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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.

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。

相似文献

1
RALA-mediated delivery of FKBPL nucleic acid therapeutics.RALA介导的FKBPL核酸治疗药物递送。
Nanomedicine (Lond). 2015 Oct;10(19):2989-3001. doi: 10.2217/nnm.15.115. Epub 2015 Sep 30.
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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.

引用本文的文献

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.
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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.

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