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Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria

[Image: see text] Two new bracelet cyclotides from roots of Pombalia calceolaria with potential anticancer activity have been characterized in this work. The cyclotides Poca A and B (1 and 2) and the previously known CyO4 (3) were de novo sequenced by MALDI-TOF/TOF mass spectrometry (MS). The MS(2)...

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Autores principales: Pinto, Meri Emili F., Najas, Jhenny Z. G., Magalhães, Luma G., Bobey, Antonio F., Mendonça, Jacqueline N., Lopes, Norberto P., Leme, Flávia M., Teixeira, Simone P., Trovó, Marcelo, Andricopulo, Adriano D., Koehbach, Johannes, Gruber, Christian W., Cilli, Eduardo Maffud, Bolzani, Vanderlan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974699/
https://www.ncbi.nlm.nih.gov/pubmed/29757646
http://dx.doi.org/10.1021/acs.jnatprod.7b00969
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author Pinto, Meri Emili F.
Najas, Jhenny Z. G.
Magalhães, Luma G.
Bobey, Antonio F.
Mendonça, Jacqueline N.
Lopes, Norberto P.
Leme, Flávia M.
Teixeira, Simone P.
Trovó, Marcelo
Andricopulo, Adriano D.
Koehbach, Johannes
Gruber, Christian W.
Cilli, Eduardo Maffud
Bolzani, Vanderlan S.
author_facet Pinto, Meri Emili F.
Najas, Jhenny Z. G.
Magalhães, Luma G.
Bobey, Antonio F.
Mendonça, Jacqueline N.
Lopes, Norberto P.
Leme, Flávia M.
Teixeira, Simone P.
Trovó, Marcelo
Andricopulo, Adriano D.
Koehbach, Johannes
Gruber, Christian W.
Cilli, Eduardo Maffud
Bolzani, Vanderlan S.
author_sort Pinto, Meri Emili F.
collection PubMed
description [Image: see text] Two new bracelet cyclotides from roots of Pombalia calceolaria with potential anticancer activity have been characterized in this work. The cyclotides Poca A and B (1 and 2) and the previously known CyO4 (3) were de novo sequenced by MALDI-TOF/TOF mass spectrometry (MS). The MS(2) spectra were examined and the amino acid sequences were determined. The purified peptides were tested for their cytotoxicity and effects on cell migration of MDA-MB-231, a triple-negative breast cancer cell line. The isolated cyclotides reduced the number of cancer cells by more than 80% at 20 μM, and the concentration-related cytotoxic responses were observed with IC(50) values of 1.8, 2.7, and 9.8 μM for Poca A (1), Poca B (2), and CyO4 (3), respectively. Additionally, the inhibition of cell migration (wound-healing assay) exhibited that CyO4 (3) presents an interesting activity profile, in being able to inhibit cell migration (50%) at a subtoxic concentration (2 μM). The distribution of these cyclotides in the roots was analyzed by MALDI imaging, demonstrating that all three compounds are present in the phloem and cortical parenchyma regions.
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spelling pubmed-59746992018-05-31 Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria Pinto, Meri Emili F. Najas, Jhenny Z. G. Magalhães, Luma G. Bobey, Antonio F. Mendonça, Jacqueline N. Lopes, Norberto P. Leme, Flávia M. Teixeira, Simone P. Trovó, Marcelo Andricopulo, Adriano D. Koehbach, Johannes Gruber, Christian W. Cilli, Eduardo Maffud Bolzani, Vanderlan S. J Nat Prod [Image: see text] Two new bracelet cyclotides from roots of Pombalia calceolaria with potential anticancer activity have been characterized in this work. The cyclotides Poca A and B (1 and 2) and the previously known CyO4 (3) were de novo sequenced by MALDI-TOF/TOF mass spectrometry (MS). The MS(2) spectra were examined and the amino acid sequences were determined. The purified peptides were tested for their cytotoxicity and effects on cell migration of MDA-MB-231, a triple-negative breast cancer cell line. The isolated cyclotides reduced the number of cancer cells by more than 80% at 20 μM, and the concentration-related cytotoxic responses were observed with IC(50) values of 1.8, 2.7, and 9.8 μM for Poca A (1), Poca B (2), and CyO4 (3), respectively. Additionally, the inhibition of cell migration (wound-healing assay) exhibited that CyO4 (3) presents an interesting activity profile, in being able to inhibit cell migration (50%) at a subtoxic concentration (2 μM). The distribution of these cyclotides in the roots was analyzed by MALDI imaging, demonstrating that all three compounds are present in the phloem and cortical parenchyma regions. American Chemical Society and American Society of Pharmacognosy 2018-05-14 2018-05-25 /pmc/articles/PMC5974699/ /pubmed/29757646 http://dx.doi.org/10.1021/acs.jnatprod.7b00969 Text en Copyright © 2018 American Chemical Society and American Society of Pharmacognosy This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Pinto, Meri Emili F.
Najas, Jhenny Z. G.
Magalhães, Luma G.
Bobey, Antonio F.
Mendonça, Jacqueline N.
Lopes, Norberto P.
Leme, Flávia M.
Teixeira, Simone P.
Trovó, Marcelo
Andricopulo, Adriano D.
Koehbach, Johannes
Gruber, Christian W.
Cilli, Eduardo Maffud
Bolzani, Vanderlan S.
Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria
title Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria
title_full Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria
title_fullStr Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria
title_full_unstemmed Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria
title_short Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria
title_sort inhibition of breast cancer cell migration by cyclotides isolated from pombalia calceolaria
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974699/
https://www.ncbi.nlm.nih.gov/pubmed/29757646
http://dx.doi.org/10.1021/acs.jnatprod.7b00969
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