Cytotoxicity of cashew flavonoids towards malignant cell lines

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Citações na Scopus
41
Tipo de produção
article
Data de publicação
2012
Título da Revista
ISSN da Revista
Título do Volume
Editora
ELSEVIER GMBH, URBAN & FISCHER VERLAG
Autores
KONAN, Nzi Andre
LINCOPAN, Nilton
DIAZ, Ingrit Elida Collantes
TIBA, Mirtes Midori Tanae
MENDES, Joao Gustavo Pessini Amarante
BACCHI, Elfriede Marianne
SPIRA, Beny
Citação
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, v.64, n.5, p.435-440, 2012
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
The leaves of the Cashew plant (Anacardium occidentale L.) are used by the folk medicine in South America and West Africa. This plant is rich in flavonoids, which are polyphenolic compounds widespread in plants, and that have diverse physiological effects. In a sub-acute toxicity assay it was found that an ethanolic extract of Cashew leaves elicited lymphopenia in rats. The extract was also found to be cytotoxic and to induce apoptosis in Jurkat (acute lymphoblastic leukemia) cells. The crude ethanolic extract was fractionated and resolved by HPLC. One of the four fractions obtained led to the isolation of the biflavonoid agasthisflavone. [H-3]-thymidine incorporation assays and flow cytometry analysis showed that the isolated compound displayed a high anti-proliferative effect in Jurkat cells with an IC50 of 2.4 mu g/ml (4.45 mu M). The effect of agathisflavone on the acute promyelocytic leukemia cell line HL60, Burkitt lymphoma Raji cells and Hep-2 laryngeal carcinoma cells was also tested. The two latter ones were only mildly affected by agathisflavone. It is also shown that agathisflavone induces apoptosis in Jurkat cells and it this proposed that this is the likely mechanism of agathisflavone specific cytotoxicity.
Palavras-chave
Cashew, Rats, Leukemia cells
Referências
  1. Asirvatham AL, 2004, J IMMUNOL, V173, P4806
  2. Chaabi M, 2007, PLANTA MED, V73, P1284, DOI 10.1055/s-2007-990218
  3. COLLINS SJ, 1977, NATURE, V270, P347, DOI 10.1038/270347a0
  4. Cushnie TPT, 2005, INT J ANTIMICROB AG, V26, P343, DOI 10.1016/j.ijantimicag.2005.09.002
  5. de Carvalho M, 2007, INDIAN J PHARM, V39, P184
  6. Grynberg NF, 2002, BRAZ J MED BIOL RES, V35, P819, DOI 10.1590/S0100-879X2002000700009
  7. Harborne J B, 1986, Prog Clin Biol Res, V213, P15
  8. Kaatsch P, 2010, CANCER TREAT REV, V36, P277, DOI 10.1016/j.ctrv.2010.02.003
  9. Kim HP, 2008, ARCH PHARM RES, V31, P265, DOI [10.1007/s12272-001-1151-3, 10.1007/s00000-001-1151-3]
  10. Kirszberg C, 2003, PHYTOTHER RES, V17, P1054, DOI 10.1002/ptr.1297
  11. Konan NA, 2007, J ETHNOPHARMACOL, V110, P30, DOI 10.1016/j.jep.2006.08.033
  12. Lerner A, 2006, BIOCHEM J, V393, P21, DOI 10.1042/BJ20051368
  13. Lincopan N, 2006, EXP TOXICOL PATHOL, V58, P175, DOI 10.1016/j.etp.2006.07.002
  14. Lucas DM, 2009, BLOOD, V113, P4656, DOI 10.1182/blood-2008-09-175430
  15. Mkounga P, 2009, NAT PROD COMMUN, V4, P803
  16. MOORE AE, 1955, CANCER RES, V15, P598
  17. Newman DJ, 2007, J NAT PROD, V70, P461, DOI 10.1021/np068054v
  18. NICOLETTI I, 1991, J IMMUNOL METHODS, V139, P271, DOI 10.1016/0022-1759(91)90198-O
  19. Pang XF, 2009, CANCER RES, V69, P518, DOI 10.1158/0008-5472.CAN-08-2531
  20. Park KH, 2006, BIOORG MED CHEM LETT, V16, P5580, DOI 10.1016/j.bmcl.2006.08.032
  21. Perez-Tomas R, 2003, HISTOL HISTOPATHOL, V18, P379
  22. PULVERTAFT J V, 1964, Lancet, V1, P238
  23. Souza-Fagundes EM, 2003, EXP CELL RES, V290, P420, DOI 10.1016/S0014-4827(03)00350-1
  24. Svenningsen AB, 2006, J ETHNOPHARMACOL, V103, P276, DOI 10.1016/j.jep.2005.08.012
  25. WEISS A, 1984, J IMMUNOL, V133, P123
  26. Zhang LZ, 2008, P NATL ACAD SCI USA, V105, P19532, DOI 10.1073/pnas.0806152105
  27. Zhu WH, 1998, LIFE SCI, V63, P265, DOI 10.1016/S0024-3205(98)00270-7