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Effect of low doses of estradiol and tamoxifen on breast cancer cell karyotypes

Título de la revista
Rondón-Lagos, Milena
Rangel, Nelson
Di Cantogno, Ludovica Verdun
Annaratone, Laura
Castellano, Isabella
Russo, Rosalia
Manetta, Tilde
Marchiò, Caterina
Sapino, Anna



ISSN de la revista
Título del volumen
BioScientifica Ltd.


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Evidence supports a role of 17?-estradiol (E2) in carcinogenesis and the large majority of breast carcinomas are dependent on estrogen. The anti-estrogen tamoxifen (TAM) is widely used for both treatment and prevention of breast cancer; however, it is also carcinogenic in human uterus and rat liver, highlighting the profound complexity of its actions. The nature of E2- or TAM-induced chromosomal damage has been explored using relatively high concentrations of these agents, and only some numerical aberrations and chromosomal breaks have been analyzed. This study aimed to determine the effects of low doses of E2 and TAM (10-8 mol L-1 and 10-6 mol L-1 respectively) on karyotypes of MCF7, T47D, BT474, and SKBR3 breast cancer cells by comparing the results of conventional karyotyping and multi-FISH painting with cell proliferation. Estrogen receptor (ER)-positive (+) cells showed an increase in cell proliferation after E2 treatment (MCF7, T47D, and BT474) and a decrease after TAM treatment (MCF7 and T47D), whereas in ER- cells (SKBR3), no alterations in cell proliferation were observed, except for a small increase at 96 h. Karyotypes of both ER+ and ER- breast cancer cells increased in complexity after treatments with E2 and TAM leading to specific chromosomal abnormalities, some of which were consistent throughout the treatment duration. This genotoxic effect was higher in HER2+ cells. The ER-/HER2+ SKBR3 cells were found to be sensitive to TAM, exhibiting an increase in chromosomal aberrations. These in vitro results provide insights into the potential role of low doses of E2 and TAM in inducing chromosomal rearrangements in breast cancer cells. © 2016 Society for Endocrinology Published by Bioscientifica Ltd. Printed in Great Britain.
Palabras clave
Epidermal growth factor receptor 2 , tumor , Estrogen receptor , Progesterone receptor , Tamoxifen , Antiestrogen , Antineoplastic hormone agonists and antagonists , Estradiol , Tamoxifen , Article , Breast cancer cell line , Cell proliferation , Chromosome aberration , Chromosome rearrangement , Controlled study , Genotoxicity , Human , Human cell , In vitro study , Karyotype , Karyotyping , Low drug dose , Mcf 7 cell line , Treatment duration , Breast tumor , Chemically induced , Drug effects , Genetics , Karyotype , Tumor cell line , Antineoplastic agents , Breast neoplasms , Cell line , Cell proliferation , Chromosome aberrations , Estradiol , Estrogen antagonists , Humans , Karyotype , Tamoxifen , Breast cancer cells , Chromosomal abnormalities , Chromosomal instability , Estradiol , Tamoxifen