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双受体靶向细胞穿透肽修饰脂质体用于脑胶质瘤和乳腺癌术后复发治疗。

Dual Receptor Targeting Cell Penetrating Peptide Modified Liposome for Glioma and Breast Cancer Postoperative Recurrence Therapy.

机构信息

Key Laboratory of Drug Targeting and Drug Delivery Systems, Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu, Sichuan, People's Republic of China.

Ophthalmology Department, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China.

出版信息

Pharm Res. 2018 Apr 26;35(7):130. doi: 10.1007/s11095-018-2399-0.

Abstract

PURPOSE

Cell penetrating peptides (CPPs) were widely used as motifs for drug delivery to tumor. In former study, an RGD reverse sequence dGR was used to develop active-targeting liposome R8dGR-Lip, which showed well penetrating ability and treatment efficiency on glioma model. However, recurrence after tumor resection caused by post-operative residual cancer cells was a huge obstacle in tumor treatment. In consideration of the effective anti-cancer effect of PTX-R8dGR-Lip when treating glioma in former study, we decide to evaluate its pharmacodynamics on tumor resection models, which were more invasive and resistant.

METHOD

In vitro, the effectiveness of PTX-R8dGR-Lip in reducing tumor initiating cell (TIC) was investigated using mammosphere formation. In vivo, the inhibition efficiency of PTX-R8dGR-Lip on C6 glioma recurrence and 4 T1 breast cancer recurrence model were evaluated, including tumor bioluminescence imaging, survival rate and immumohistochemical staining, etc..

RESULTS

C6 mammosphere formation rate of PTX-R8dGR-Lip group was 48.06 ± 2.72%, and 4 T1 mammosphere formation rate of PTX-R8dGR-Lip group was 39.51 ± 4.02% when PBS group was set as 100%. C6 and 4 T1 bioluminescent tumor resected model were established, then effectiveness of different PTX-loaded preparations were evaluated on these two models. PTX-R8dGR-Lip could obviously inhibit tumor recurrence, prolong survival rate and reduce tumor tissue invasion.

CONCLUSION

PTX-R8dGR-Lip could reduce post-operative recurrence rate, prolong survival time, and decrease the proliferation of residual cancer cells through regulating the expression of recurrence-related cytokines.

摘要

目的

细胞穿透肽(CPPs)被广泛用作递药至肿瘤的基序。在之前的研究中,使用 RGD 反向序列 dGR 开发了主动靶向脂质体 R8dGR-Lip,该脂质体在神经胶质瘤模型中表现出良好的穿透能力和治疗效果。然而,肿瘤切除术后由于术后残留癌细胞引起的复发是肿瘤治疗的巨大障碍。考虑到 PTX-R8dGR-Lip 在治疗神经胶质瘤方面的有效抗癌作用,我们决定评估其在肿瘤切除模型中的药效学,这些模型更具侵袭性和耐药性。

方法

在体外,使用球体形成实验研究 PTX-R8dGR-Lip 减少肿瘤起始细胞(TIC)的效果。在体内,通过肿瘤生物发光成像、存活率和免疫组织化学染色等方法评估 PTX-R8dGR-Lip 对 C6 神经胶质瘤复发和 4T1 乳腺癌复发模型的抑制效率。

结果

PTX-R8dGR-Lip 组的 C6 球体形成率为 48.06±2.72%,PTX-R8dGR-Lip 组的 4T1 球体形成率为 49.51±4.02%,以 PBS 组为 100%。建立了 C6 和 4T1 生物发光肿瘤切除模型,然后评估了不同载药制剂对这两种模型的效果。PTX-R8dGR-Lip 明显抑制肿瘤复发,延长存活率,减少肿瘤组织侵袭。

结论

PTX-R8dGR-Lip 通过调节与复发相关的细胞因子的表达,降低术后复发率,延长生存时间,减少残留癌细胞的增殖。

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