The effects of the mycotoxin austdiol on cell cycle progression, cytotoxicity and genotoxicity in Chinese hamster ovary (CHO-K1) cells

被引:1
|
作者
Franchi, L. P. [1 ]
De Souza, T. A. J. [1 ]
Andrioli, W. J. [2 ,3 ]
Lima, I. M. S. [1 ]
Bastos, J. K. [2 ]
Takahashi, C. S. [1 ,3 ]
机构
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Genet, Bloco G Ave Bandeirantes 3900, BR-14049900 Monte Alegre do Sul, SP, Brazil
[2] Univ Sao Paulo, Sch Pharmaceut Sci Ribeirao Preto, Ave Cafe S-N, BR-14040903 Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Fac Philosophy Sci & Letters Ribeirao Preto, Ave Bandeirantes 3900, BR-14040900 Vila Monte Alegre, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
clonogenic assay; comet assay; cytome/micronucleus test; flow cytometry; metabolite; TOPOISOMERASE-II INHIBITORS; DNA-INTERCALATING AGENTS; POLYCYCLIC AROMATIC-HYDROCARBONS; MICRONUCLEUS CYTOME ASSAY; IN-VITRO; DROSOPHILA-MELANOGASTER; MOLECULAR-MECHANISMS; MAMMALIAN-CELLS; SOMATIC-CELLS; OCHRATOXIN;
D O I
10.3920/WMJ2015.1907
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Austdiol is a mycotoxin mainly produced by Aspergillus ustus and Mycoleptodiscus indicus. These fungi are found in rye, oats, barley, corn and feed grains; thus, as a potential contaminant of human food and animal feed, this mycotoxin is of great concern. As such, the elucidation of the cytotoxicity and mutagenicity of austdiol is important. In this study, austdiol was purified from a rice-oat solid medium culture of M. indicus using chromatographic separation techniques. Chinese hamster ovary (CHO-K1) cells were then used to study the effect of austdiol on mammalian cell cycle, clonogenicity and DNA damage. Austdiol induced cell cycle arrest in G2/M phase, with a decreased S phase population and increased sub-G1 population. Austdiol also increased the polyploid population. These events resulted in cell death detected 7 days after treatment by clonogenic assay. DNA damage represents the main mechanism of action of austdiol, which induces DNA breaks and increases the frequency of micronuclei and nucleoplasmic bridges in binucleated cells in a CHO-K1 cell line. Moreover, cells exposed to austdiol and doxorubicin (DXR) combined treatments presented a reduced number of colonies and increased frequencies of micronuclei and nucleoplasmic bridges compared with negative control and cells treated with austdiol or DXR alone.
引用
收藏
页码:237 / 246
页数:10
相关论文
共 50 条
  • [21] THE INSULIN-RECEPTOR AS A TRANSMITTER OF A MITOGENIC SIGNAL IN CHINESE-HAMSTER OVARY CHO-K1 CELLS
    MAMOUNAS, M
    GERVIN, D
    ENGLESBERG, E
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (23) : 9294 - 9298
  • [22] New mutations and phenotypes associated with glutamate and aspartate transport in Chinese hamster ovary (CHO-K1) cells
    Igo, RP
    Ash, JF
    SOMATIC CELL AND MOLECULAR GENETICS, 1996, 22 (02) : 87 - 103
  • [23] Protective Effects of Rosmarinic Acid and Epigallocatechin Gallate Against DoxorubicinInduced Cytotoxicity and Genotoxicity in CHO-K1 Cells
    Helvacioglu, Sinem
    Hamitoglu, Muhammed
    Yildirim, Ecem
    Vural Korkut, Senay
    Yaba, Aylin
    Aydin, Ahmet
    TURKISH JOURNAL OF PHARMACEUTICAL SCIENCES, 2024, 21 (06) : 536 - 543
  • [24] CELL CYCLE-RELATED VARIATIONS IN UV DAMAGE AND REPAIR CAPACITY IN CHINESE-HAMSTER (CHO-K1) CELLS
    COLLINS, ARS
    DOWNES, CS
    JOHNSON, RT
    JOURNAL OF CELLULAR PHYSIOLOGY, 1980, 103 (02) : 179 - 191
  • [25] Effect of Brazilian propolis (AF-08) on genotoxicity, cytotoxicity and clonogenic death of Chinese hamster ovary (CHO-K1) cells irradiated with 60Co gamma-radiation
    Santos, Geyza Spigoti
    Tsutsumi, Shigetoshi
    Vieira, Daniel Perez
    Bartolini, Paolo
    Okazaki, Kayo
    MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2014, 762 : 17 - 23
  • [26] Comparative study of the cytotoxic and genotoxic effects of titanium oxide and aluminium oxide nanoparticles in Chinese hamster ovary (CHO-K1) cells
    Di Virgilio, A. L.
    Reigosa, M.
    Arnal, P. M.
    Fernandez Lorenzo de Mele, M.
    JOURNAL OF HAZARDOUS MATERIALS, 2010, 177 (1-3) : 711 - 718
  • [27] Characterization of p53 in Chinese hamster cell lines CHO-K1, CHO-WBL, and CHL: implications for genotoxicity testing
    Hu, T
    Miller, CM
    Ridder, GM
    Aardema, MJ
    MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1999, 426 (01) : 51 - 62
  • [28] Sister chromatid exchanges and chromosomal aberrations in Chinese hamster ovary (CHO-K1) cells treated with the insecticide pirimicarb
    Soloneski, Sonia
    Larramendy, Marcelo L.
    JOURNAL OF HAZARDOUS MATERIALS, 2010, 174 (1-3) : 410 - 415
  • [29] Cytotoxicity and genotoxicity of stilbene derivatives in CHO-K1 and HepG2 cell lines
    Mizuno, Cassia Suemi
    Ampomaah, Winnifred
    Mendonca, Fernanda Ribeiro
    Andrade, Gabriela Carvalho
    Nazare da Silva, Ariel Maria
    Goulart, Mirian Oliveira
    dos Santos, Raquel Alves
    GENETICS AND MOLECULAR BIOLOGY, 2017, 40 (03) : 656 - 664
  • [30] SEQUENCE SPECIFICITY OF CYTOSINE METHYLATION IN THE DNA OF THE CHINESE-HAMSTER OVARY (CHO-K1) CELL-LINE
    WOODCOCK, DM
    CROWTHER, PJ
    SIMMONS, DL
    COOPER, IA
    BIOCHIMICA ET BIOPHYSICA ACTA, 1984, 783 (03) : 227 - 233