Tools
Tools
Shaheen, Farzana, Nadeem-ul-Haque, Muhammad, Ahmed, Aqeel, Simjee, Shabana U., Ganesan, A. 
ORCID: https://orcid.org/0000-0003-4862-7999, Jabeen, Almas, Shah, Zafar Ali and Choudhary, M. Iqbal
(2018)
Synthesis of breast cancer targeting conjugate of temporin-SHa analog and its effect on pro- and anti-apoptotic protein expression in MCF-7 cells.
Peptides, 106.
pp. 68-82.
ISSN 0196-9781
Preview |
PDF (Accepted manuscript)
- Accepted Version
Available under License Creative Commons Attribution Non-commercial No Derivatives. Download (1MB) | Preview |
Abstract
The frog natural product temporin-SHa (FLSGIVGMLGKLFamide) is a potent antimicrobial peptide, as is the analog [S3K]SHa. By solid-phase synthesis, we prepared temporin-SHa and several temporin-SHa analogs with one or more D-alanine residues incorporated. The natural product and the analog [G10a]SHa were found to be cytotoxic in mammalian cell lines and induce cell death. To achieve selectivity, we conjugated the analog [G10a]SHa with a breast cancer targeting peptide (BCTP). The resulting peptide temporin [G10a]SHa-BCTP conjugate was selectively active against the MCF-7 breast cancer cell line with no cytotoxicity in NIH-3T3 fibroblasts. Unlike the natural product or [G10a]SHa, the conjugated peptide induced apoptosis, down regulating the expression of Bcl-2 and survivin and up regulating Bax and caspase-3.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | antimicrobial peptides,temporin-sha analogs,breast cancer targeting peptide conjugate,apoptosis,bcl-2,survivin,caspase-3,sdg 3 - good health and well-being ,/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being |
| Faculty \ School: | Faculty of Science > School of Pharmacy |
| UEA Research Groups: | Faculty of Science > Research Groups > Chemical Biology and Medicinal Chemistry (former - to 2021) |
| Related URLs: | |
| Depositing User: | LivePure Connector |
| Date Deposited: | 13 Jul 2018 09:31 |
| Last Modified: | 22 Oct 2022 03:57 |
| URI: | https://ueaeprints.uea.ac.uk/id/eprint/67613 |
| DOI: | 10.1016/j.peptides.2018.07.002 |
Downloads
Downloads per month over past year
Actions (login required)
 |
View Item |