Self-Triggered Apoptosis Enzyme Prodrug Therapy (STAEPT): Enhancing Targeted Therapies via Recurrent Bystander Killing Effect by Exploiting Caspase-Cleavable Linker
- Authors
- Chung, Seung Woo; Choi, Jeong Uk; Cho, Young Seok; Kim, Ha Rin; Won, Tae Hyung; Dimitrion, Peter; Jeon, Ok-Cheol; Kim, Seong Who; Kim, In-San; Kim, Sang Yoon; Byun, 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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