceutics and Center for Nanotechnology in Drug Delivery, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Small. 2019 Mar;15(9):e1805182. doi: 10.1002/smll.201805182. Epub 2019 Jan 28.
Triple negative breast cancer (TNBC) is the most aggressive breast cancer subtype. Currently, no targeted treatment is available for TNBC, and the most common clinical therapy is tumor resection, which often promotes metastasis risks. Strong evidence suggests that the lymphatic metastasis is mediated by the C-C chemokine receptor type 7 (CCR7)/C-C motif chemokine ligand 21 crosstalk between tumor cells and the lymphatic system. It is hypothesized that CCR7 is a key immune modulator in the tumor microenvironment and the local blockade of CCR7 could effectively inhibit TNBC lymphatic metastasis. Accordingly, a plasmid encoding an antagonistic CCR7 affinity protein-CCR7 trap is delivered by tumor targeting nanoparticles in a highly metastatic 4T1 TNBC mouse model. Results show that CCR7 traps are transiently expressed, locally disrupt the signaling pathways in the tumor site, and efficiently inhibit TNBC lymphatic metastasis, without inducing immunosuppression as observed in systemic therapies using CCR7 monoclonal antibody. Significantly, upon applying CCR7 trap therapy prior to tumor resection, a 4T1 TNBC mouse model shows good prognosis without any further metastasis and relapse. In addition, CCR7 trap therapy efficiently inhibits the lymphatic metastasis in a B16F10 melanoma mouse model, indicating its great potential for various metastatic diseases treatment.
三阴性乳腺癌(TNBC)是最具侵袭性的乳腺癌亚型。目前,针对 TNBC 尚无靶向治疗方法,最常见的临床治疗方法是肿瘤切除术,这往往会增加转移风险。有强有力的证据表明,淋巴转移是由肿瘤细胞与淋巴系统之间的 C-C 趋化因子受体 7(CCR7)/C-C 基序趋化因子配体 21 相互作用介导的。假设 CCR7 是肿瘤微环境中的关键免疫调节剂,局部阻断 CCR7 可以有效抑制 TNBC 的淋巴转移。因此,在高转移性 4T1 TNBC 小鼠模型中,通过肿瘤靶向纳米颗粒递送来编码拮抗 CCR7 亲和力蛋白-CCR7 陷阱的质粒。结果表明,CCR7 陷阱是瞬时表达的,局部破坏肿瘤部位的信号通路,并有效地抑制 TNBC 的淋巴转移,而不会像使用 CCR7 单克隆抗体进行全身治疗那样引起免疫抑制。值得注意的是,在肿瘤切除前应用 CCR7 陷阱治疗,4T1 TNBC 小鼠模型显示出良好的预后,没有进一步的转移和复发。此外,CCR7 陷阱治疗有效地抑制了 B16F10 黑色素瘤小鼠模型中的淋巴转移,表明其在治疗各种转移性疾病方面具有巨大潜力。