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Dual control of kidney nourishing therapy on CyclinD-CDK4/6 signal pathway of cell reproductive cycles in Lewis-bearing mice with cyclophosphamide-induced mye1osuppression.
Gu Xian 1,Xu Zhen-ye 2 *
1.Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, ShangHai 200126
2.Longhua Hospital Affiliated To Shanghai University of TCM
*Correspondence author
#Submitted by
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Funding: 高等学校博士学科点专项科研基金(No.20093107110004)
Opened online:25 December 2012
Accepted by: none
Citation: Gu Xian,Xu Zhen-ye.Dual control of kidney nourishing therapy on CyclinD-CDK4/6 signal pathway of cell reproductive cycles in Lewis-bearing mice with cyclophosphamide-induced mye1osuppression.[OL]. [25 December 2012] http://en.paper.edu.cn/en_releasepaper/content/4505679
 
 
Background:This study investigated the dual control mechanism of kidney nourishing therapy modulating the cell cycle in Lewis-bearing mice with cyclophosphamide induced myelosuppression. Methods: Thirty Lewis-bearing mice were randomly grouped into an untreated group, control group, and treated group. Both treated and untreated groups were intraperitoneally injected with cyclophosphamide to produce a myelosuppression model. Mice in the treated group were fed with theShuanghuangShengbaigranule (40 g/day) for 6 consecutive days. Standard blood tests and the count of bone marrow nuclear cells were performed, and the cell reproductive cycles of bone marrow and tumorswere measured in these mice. In addition, the western blot approach was used to measure the upstream activating signals of CyclinD-CDK4/6 such as c-Myc and CDC25A, the upstream suppression signals such as p16INK4a and p15INK4b, and the expression of downstream activated signals such as Rb, pRB, and E2F. All of the tested results were validated by reverse transcription quantitative real-time polymerase chain reaction. Results: The results showed that the ShuanghuangShengbaigranule could elevate the count of leukocyte and bone marrow nuclear cells of Lewis-bearing mice with cyclophosphamide induced myelosuppression. It could also stimulate bone marrow cells to move from G0/G1 phases to S phase, accelerating the progress of the cell reproductive cycle and increasing the cell proliferation index. Simultaneously, the ShuanghuangShengbaigranule could also suppress cancer cells moving from G0/G1 phase to S phase, reducing the proliferation index. The tumor weight of Lewis-bearing mice in the treated group was much less than those of the control group. Expression levels of c-Myc, CDC25A, Rb, pRb, and E2F of bone marrow in ShuanghuangShengbaigranule-treated mice was higher compared to the control group, whereas they were lower in the cancer cells. Conclusion: The experimental results demonstrate that the ShuanghuangShengbaigranule has dual control on the cell reproductive cycles in cancer cells and bone marrow nuclear cells in Lewis-bearing mice.
Keywords:kidney nourishing therapy; CyclinD-CDK4/6; c-Myc; CDC25A; p16INK4a; p15INK4b; Rb; pRb; E2F
 
 
 

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