详细信息
Improved breast cancer cell-specific intracellular drug delivery and therapeutic efficacy by coupling decoration with cell penetrating peptide and SP90 peptide ( SCI-EXPANDED收录)
文献类型:期刊文献
英文题名:Improved breast cancer cell-specific intracellular drug delivery and therapeutic efficacy by coupling decoration with cell penetrating peptide and SP90 peptide
作者:Fan, Li-Qiang[1];Du, Guo-Xiu[1];Li, Peng-Fei[1];Li, Ming-Wei[1];Sun, Yao[1];Zhao, Li-Ming[1]
机构:[1]East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
年份:2016
卷号:84
起止页码:1783
外文期刊名:BIOMEDICINE & PHARMACOTHERAPY
收录:;WOS:【SCI-EXPANDED(收录号:WOS:000390438100208)】;
基金:This work was partially supported by the National Natural Science Foundation of China (No.81071252).
语种:英文
外文关键词:Cell-penetrating peptide; Homing peptide; Targeted drug delivery; Breast cancer therapy; VPR
摘要:Lack of satisfactory specificity towards tumor cells and poor intracellular delivery efficacy are the major drawbacks with conventional cancer chemotherapy. Conjugated anticancer drugs to targeting moieties e.g. to peptides with the ability to recognize cancer cells and to cell penetrating peptide can improve these characteristics, respectively. Combining a tumor homing peptide with an appropriate cell-penetrating peptide can enhance the tumor-selective internalization efficacy of the carrying cargo molecules. In the present study, the breast cancer homing ability of SP90 peptide and the synergistic effect of SP90 with a cell-penetrating peptide(C peptide) were evaluated. SP90 and chimeric peptide SP90-C specifically targeted cargo molecule into breast cancer cells, especially triple negative MDA-MB-231 cell, in a dose-and time-dependent manner, but not normal breast cells and other cancer cells, while C peptide alone had no cell-selectivity. SP90-C increased the intracellular delivery efficiency by 12-fold or 10-fold compared to SP90 or C peptide alone, respectively. SP90 and SP90-C conjugation increased the anti-proliferative and apoptosis-inducing activity of HIV-1 Vpr, a potential novel anticancer protein drug, to breast cancer cell but not normal breast cell by arresting cells in G2/M phase. With excellent breast cancer cell-selective penetrating efficacy, SP90-C appears as a promising candidate vector for targeted anticancer drug delivery. SP90-VPR-C is a potential novel breast cancer-targeted anticancer agent for its high anti-tumor activity and low toxicity. (C) 2016 Elsevier Masson SAS. All rights reserved.
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