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本文引用的文献

1
FKBPL: a marker of good prognosis in breast cancer.FKBPL:乳腺癌良好预后的一个标志物。
Oncotarget. 2015 May 20;6(14):12209-23. doi: 10.18632/oncotarget.3528.
2
FKBPL is a critical antiangiogenic regulator of developmental and pathological angiogenesis.FKBPL是发育性和病理性血管生成的关键抗血管生成调节因子。
Arterioscler Thromb Vasc Biol. 2015 Apr;35(4):845-54. doi: 10.1161/ATVBAHA.114.304539. Epub 2015 Mar 12.
3
Development and characterization of self-assembling nanoparticles using a bio-inspired amphipathic peptide for gene delivery.利用一种受生物启发的两亲性肽开发和表征用于基因传递的自组装纳米颗粒。
J Control Release. 2014 Sep 10;189:141-9. doi: 10.1016/j.jconrel.2014.06.048. Epub 2014 Jul 1.
4
Design, preparation and application of nucleic acid delivery carriers.核酸递送载体的设计、制备与应用。
Biotechnol Adv. 2014 Jul-Aug;32(4):804-17. doi: 10.1016/j.biotechadv.2013.11.004. Epub 2013 Nov 14.
5
Biological functionalization of drug delivery carriers to bypass size restrictions of receptor-mediated endocytosis independently from receptor targeting.药物递送载体的生物功能化,以独立于受体靶向绕过受体介导的内吞作用的尺寸限制。
ACS Nano. 2013 Dec 23;7(12):10597-611. doi: 10.1021/nn404719c. Epub 2013 Nov 20.
6
Targeting treatment-resistant breast cancer stem cells with FKBPL and its peptide derivative, AD-01, via the CD44 pathway.通过 CD44 通路,使用 FKBPL 及其肽衍生物 AD-01 靶向治疗抵抗型乳腺癌干细胞。
Clin Cancer Res. 2013 Jul 15;19(14):3881-93. doi: 10.1158/1078-0432.CCR-13-0595. Epub 2013 Jun 5.
7
A recombinant biopolymeric platform for reliable evaluation of the activity of pH-responsive amphiphile fusogenic peptides.用于可靠评估 pH 响应两亲融合肽活性的重组生物聚合平台。
Biomacromolecules. 2013 Jun 10;14(6):2033-40. doi: 10.1021/bm400380s. Epub 2013 May 30.
8
Systematic engineering of uniform, highly efficient, targeted and shielded viral-mimetic nanoparticles.系统工程化的均一、高效、靶向且屏蔽的病毒模拟纳米颗粒。
Small. 2013 Aug 26;9(16):2774-83. doi: 10.1002/smll.201300077. Epub 2013 Mar 7.
9
The anti-migratory effects of FKBPL and its peptide derivative, AD-01: regulation of CD44 and the cytoskeletal pathway.FKBPL 及其肽衍生物 AD-01 的抗迁移作用:对 CD44 和细胞骨架途径的调节。
PLoS One. 2013;8(2):e55075. doi: 10.1371/journal.pone.0055075. Epub 2013 Feb 15.
10
Cell-penetrating peptides (CPPs) as a vector for the delivery of siRNAs into cells.细胞穿透肽(CPPs)作为将小干扰RNA(siRNAs)递送至细胞的载体。
Mol Biosyst. 2013 May;9(5):855-61. doi: 10.1039/c2mb25467k.

RALA介导的FKBPL核酸治疗药物递送。

RALA-mediated delivery of FKBPL nucleic acid therapeutics.

作者信息

Bennett Rachel, Yakkundi Anita, McKeen Hayley D, McClements Lana, McKeogh Thomas J, McCrudden Cian M, Arthur Kenneth, Robson Tracy, McCarthy Helen O

机构信息

School of Pharmacy, Queen's University Belfast, 97 Lisburn Road, Belfast, BT9 7BL, Northern Ireland, UK.

Northern Ireland Molecular Pathology Laboratory, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.

出版信息

Nanomedicine (Lond). 2015 Oct;10(19):2989-3001. doi: 10.2217/nnm.15.115. Epub 2015 Sep 30.

DOI:10.2217/nnm.15.115
PMID:26419658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4910961/
Abstract

AIMS

RALA is a novel 30 mer bioinspired amphipathic peptide that is showing promise for gene delivery. Here, we used RALA to deliver the FK506-binding protein like - FKBPL gene (pFKBPL) - a novel member of the immunophilin protein family. FKBPL is a secreted protein, with overexpression shown to inhibit angiogenesis, tumor growth and stemness, through a variety of intra- and extracellular signaling mechanisms. We also elucidated proangiogenic activity and stemness after utilizing RALA to deliver siRNA (siFKBPL).

MATERIALS & METHODS: The RALA/pFKBPL and RALA/siFKBPL nanoparticles were characterized in terms of size, charge, stability and toxicity. Overexpression and knockdown of FKBPL was assessed in vitro and in vivo.

RESULTS

RALA delivered both pFKBPL and siFKBPL with less cytotoxicity than commercially available counterparts. In vivo, RALA/pFKBPL delivery retarded tumor growth, and prolonged survival with an associated decrease in angiogenesis, while RALA/siFKBPL had no effect on tumor growth rate or survival, but resulted in an increase in angiogenesis and stemness.

CONCLUSION

RALA is an effective delivery system for both FKBPL DNA and RNAi and highlights an alternative therapeutic approach to harnessing FKBPL's antiangiogenic and antistemness activity.

摘要

目的

RALA是一种新型的30聚体生物启发型两亲性肽,在基因递送方面显示出前景。在此,我们使用RALA递送FK506结合蛋白样-FKBPL基因(pFKBPL)——亲免素蛋白家族的一个新成员。FKBPL是一种分泌蛋白,过表达显示可通过多种细胞内和细胞外信号传导机制抑制血管生成、肿瘤生长和干性。我们还在利用RALA递送小干扰RNA(siFKBPL)后阐明了促血管生成活性和干性。

材料与方法

对RALA/pFKBPL和RALA/siFKBPL纳米颗粒的大小、电荷、稳定性和毒性进行了表征。在体外和体内评估了FKBPL的过表达和敲低情况。

结果

与市售同类产品相比,RALA递送pFKBPL和siFKBPL时细胞毒性更小。在体内,RALA/pFKBPL递送可延缓肿瘤生长,延长生存期,并伴有血管生成减少,而RALA/siFKBPL对肿瘤生长速率或生存期无影响,但导致血管生成和干性增加。

结论

RALA是一种用于FKBPL DNA和RNA干扰的有效递送系统,并突出了一种利用FKBPL的抗血管生成和抗干性活性的替代治疗方法。