Effects of estrogens and antiestrogens on estrogen receptor dynamics and the induction of progesterone receptor in MCF-7 human breast cancer cells.

己烯雌酚 雌激素受体 孕酮受体 内分泌学 MCF-7型 内科学 化学 雌激素 受体 雌激素受体α 抗雌激素 乳腺癌 癌症 生物 医学 人体乳房
作者
Richard L. Eckert,Benita S. Katzenellenbogen
出处
期刊:PubMed 卷期号:42 (1): 139-44 被引量:212
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Abstract Antiestrogens appear to be useful in the treatment of endocrine-responsive breast cancers in humans. In an attempt to understand their interactions with breast cancer cells, we have examined the effects of estrogens (estradiol and diethylstilbestrol), and antiestrogens with a range of affinities for estrogen receptor (ER), on intracellular ER dynamics and biological response (progesterone receptor) induction in MCF-7 human breast cancer cells. The triphenylethylene antiestrogens studied are α-{ p -[2-(1-pyrrolidino)ethoxy]phenyl}-4-methoxy-α′-nitrostilbene (CI628), α-{ p -[2-(1-pyrrolidino)ethoxy]phenyl}-4-hydroxy-α′-nitrostilbene (CI628M), cis -{3-[p-(1,2,3,4,-tetrahydro-6-methoxy-2-phenyl-1-naphthyl)phenoxy]-1,2-propanediol} (U23,469), and cis -{3-[p-(1,2,3,4-tetrahydro-6-hydroxy-2-phenyl-1-naphthyl)phenoxy]-1,2,propanediol} (U23,469M). The relative binding affinities of the antiestrogens CI628, CI628M, U23,469, and U23,469M for cytoplasmic ER (ERC) were 1.0, 17, 0.04, and 34%, respectively, in which the affinity of estradiol is considered 100%. Receptor-saturating concentrations of CI628, CI628M, estradiol, and diethylstilbestrol (200, 10, 10, and 10 nM, respectively) caused complete ERC depletion and peak nuclear ER accumulation within 1 hr. The nuclear receptor (ERN) sites declined thereafter and stabilized at near-control levels (1.2 pmol ERN per mg DNA) by 2 to 5 hr, resulting in a new loss (processing) of approximately 50% of total cellular ER. In contrast, U23,469 (2000 nM) promoted complete depletion of ERC and quantitative accumulation as ERN within 5 min, but the total ER content remained constant thereafter (no processing). U23,469M (60 nM) promoted complete ERC depletion and quantitative nuclear accumulation, but the number of ERN sites subsequently declined slowly to reach the control level by Day 5. Among these compounds, estradiol and diethylstilbestrol (0.1 to 1000 nM) promoted a 600% increase in cytoplasmic progesterone receptor (5 days, control = 0.2 pmol/mg DNA). Cl628M and U23,469M (1 to 10 nM) produced only a 300% increase, and U23,469 and Cl628 (0.1 to 1000 nM) did not promote any increase. These results indicate that: ( a ) ER translocation to the nucleus and progesterone receptor induction appear to be related to ligand affinity; ( b ) antiestrogens can differ substantially from one another in their dynamics of interaction with ER and in their abilities to stimulate increases in cellular progesterone receptor; ( c ) processing of ER by antiestrogens such as CI628 does not ensure subsequent induction of progesterone receptor; and ( d ) an apparently complex relationship exists between the presence and duration of hormone receptor complexes in the nucleus and the induction of progesterone receptor in MCF-7 cells. Since all four antiestrogens inhibit MCF-7 cell growth but differ in their ability to increase cellular progesterone receptor levels, these studies indicate that growth and progesterone receptor induction are phenomena that are independently modulated by antiestrogens in these human breast cancer cells.

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