Journal of Capital Medical University ›› 2019, Vol. 40 ›› Issue (2): 237-243.doi: 10.3969/j.issn.1006-7795.2019.02.016

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Progesterone receptor membrane component 1 increases hormone induced proliferation of breast cancer cells——E2 vs sequential combination vs continuous combination

Li Xue1, Ruan Xiangyan1,2, Gu Muqing1, Cai Guiju1, Zhao Yue1, Alfred O. Meuck1,2   

  1. 1. Department of Endocrinology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing 100026, China;
    2. Department for Women's Health, University Women's Hospital and Research Center for Women's Health, University of Tuebingen, Tuebingen D-72076, Germany
  • Received:2019-01-04 Online:2019-03-21 Published:2019-04-15
  • Supported by:
    This study was supported by National Natural Science Foundation of China (81671411), Natural Science Foundation of Beijing (7162062), Beijing Nova Program Interdisciplinary Cooperation Projects (Z161100004916045), Beijing Municipality Health Technology Highlevel Talent (2014-2-016), Beijing Municipal Administration of Hospitals' Ascent Plan(DFL20181401),The First Batch of Beijing Maternal and Child Health Specialist Demonstration units "Menopausal Health Specialist"(2018.01-2020.12).

Abstract: Objective To investigate the effect of progesterone receptor membrane component 1 (PGRMC1) on the risk of hormone induced breast cancer, and compare the effects of different treatment regimens:estradiol (E2)/sequential combination/continuous combination(E2/DRSP、E2/NET) on breast cancer proliferation. Methods After stabilized transfection by lipofection, T47D cells transfected with vector(T47D-HA-vector) or PGRMC1(T47D-HA-PGRMC1) were stimulated with E2 alone (0.1, 0.01, 0.001 nmol/L), or sequential/continuous combination. CCK-2 method was performed to measure cell proliferation. Results When treated with E2 (0.001, 0.01, 0.1 nmol/L) alone, T47D-HA-vector cells did not show significant proliferation (P>0.05). At concentration of 0.1 nmol/L, T47D-HA-PGRMC1 cell reached a significant increase in cell proliferation compared with the control group (56%, P<0.05) and compared with T47D-HA-vector group (36%, P<0.05); when treated with sequential combination, T47D-HA-PGRMC1 cell under E2/NET treatment (E2=0.001 nmol/L) showed a significant increase in cell proliferation compared with the control group (82%, P<0.05) and T47D-HA-vector group (63%, P<0.05). Under the same stimulation, when the concentration of E2 reached 0.1 nmol/L, T47D-HA-vector showed a significant increase compared with the control group (37%, P<0.05), and for the T47D-HA-PGRMC1 cell line, when under E2/drospirenone (DRSP) or E2/norethisterone (NET) stimulation (E2=0.1 nmol/L), a significant increase compared with the control group (105%, 170%, P<0.05) and T47D-HA-vector group (84%, 133%, P<0.05) was observed; when treated with the continuous combination, the T47D-HA-PGRMC1 cell line showed a significant increase in cell proliferation under E2/DRSP or E2/NET stimulation (E2=0.001 nmol/L) compared with the control group (77%, 158%, P<0.05) and T47D-HA-vector group(60%, 136%, P<0.05). The T47D-HA-vector cell line showed a significant increase under E2/NET stimulation (E2=0.1 nmol/L) compared with the control group (44%, P<0.05), and the T47D-HA-PGRMC1 cell line under E2/DRSP or E2/NET stimulation (E2=0.1 nmol/L) showed a significant increase in cell proliferation compared with the control group (129%, 174%, P<0.05) and T47D-HA-vector group (97%, 131%, P<0.05). Conclusion PGRMC1 can significantly promote the proliferation of breast cancer cells induced by sequential/continuous combination. Compared with the sequential combination, the continuous combination promoted a higher proliferation of T47D.

Key words: progesterone receptor membrane component 1, sequential combination, continuous combination, breast cancer, cell proliferation

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