Loading of ”cocktail siRNAs” into extracellular vesicles via TAT-DRBD peptide for the treatment of castration-resistant prostate cancer-Reference-Cited by-同舟云学术

Loading of ”cocktail siRNAs” into extracellular vesicles via TAT-DRBD peptide for the treatment of castration-resistant prostate cancer

Published:2022-02-16 Issue:1 Volume:23 Page:163-172
ISSN:1538-4047
Container-title:Cancer Biology & Therapy
language:en
Short-container-title:Cancer Biology & Therapy

Author:

Diao Yanjun¹^ORCID,Wang Gangqiang¹,Zhu Bingbing¹,Li Zhuo²,Wang Shan³,Yu Lijuan¹,Li Rui¹,Fan Weixiao¹,Zhang Yue¹,Zhou Lei¹^ORCID,Yang Liu¹,Hao Xiaoke¹,Liu Jiayun¹

Affiliation:

1. Department of Clinical Laboratory Medicine, Xijing Hospital, Fourth Military Medical University, Xi’an, Shaanxi, China

2. Department of Laboratory Medicine, The First Affiliated Hospital of Xi’an Medical University, Xi’an, Shaanxi, China

3. Department of Clinical Laboratory Medicine, The Fourth Hospital of Xi’an, Xi’an, Shaanxi, China

Funder

National Natural Science Foundation of China

Publisher

Informa UK Limited

Subject

Cancer Research,Pharmacology,Oncology,Molecular Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/15384047.2021.2024040

Reference27 articles.

1. Exosomes as nanocarriers for siRNA delivery: paradigms and challenges

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4. Leveraging therapeutic potential of multi-targeted siRNA inhibitors

5. Androgen-independent LNCaP cells are a subline of LNCaP cells with a more aggressive phenotype and androgen suppresses their growth by inducing cell cycle arrest at the G1 phase

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