Integrative analyses of gene expression and DNA methylation profiles in breast cancer cell line models of tamoxifen-resistance indicate a potential role of cells with stem-like properties
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Integrative analyses of gene expression and DNA methylation profiles in breast cancer cell line models of tamoxifen-resistance indicate a potential role of cells with stem-like properties. / Lin, Xue; Li, Jian; Yin, Guangliang; Zhao, Qian; Elias, Daniel; Lykkesfeldt, Anne; Stenvang, Jan; Brünner, Nils; Wang, Jun; Yang, Huanming; Bolund, Lars; Ditzel, Henrik Jørn.
In: Breast cancer research : BCR, Vol. 15, No. 6, R119, 2013.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Integrative analyses of gene expression and DNA methylation profiles in breast cancer cell line models of tamoxifen-resistance indicate a potential role of cells with stem-like properties
AU - Lin, Xue
AU - Li, Jian
AU - Yin, Guangliang
AU - Zhao, Qian
AU - Elias, Daniel
AU - Lykkesfeldt, Anne
AU - Stenvang, Jan
AU - Brünner, Nils
AU - Wang, Jun
AU - Yang, Huanming
AU - Bolund, Lars
AU - Ditzel, Henrik Jørn
PY - 2013
Y1 - 2013
N2 - Development of resistance to tamoxifen is an important clinical issue in the treatment of breast cancer. Tamoxifen resistance may be the result of acquisition of epigenetic regulation within breast cancer cells, such as DNA methylation, resulting in changed mRNA expression of genes pivotal for estrogen-dependent growth. Alternatively, tamoxifen resistance may be due to selection of pre-existing resistant cells, or a combination of the two mechanisms.
AB - Development of resistance to tamoxifen is an important clinical issue in the treatment of breast cancer. Tamoxifen resistance may be the result of acquisition of epigenetic regulation within breast cancer cells, such as DNA methylation, resulting in changed mRNA expression of genes pivotal for estrogen-dependent growth. Alternatively, tamoxifen resistance may be due to selection of pre-existing resistant cells, or a combination of the two mechanisms.
U2 - 10.1186/bcr3588
DO - 10.1186/bcr3588
M3 - Journal article
C2 - 24355041
VL - 15
JO - Breast Cancer Research
JF - Breast Cancer Research
SN - 1465-5411
IS - 6
M1 - R119
ER -
ID: 98037889