TY - JOUR
T1 - Microtubule disruption induced by estradiol in estrogen receptor-positive and -negative human breast cancer cell lines
AU - Aizu-yokota, Eriko
AU - Ichinoseki, Ken
AU - Sato, Yoshihiro
N1 - Funding Information:
The authors would like to thank Professor Dr Manfred Metzler (University of Kaiserslautern, Germany) for his thoughtful review of the manuscript. We thank Miss Akiko Kuroda for technical assistance. This study was supported in part by a grant from the Nishi Cancer Research Fund.
PY - 1994/9
Y1 - 1994/9
N2 - Effects of estrogens on the cytoplasmic microtubule network were examined by the indirect immunofluorescence method using anti-β-tubulin antibody. Estradiol, a naturally occurring estrogen, decreased the amount of cytoplasmic microtubule fibers during interphase in the human breast cancer cell lines MCF-7 and MDA-MB-231. Since MDA-MB-231 is an estrogen receptor-negative cell line, estradiol-induced microtubule disruption seems to be independent of estradiol binding to receptors. The effective concentration of estradiol required for induction of microtubule disruption in 50% of the cells (EC50) was 81 μM for MCF-7 cells and 82 μM for MDA-MB-231 cells. A synthetic estrogen, diethylstilbestrol, also induced a decrease in microtubule fibers, with an EC50 value of 48 μM for MCF-7 cells and 50 μM for MDA-MB-231 cells. When estrogentreated and microtubule-depolymerized cells were washed and the medium was replaced with fresh, intracellular microtubule networks reappeared within 3 h. When MCF-7 cells were cultured for 4 days with estradiol (50 μM), cell growth was completely inhibited. However, estrone affected the microtubule network and cell proliferation only slightly. These results suggest that estradiol-induced microtubule disruption is closely related to its inhibitory effect on cell growth.
AB - Effects of estrogens on the cytoplasmic microtubule network were examined by the indirect immunofluorescence method using anti-β-tubulin antibody. Estradiol, a naturally occurring estrogen, decreased the amount of cytoplasmic microtubule fibers during interphase in the human breast cancer cell lines MCF-7 and MDA-MB-231. Since MDA-MB-231 is an estrogen receptor-negative cell line, estradiol-induced microtubule disruption seems to be independent of estradiol binding to receptors. The effective concentration of estradiol required for induction of microtubule disruption in 50% of the cells (EC50) was 81 μM for MCF-7 cells and 82 μM for MDA-MB-231 cells. A synthetic estrogen, diethylstilbestrol, also induced a decrease in microtubule fibers, with an EC50 value of 48 μM for MCF-7 cells and 50 μM for MDA-MB-231 cells. When estrogentreated and microtubule-depolymerized cells were washed and the medium was replaced with fresh, intracellular microtubule networks reappeared within 3 h. When MCF-7 cells were cultured for 4 days with estradiol (50 μM), cell growth was completely inhibited. However, estrone affected the microtubule network and cell proliferation only slightly. These results suggest that estradiol-induced microtubule disruption is closely related to its inhibitory effect on cell growth.
UR - http://www.scopus.com/inward/record.url?scp=0028070218&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0028070218&partnerID=8YFLogxK
U2 - 10.1093/carcin/15.9.1875
DO - 10.1093/carcin/15.9.1875
M3 - Article
C2 - 7923580
AN - SCOPUS:0028070218
SN - 0143-3334
VL - 15
SP - 1875
EP - 1879
JO - Carcinogenesis
JF - Carcinogenesis
IS - 9
ER -