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新型肿瘤归巢细胞穿透肽的设计与表征及其在 TGFBR3 高表达肿瘤中的药物递送

Design and characterization of a novel tumor-homing cell-penetrating peptide for drug delivery in TGFBR3 high-expressing tumors.

机构信息

Department of Applied Biology, East China University of Science and Technology, Shanghai, China.

ECUST-FONOW Joint Research Center for Innovative Medicines, East China University of Science and Technology, Shanghai, China.

出版信息

Chem Biol Drug Des. 2023 Dec;102(6):1421-1434. doi: 10.1111/cbdd.14333. Epub 2023 Aug 24.

Abstract

Targeted therapy has attracted more and more attention in cancer treatment in recent years. However, due to the diversity of tumor types and the mutation of target sites on the tumor surface, some existing targets are no longer suitable for tumor therapy. In addition, the long-term administration of a single targeted drug can also lead to drug resistance and attenuate drug potency, so it is important to develop new targets for tumor therapy. The expression of Type III transforming growth factor β receptor (TGFBR3) is upregulated in colon, breast, and prostate cancer cells, and plays an important role in the occurrence and development of these cancers, so TGFBR3 may be developed as a novel target for tumor therapy, but so far there is no report on this research. In this study, the structure of bone morphogenetic protein 4 (BMP4), one of the ligands of TGFBR3 was analyzed through the docking analysis with TGFBR3 and sequence charge characteristic analysis, and a functional tumor-targeting penetrating peptide T3BP was identified. The results of fluorescent labeling experiments showed that T3BP could target and efficiently enter tumor cells with high expression of TGFBR3, especially A549 cells. When the expression of TGFBR3 on the surface of tumor cells (HeLa) was knocked down by RNA interference, the high delivery efficiency of T3BP was correspondingly reduced by 40%, indicating that the delivery was TGFBR3-dependent. Trichosanthin (TCS, a plant-derived ribosome inactivating protein) fused with T3BP can enhance the inhibitory activity of the fusion protein on A549 cells by more than 200 times that of TCS alone. These results indicated that T3BP, as a novel targeting peptide that can efficiently bind TGFBR3 and be used for targeted therapy of tumors with high expression of TGFBR3. This study enriches the supply of tumor-targeting peptides and provides a new potential application option for the treatment of tumors with high expression of TGFBR3.

摘要

近年来,靶向治疗在癌症治疗中越来越受到关注。然而,由于肿瘤类型的多样性和肿瘤表面靶位的突变,一些现有的靶标不再适用于肿瘤治疗。此外,单一靶向药物的长期给药也会导致耐药性,从而降低药物的效力,因此开发新的肿瘤治疗靶标非常重要。III 型转化生长因子 β 受体(TGFBR3)在结肠、乳腺和前列腺癌细胞中的表达上调,并在这些癌症的发生和发展中发挥重要作用,因此 TGFBR3 可能被开发为肿瘤治疗的新靶标,但迄今为止,尚未有关于该研究的报道。在这项研究中,通过与 TGFBR3 的对接分析和序列电荷特性分析,分析了骨形态发生蛋白 4(BMP4)的结构,该结构是 TGFBR3 的配体之一,并鉴定了一种具有功能的肿瘤靶向穿透肽 T3BP。荧光标记实验结果表明,T3BP 可以靶向并有效地进入 TGFBR3 高表达的肿瘤细胞,尤其是 A549 细胞。当肿瘤细胞(HeLa)表面 TGFBR3 的表达被 RNA 干扰敲低时,T3BP 的高递药效率相应降低了 40%,表明递药是 TGFBR3 依赖性的。与 T3BP 融合的天花粉蛋白(TCS,一种植物来源的核糖体失活蛋白)可使融合蛋白对 A549 细胞的抑制活性提高 200 多倍,这表明 T3BP 是一种新型的靶向肽,可有效地与 TGFBR3 结合,用于治疗 TGFBR3 高表达的肿瘤。这项研究丰富了肿瘤靶向肽的供应,为治疗 TGFBR3 高表达的肿瘤提供了新的潜在应用选择。

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