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Low-dose induction of micronuclei by lindane.

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Low-dose induction of micronuclei by lindane. / Kalantzi, Olga I.; Hewitt, Rebecca; Ford, Kirstie J.; Cooper, Lee J.; Alcock, Ruth E.; Thomas, Gareth O.; Morris, James A.; McMillan, Trevor J.; Jones, Kevin C.; Martin, Francis L.

In: Carcinogenesis, Vol. 25, No. 4, 04.2004, p. 613-622.

Research output: Contribution to journalJournal articlepeer-review

Harvard

Kalantzi, OI, Hewitt, R, Ford, KJ, Cooper, LJ, Alcock, RE, Thomas, GO, Morris, JA, McMillan, TJ, Jones, KC & Martin, FL 2004, 'Low-dose induction of micronuclei by lindane.', Carcinogenesis, vol. 25, no. 4, pp. 613-622. https://doi.org/10.1093/carcin/bgh048

APA

Kalantzi, O. I., Hewitt, R., Ford, K. J., Cooper, L. J., Alcock, R. E., Thomas, G. O., Morris, J. A., McMillan, T. J., Jones, K. C., & Martin, F. L. (2004). Low-dose induction of micronuclei by lindane. Carcinogenesis, 25(4), 613-622. https://doi.org/10.1093/carcin/bgh048

Vancouver

Kalantzi OI, Hewitt R, Ford KJ, Cooper LJ, Alcock RE, Thomas GO et al. Low-dose induction of micronuclei by lindane. Carcinogenesis. 2004 Apr;25(4):613-622. https://doi.org/10.1093/carcin/bgh048

Author

Kalantzi, Olga I. ; Hewitt, Rebecca ; Ford, Kirstie J. ; Cooper, Lee J. ; Alcock, Ruth E. ; Thomas, Gareth O. ; Morris, James A. ; McMillan, Trevor J. ; Jones, Kevin C. ; Martin, Francis L. / Low-dose induction of micronuclei by lindane. In: Carcinogenesis. 2004 ; Vol. 25, No. 4. pp. 613-622.

Bibtex

@article{d75648a5ae2648d1b9802ed366c721db,
title = "Low-dose induction of micronuclei by lindane.",
abstract = "Environmental contaminants possessing hormonal activity have long been suspected of playing a role in cancer causation. What is unclear is whether such agents elicit their effects through genotoxic and/or epigenetic mechanisms. -Hexachlorocyclohexane (-HCH, lindane) was tested in the 10-12–10-4 M range. Chromosomal damage in MCF-7 breast cells and PC-3 prostate cells was assessed using the cytokinesis block micronucleus assay. Micronuclei (MNi) were scored in 1000 binucleate cells per treatment. Cell viability and cell cycle kinetics were also assessed, along with immunocytochemical and quantitative gene expression analyses of CDKN1A (P21WAF1/CIP1), BCL-2 and BAX. Following 24 h treatment, lindane (10-12–10-10 M) induced increases (up to 5-fold) in MNi in both cell lines. Increases in MNi occurred in the absence of DNA single-strand breaks or cytotoxicity and, compared with benzo[a]pyrene and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine, at low concentrations. Lindane induced more MNi than the or {\ss} stereoisomers of HCH. Low dose lindane (10-12–10-10 M) significantly elevated the percentage of MCF-7 cells staining positive for Bcl-2 and of PC-3 cells staining positive for Bax. Only high dose lindane (10-4 M) disrupted cell cycle kinetics with increases in percentage of cells in G1 and decreases in percentage of cells in G2/M. Despite a comparable high dose lindane induction of cell cycle arrest, marked increases in expression of P21WAF1/CIP1 were observed only in MCF-7 cells, although in PC-3 cells a significant increase (P < 0.0005) in the percentage of cells staining positive for p21Waf1/Cip1 was seen. These results suggest that {\textquoteleft}environmental{\textquoteright} concentrations of lindane can induce a number of subtle alterations in breast and prostate cells in the absence of cytotoxicity.",
author = "Kalantzi, {Olga I.} and Rebecca Hewitt and Ford, {Kirstie J.} and Cooper, {Lee J.} and Alcock, {Ruth E.} and Thomas, {Gareth O.} and Morris, {James A.} and McMillan, {Trevor J.} and Jones, {Kevin C.} and Martin, {Francis L.}",
year = "2004",
month = apr,
doi = "10.1093/carcin/bgh048",
language = "English",
volume = "25",
pages = "613--622",
journal = "Carcinogenesis",
issn = "0143-3334",
publisher = "Oxford University Press",
number = "4",

}

RIS

TY - JOUR

T1 - Low-dose induction of micronuclei by lindane.

