Effects of modified Shu-Gan-Liang-Xue decoction combined with anastrozole on osteoblastic proliferation and differentiation of MC3T3-E1 cells

被引:7
|
作者
Zhou, Fei [1 ]
Han, Shuyan [1 ]
Zhou, Ning [1 ]
Zheng, Wenxian [1 ]
Li, Pingping [1 ]
机构
[1] Peking Univ Canc Hosp & Inst, Minist Educ, Key Lab Carcinogenesis & Tradit Res, Dept Integrated Tradit Chinese & Western Med, Beijing 100142, Peoples R China
基金
北京市自然科学基金;
关键词
modified Shu-Gan-Liang-Xue decoction; osteoblast-like cell; alkaline phosphatase; osteocalcin; mineralization; EARLY BREAST-CANCER; POSTMENOPAUSAL WOMEN; AROMATASE INHIBITORS; BONE LOSS; ZOLEDRONIC ACID; BIOCHEMICAL MARKERS; GENE-EXPRESSION; IN-VIVO; ZO-FAST; THERAPY;
D O I
10.3892/mmr.2014.2962
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aromatase inhibitors (AIs) are widely used in the treatment of hormone-dependent breast cancer and as a result, aromatase inhibitor-associated bone loss (AIBL) has become a major concern amongst patients receiving AT treatment. Modified Shu-Gan-Liang-Xue decoction (mSGLXD), a clinical prescription, has been used for ameliorating AIBL in patients with breast cancer for decades and has achieved good clinical efficacy. However, the mechanism underlying how mSGLXD influences bone homeostasis and alleviates AIBL has remained elusive. In the present study, mSGLXD was supplemented with Rhizoma Drynariae containing phytoestrogens, and the safety of mSGLXD was evaluated. mSGLXD did not possess estrogenic activity and significantly inhibited the proliferation of estrogen receptor-positive breast cancer cell line MCF-7, which suggested that mSGLXD was safe for postmenopausal patients with breast cancer. Subsequently, the effects of mSGLXD alone or in combination with anastrozole on osteoblastic MC3T3-E1 cell proliferation and differentiation were investigated. Cell counting kit-8, reverse transcription-polymerase chain reaction and biochemical methods, such as ELISA and alizarin red S staining, were used in the present study. It was revealed that mSGLXD not only stimulated MC3T3-E1 cell proliferation, but also upregulated alkaline phosphatase and osteocalcin gene and protein expression levels. High concentrations of anastrozole (10 or 100 mu mol/l) markedly inhibited MC3T3-E1 cell proliferation, but this inhibitory effect was attenuated by mSGLXD. Furthermore, mSGLXD increased MC3T3-E1 cell mineralization following beta-glycerophosphate and ascorbic acid induction. Therefore, the results of the present study suggested that mSGLXD may be a promising adjuvant therapy, with high safety and efficacy, for the prevention and treatment of AIBL in patients with breast cancer who receive AT treatment.
引用
收藏
页码:1639 / 1646
页数:8
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