Overexpression of MDM2 in MCF-7 promotes both growth advantage and p53 accumulation in response to estradiol.
Overexpression of MDM2 in MCF-7 promotes both growth advantage and p53 accumulation in response to estradiol.
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DOI：
10.1111/j.1349-7006.1999.tb00735.x
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发表时间：
1999-03
期刊：
影响因子：
--
通讯作者：
Nozawa Y
中科院分区：
文献类型：
--
作者：
Saji S;Nakashima S;Hayashi S;Toi M;Saji S;Nozawa Y
The overexpression of the oncogene product MDM2 is often observed in human breast cancer cells, especially in estrogen receptor (ER)‐positive ones. To study the role of MDM2 protein in ER‐positive breast cancer, we have established cell lines derived from MCF‐7 which stably express increased and decreased levels of MDM2 by transfection of a mammalian expression vector containing human mdm2 cDNA in sense and antisense orientations, respectively. Interestingly, MDM2 overexpression in MCF‐7 cells afforded a remarkable growth advantage under estradiol (E2)‐sup‐plemented condition. Then, we analyzed the expression of p53, which is an important regulator of growth and the cell cycle. Unexpectedly, the p53 accumulation induced by E2 was remarkably higher in MCF‐7 cells stably overexpressing MDM2 than in the parent MCF‐7 cells. On the other hand, reduction of MDM2 suppressed the E2‐induced increase in p53 protein. Moreover, mdm2 antisense oligonucleotides prevented E2‐induced accumulation of p53. In the steady state, the cellular levels of p53 were also correlated with those of MDM2. These interactions are not consistent with the well‐known role of MDM2, which acts as a negative regulator for p53 by inhibiting its function and promoting its rapid degradation. These results suggest that MDM2 may regulate the expression of p53 in the steady state and in response to E2 in breast cancer cells, and imply a novel and important role of MDM2 during breast carcinogenesis.
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DOI：
10.1007/bf01535205
发表时间：
1987-05-01
期刊：
SOMATIC CELL AND MOLECULAR GENETICS
影响因子：
--
作者：
CAHILLYSNYDER, L;YANGFENG, T;GEORGE, DL
通讯作者：
GEORGE, DL
影响因子：
64.5
作者：
ELDEIRY, WS;TOKINO, T;VOGELSTEIN, B
通讯作者：
VOGELSTEIN, B
影响因子：
11.4
作者：
BARAK, Y;JUVEN, T;OREN, M
通讯作者：
OREN, M
影响因子：
6.8
作者：
Borden, KLB;Freemont, PS
通讯作者：
Freemont, PS
影响因子：
20.3
作者：
MAESTRO, R;GLOGHINI, A;BOIOCCHI, M
通讯作者：
BOIOCCHI, M