AU - Kalantzi, Olga I.

AU - Hewitt, Rebecca

AU - Ford, Kirstie J.

AU - Cooper, Lee J.

AU - Alcock, Ruth E.

AU - Thomas, Gareth O.

AU - Morris, James A.

AU - McMillan, Trevor J.

AU - Jones, Kevin C.

AU - Martin, Francis L.

PY - 2004/4

Y1 - 2004/4

N2 - Environmental contaminants possessing hormonal activity have long been suspected of playing a role in cancer causation. What is unclear is whether such agents elicit their effects through genotoxic and/or epigenetic mechanisms. -Hexachlorocyclohexane (-HCH, lindane) was tested in the 10-12–10-4 M range. Chromosomal damage in MCF-7 breast cells and PC-3 prostate cells was assessed using the cytokinesis block micronucleus assay. Micronuclei (MNi) were scored in 1000 binucleate cells per treatment. Cell viability and cell cycle kinetics were also assessed, along with immunocytochemical and quantitative gene expression analyses of CDKN1A (P21WAF1/CIP1), BCL-2 and BAX. Following 24 h treatment, lindane (10-12–10-10 M) induced increases (up to 5-fold) in MNi in both cell lines. Increases in MNi occurred in the absence of DNA single-strand breaks or cytotoxicity and, compared with benzo[a]pyrene and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine, at low concentrations. Lindane induced more MNi than the or ß stereoisomers of HCH. Low dose lindane (10-12–10-10 M) significantly elevated the percentage of MCF-7 cells staining positive for Bcl-2 and of PC-3 cells staining positive for Bax. Only high dose lindane (10-4 M) disrupted cell cycle kinetics with increases in percentage of cells in G1 and decreases in percentage of cells in G2/M. Despite a comparable high dose lindane induction of cell cycle arrest, marked increases in expression of P21WAF1/CIP1 were observed only in MCF-7 cells, although in PC-3 cells a significant increase (P < 0.0005) in the percentage of cells staining positive for p21Waf1/Cip1 was seen. These results suggest that ‘environmental’ concentrations of lindane can induce a number of subtle alterations in breast and prostate cells in the absence of cytotoxicity.

AB - Environmental contaminants possessing hormonal activity have long been suspected of playing a role in cancer causation. What is unclear is whether such agents elicit their effects through genotoxic and/or epigenetic mechanisms. -Hexachlorocyclohexane (-HCH, lindane) was tested in the 10-12–10-4 M range. Chromosomal damage in MCF-7 breast cells and PC-3 prostate cells was assessed using the cytokinesis block micronucleus assay. Micronuclei (MNi) were scored in 1000 binucleate cells per treatment. Cell viability and cell cycle kinetics were also assessed, along with immunocytochemical and quantitative gene expression analyses of CDKN1A (P21WAF1/CIP1), BCL-2 and BAX. Following 24 h treatment, lindane (10-12–10-10 M) induced increases (up to 5-fold) in MNi in both cell lines. Increases in MNi occurred in the absence of DNA single-strand breaks or cytotoxicity and, compared with benzo[a]pyrene and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine, at low concentrations. Lindane induced more MNi than the or ß stereoisomers of HCH. Low dose lindane (10-12–10-10 M) significantly elevated the percentage of MCF-7 cells staining positive for Bcl-2 and of PC-3 cells staining positive for Bax. Only high dose lindane (10-4 M) disrupted cell cycle kinetics with increases in percentage of cells in G1 and decreases in percentage of cells in G2/M. Despite a comparable high dose lindane induction of cell cycle arrest, marked increases in expression of P21WAF1/CIP1 were observed only in MCF-7 cells, although in PC-3 cells a significant increase (P < 0.0005) in the percentage of cells staining positive for p21Waf1/Cip1 was seen. These results suggest that ‘environmental’ concentrations of lindane can induce a number of subtle alterations in breast and prostate cells in the absence of cytotoxicity.

U2 - 10.1093/carcin/bgh048

DO - 10.1093/carcin/bgh048

M3 - Journal article

VL - 25

SP - 613

EP - 622

JO - Carcinogenesis

JF - Carcinogenesis

SN - 0143-3334

IS - 4

ER -