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首页> 外文期刊>Science Advances >Minimal dosing of leukocyte targeting TRAIL decreases triple-negative breast cancer metastasis following tumor resection
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Minimal dosing of leukocyte targeting TRAIL decreases triple-negative breast cancer metastasis following tumor resection

机译:靶向TRAIL的白细胞剂量最少,可减少肿瘤切除后三阴性乳腺癌的转移

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Surgical removal of the primary tumor is a common practice in breast cancer treatment. However, postsurgical metastasis poses an immense setback in cancer therapy. Considering that 90% of cancer-related deaths are due to metastasis, antimetastatic therapeutic strategies that can target disseminating tumor cells in the circulation before they can form secondary tumors hold preclinical and clinical potential for cancer patients. Our current work uses a liposomal formulation functionalized with the adhesion receptor E-selectin and the apoptosis-inducing ligand TNF (tumor necrosis factor)–related apoptosis-inducing ligand (TRAIL) to reduce metastasis following tumor resection in an aggressive triple-negative breast cancer (TNBC) mouse model. We demonstrate that minimal administration of E-selectin–TRAIL liposomes can target metastasis in a TNBC model, with primary tumor resection to mimic clinical settings. Our study indicates that TRAIL liposomes, alone or in combination with existing clinically approved therapies, may neutralize distant metastasis of a broad range of tumor types systemically.
机译:外科手术切除原发性肿瘤是乳腺癌治疗中的普遍做法。然而,术后转移在癌症治疗中造成了巨大的挫折。考虑到90%的癌症相关死亡是由于转移引起的,可以在肿瘤形成继发性肿瘤之前在循环中扩散肿瘤细胞的抗转移治疗策略对癌症患者具有临床前和临床潜力。我们当前的工作使用脂质体制剂,该脂质体制剂具有粘附受体E-选择蛋白和凋亡诱导配体TNF(肿瘤坏死因子)相关的凋亡诱导配体(TRAIL)功能化,以减少侵袭性三阴性乳腺癌肿瘤切除后的转移。 (TNBC)鼠标模型。我们证明E-选择蛋白-TRAIL脂质体的最低限度给药可以靶向TNBC模型中的转移,并通过原发肿瘤切除来模拟临床环境。我们的研究表明,TRAIL脂质体单独或与现有临床批准的疗法联合使用,可能会全身性中和多种肿瘤的远处转移。

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