Self-Triggered Apoptosis Enzyme Prodrug Therapy (STAEPT): Enhancing Targeted Therapies via Recurrent Bystander Killing Effect by Exploiting Caspase-Cleavable Linker

Authors
Chung, Seung WooChoi, Jeong UkCho, Young SeokKim, Ha RinWon, Tae HyungDimitrion, PeterJeon, Ok-CheolKim, Seong WhoKim, In-SanKim, Sang YoonByun, Youngro
Issue Date
2018-07
Publisher
WILEY
Citation
ADVANCED SCIENCE, v.5, no.7
Abstract
Tumor heterogeneity is associated with the therapeutic failures of targeted therapies. To overcome such heterogeneity, a novel targeted therapy is proposed that could kill tumor populations with diverse phenotypes by delivering nonselective cytotoxins to target-positive cells as well as to the surrounding tumor cells via a recurrent bystander killing effect. A representative prodrug is prepared that targets integrin alpha v beta 3 and releases cytotoxins upon entering cells or by caspase-3. This allows the prodrug to kill integrin alpha v beta 3-positive cells and upregulate caspase-3, which in turn, activates the prodrug to release a cytotoxin that could subsequently diffuse into and kill the neighboring tumor cells. Apoptotic cells further upregulate and release caspase-3, which activate more prodrugs leading to another round of adjacent cell death and caspase-3 release. Thus, the bystander killing effect could occur repeatedly, leading to augmented and widespread anticancer activity. This strategy provides an avenue that could advance the current targeted therapy.
Keywords
TUMOR HETEROGENEITY; DRUG-DELIVERY; IN-VIVO; DOXORUBICIN; THERAPEUTICS; EVOLUTION; ESTERASE; RGD; TUMOR HETEROGENEITY; DRUG-DELIVERY; IN-VIVO; DOXORUBICIN; THERAPEUTICS; EVOLUTION; ESTERASE; RGD; bystander killing effects; cancer therapies; caspases; prodrugs; target therapies
ISSN
2198-3844
URI
https://pubs.kist.re.kr/handle/201004/121191
DOI
10.1002/advs.201800368
Appears in Collections:
KIST Article > 2018
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