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Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria
Author(s) -
Meri Emili F. Pinto,
Jhenny Z. G. Najas,
Luma G. Magalhães,
Antonio F. Bobey,
Jacqueline Nakau Mendonça,
Norberto Peporine Lopes,
Flávia Maria Leme,
Simone Pádua Teixeira,
Marcelo Trovó,
Adriano D. Andricopulo,
Johannes Koehbach,
Christian W. Gruber,
Eduardo Maffud Cilli,
Vanderlan da Silva Bolzani
Publication year - 2018
Publication title -
journal of natural products
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 139
eISSN - 1520-6025
pISSN - 0163-3864
DOI - 10.1021/acs.jnatprod.7b00969
Subject(s) - cytotoxicity , cell culture , chemistry , cell migration , cancer cell , biochemistry , biology , cell , cancer , in vitro , genetics
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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