Cryptophycins: cytotoxic cyclodepsipeptides with potential for tumor targeting

Weiss C, Figueras Agustí E, Borbély AN, Sewald N (2017)
Journal of Peptide Science 23(7-8): 514-531.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Abstract / Bemerkung
Cryptophycins are a class of 16-membered highly cytotoxic macrocyclic depsipeptides isolated from cyanobacteria. The biological activity is based on their ability to interact with tubulin. They interfere with microtubule dynamics and prevent microtubules from forming correct mitotic spindles, which causes cell-cycle arrest and apoptosis. Their strong antiproliferative activities with 100-fold to 1000-fold potency compared with those of paclitaxel and vinblastine have been observed. Cryptophycins are highly promising drug candidates, as their biological activity is not negatively affected by P-glycoprotein, a drug efflux system commonly found in multidrug-resistant cancer cell lines and solid tumors. Cryptophycin-52 had been investigated in phase II clinical trials but failed because of its high neurotoxicity. Recently, cryptophycin conjugates with peptides and antibodies have been developed for targeted delivery in tumor therapy. Copyright © 2017 European Peptide Society and John Wiley & Sons, Ltd.
Stichworte
natural product; depsipeptide; total synthesis; biological activity; SAR; antimitotic agent; drug conjugate; bioconjugation; warhead
Erscheinungsjahr
2017
Zeitschriftentitel
Journal of Peptide Science
Band
23
Ausgabe
7-8
Seite(n)
514-531
Konferenz
Conference on Rokko Mountain
Konferenzort
Kobe, JAPAN
ISSN
1075-2617
eISSN
1099-1387
Page URI
https://pub.uni-bielefeld.de/record/2916981

Zitieren

Weiss C, Figueras Agustí E, Borbély AN, Sewald N. Cryptophycins: cytotoxic cyclodepsipeptides with potential for tumor targeting. Journal of Peptide Science. 2017;23(7-8):514-531.
Weiss, C., Figueras Agustí, E., Borbély, A. N., & Sewald, N. (2017). Cryptophycins: cytotoxic cyclodepsipeptides with potential for tumor targeting. Journal of Peptide Science, 23(7-8), 514-531. https://doi.org/10.1002/psc.3015
Weiss, Christine, Figueras Agustí, Eduard, Borbély, Adina Noémi, and Sewald, Norbert. 2017. “Cryptophycins: cytotoxic cyclodepsipeptides with potential for tumor targeting”. Journal of Peptide Science 23 (7-8): 514-531.
Weiss, C., Figueras Agustí, E., Borbély, A. N., and Sewald, N. (2017). Cryptophycins: cytotoxic cyclodepsipeptides with potential for tumor targeting. Journal of Peptide Science 23, 514-531.
Weiss, C., et al., 2017. Cryptophycins: cytotoxic cyclodepsipeptides with potential for tumor targeting. Journal of Peptide Science, 23(7-8), p 514-531.
C. Weiss, et al., “Cryptophycins: cytotoxic cyclodepsipeptides with potential for tumor targeting”, Journal of Peptide Science, vol. 23, 2017, pp. 514-531.
Weiss, C., Figueras Agustí, E., Borbély, A.N., Sewald, N.: Cryptophycins: cytotoxic cyclodepsipeptides with potential for tumor targeting. Journal of Peptide Science. 23, 514-531 (2017).
Weiss, Christine, Figueras Agustí, Eduard, Borbély, Adina Noémi, and Sewald, Norbert. “Cryptophycins: cytotoxic cyclodepsipeptides with potential for tumor targeting”. Journal of Peptide Science 23.7-8 (2017): 514-531.
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8 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Synthesis and Biological Evaluation of RGD⁻Cryptophycin Conjugates for Targeted Drug Delivery.
Borbély A, Figueras E, Martins A, Esposito S, Auciello G, Monteagudo E, Di Marco A, Summa V, Cordella P, Perego R, Kemker I, Frese M, Gallinari P, Steinkühler C, Sewald N., Pharmaceutics 11(4), 2019
PMID: 30939768
Octreotide Conjugates for Tumor Targeting and Imaging.
Figueras E, Martins A, Borbély A, Le Joncour V, Cordella P, Perego R, Modena D, Pagani P, Esposito S, Auciello G, Frese M, Gallinari P, Laakkonen P, Steinkühler C, Sewald N., Pharmaceutics 11(5), 2019
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Conjugates of Cryptophycin and RGD or isoDGR Peptidomimetics for Targeted Drug Delivery.
Borbély A, Figueras E, Martins A, Bodero L, Raposo Moreira Dias A, López Rivas P, Pina A, Arosio D, Gallinari P, Frese M, Steinkühler C, Gennari C, Piarulli U, Sewald N., ChemistryOpen 8(6), 2019
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