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This work is licensed under a Creative Commons Attribution 4.0 International License.
In vitro Cytotoxic Activity against MCF-7 Breast Cancer Cells Line: Pregabalin and Chiral Amino Acid-based Peptides
Corresponding Author(s) : H.M. Parekh
Asian Journal of Chemistry,
Vol. 34 No. 4 (2022): Vol 34 Issue 4, 2022
Abstract
Because of the medicinal application of peptides in the current drug discovery process, we report the synthesis and in vitro anticancer activity of various pregabalin containing peptides using chiral amino acids. The structures of newly synthesized compounds were assigned based on IR, 1H NMR, 13C NMR and mass spectral analysis. Synthesized peptides were screened for their anticancer activity on human breast cancer MCF-7 cells line by MMT assays method. Evaluation of anticancer activity shown that compound 13a (16.65% cell proliferation) was found to be most active against selected MCF-7 cell line.
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References
K. Kapadiya and R. Khunt, Lett. Drug Des. Discov., 16, 21 (2018); https://doi.org/10.2174/1570180815666180419151742
S. Wanandi, A. Limanto, E. Yunita, R. Syahrani, M. Louisa, A.E. Wibowo and S. Arumsari, PLoS One, 16, e0247694 (2021); https://doi.org/10.1371/journal.pone.0247694
D. Chowrasia, C. Karthikeyan, L. Choure, Sahabjada, M. Gupta, M. Arshad and P. Trivedi, Arab. J. Chem., 10, 2424 (2017); https://doi.org/10.1016/j.arabjc.2013.08.026
M. Falzon and P. Du, Endocrinology, 141, 1882 (2000); https://doi.org/10.1210/endo.141.5.7470
K. Miller, L. Nogueira, A. Mariotto, J. Rowland, K. Yabroff, C. Alfano, A. Jemal, J. Kramer and R. Siegel, Cancer J. Clin., 69, 363 (2019); https://doi.org/10.3322/caac.21565
S. Marsh and H.L. McLeod, Expert Opin. Pharmacother., 8, 119 (2007); https://doi.org/10.1517/14656566.8.2.119
N. Razak, N. Abu, W. Ho, N.R. Zamberi, S.W. Tan, N.B. Alitheen, K. Long and S.K. Yeap, Sci. Rep., 9, 1514 (2019); https://doi.org/10.1038/s41598-018-37796-w
S. Atreya, Indian J. Palliat. Care, 22, 101 (2016); https://doi.org/10.4103/0973-1075.173941
S. Wolf, D. Barton, L. Kottschade, A. Grothey and C. Loprinzi, J. Eur, Cancer, 44, 1507 (2008); https://doi.org/10.1016/j.ejca.2008.04.018
K. Sjolund, Y. Yang, K. Lee and M. Resnick, Pain Ther., 2, 37 (2013); https://doi.org/10.1007/s40122-013-0009-8
S.Y. Yoon and J. Oh, Korean J. Intern. Med., 33, 1058 (2018); https://doi.org/10.3904/kjim.2018.162
A. Cicero, F. Fogacci and A. Colletti, Br. J. Pharmacol., 174, 1378 (2017); https://doi.org/10.1111/bph.13608
Y. Mine, H. Munir, Y. Nakanishi and D. Sugiyama, Anticancer Res., 36, 3565 (2016).
L. Yang, H. Liu, M. Long, X. Wang, F. Lin, Z. Gao and H. Zhang, OncoTargets Ther., 11, 2409 (2018); https://doi.org/10.2147/OTT.S154337
L. Depau, J. Brunetti, C. Falciani, S. Scali, G. Riolo, E. Mandarini, A. Pini and L. Bracci, Oncotarget, 8, 76141 (2017); https://doi.org/10.18632/oncotarget.19056
M. Xie, D. Liu and Y. Yang, Open Biol., 10, 200004 (2020); https://doi.org/10.1098/rsob.200004
Y. Liscano, J. Onate-Garzon and J. Delgado, Molecules, 25, 4245 (2020); https://doi.org/10.3390/molecules25184245
L. Wang, C. Dong, X. Li, W. Han and X. Su, Oncol. Rep., 38, 637 (2017); https://doi.org/10.3892/or.2017.5778
F.U. Vaidya, R. Sharma, S. Shaikh, D. Ray, V.K. Aswal and C. Pathak, Cancer Reports, 2, e1133 (2019); https://doi.org/10.1002/cnr2.1133
S. Bondock, S. Alqahtani and A. Fouda, J. Heterocycl. Chem., 58, 56 (2021); https://doi.org/10.1002/jhet.4148
M. Wieduwilt and M. Moasser, Cell. Mol. Life Sci., 65, 1566 (2008); https://doi.org/10.1007/s00018-008-7440-8
M. Ghorab, M. Alsaid, M. El-Gaby, M. Elaasser and Y. Nissan, Chem. Cent. J., 11, 32 (2017); https://doi.org/10.1186/s13065-017-0258-4
C. Pang, C. Sun, J. Wang, D. Xiao, L. Ding and H. Bu, Sci. China Chem., 56, 702 (2013); https://doi.org/10.1007/s11426-013-4840-x
C. Martinez-Perez, C. Ward, A. Turnbull, P. Mullen, G. Cook, J. Meehan, E.J. Jarman, P.I.T. Thomson, C.J. Campbell, D. McPhail, D.J. Harrison and S.P. Langdon, Br. J. Cancer, 114, 905 (2016); https://doi.org/10.1038/bjc.2016.6
R.R.J. Arroo, V. Androutsopoulos, K. Beresford, K. Ruparelia, S. Surichan, N. Wilsher and G.A. Potter, Phytochem. Rev., 8, 375 (2009); https://doi.org/10.1007/s11101-009-9128-6
M. Egorin, Cancer Chemother. Pharmacol., 42(S1), S22 (1998); https://doi.org/10.1007/s002800051076