2006
DOI: 10.1016/j.envres.2005.05.004
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Gene expression profiling reveals novel regulation by bisphenol-A in estrogen receptor-α-positive human cells

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Cited by 58 publications
(54 citation statements)
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“…Estrogen-responsive transcripts involved in growth stimulation, transcription and cell adhesion are listed in Tables III and IV. In agreement with former DNA microarray studies (21)(22)(23)(24)(25)(26)(27)(28)31), the production of TFF1, TFF3 (trefoil factor 3), IGFBP4 (insulin-like growth factor binding protein 4), SDF1, STC2 (stanniocalcin 2), AREG, OLFM1 and OLFML3 (olfactomedin-like 3) was induced upon estrogen treatment. THBS1 (thrombospondin 1) is also upregulated in an estrogendependent manner in T47D cells.…”
Section: Stereotyped Xenostrogenic Transactivationsupporting
confidence: 71%
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“…Estrogen-responsive transcripts involved in growth stimulation, transcription and cell adhesion are listed in Tables III and IV. In agreement with former DNA microarray studies (21)(22)(23)(24)(25)(26)(27)(28)31), the production of TFF1, TFF3 (trefoil factor 3), IGFBP4 (insulin-like growth factor binding protein 4), SDF1, STC2 (stanniocalcin 2), AREG, OLFM1 and OLFML3 (olfactomedin-like 3) was induced upon estrogen treatment. THBS1 (thrombospondin 1) is also upregulated in an estrogendependent manner in T47D cells.…”
Section: Stereotyped Xenostrogenic Transactivationsupporting
confidence: 71%
“…Indeed, the gene expression changes that we observed in response to 17b-estradiol include a large number of transcripts that were previously known to be susceptible to estrogenic regulation, thus substantiating the validity of our transcriptomic analysis. In contrast to previous reports (27)(28)(29)31), we unexpectedly found that the transcriptional machineries of MCF7 and T47D breast cancer cells respond in a very monotonous manner to estrogenic stimuli. Presumably, the differential transcription profiles documented in previous studies arise from dosedependent variations in the magnitude of gene expression, rather than from distinct mechanisms of gene regulation.…”
Section: Discussioncontrasting
confidence: 55%
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“…Genomic DNA was digested and removed using an RNase-Free DNase Kit (Qiagen). First strand cDNA was synthesized using oligo (dT) [12][13][14][15][16][17][18] primer (Invitrogen, Carlsbad, CA, USA) and the Omniscript RT Kit (Qiagen). The synthesized cDNA was thermocycled for PCR amplification with 1 mM each primer and 1.5 U of Taq polymerase.…”
Section: Generation Of Immature Dcs and Their Induction Of Maturationmentioning
confidence: 99%