Oxysophoridine suppresses the growth of hepatocellular carcinoma in mice: In Vivo and cDNA microarray studies

Xiao-qing Yao; Yun-hui Zhang; Wei Long; Pei-xun Liu

doi:10.1007/s11655-012-1001-6

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Oxysophoridine suppresses the growth of hepatocellular carcinoma in mice: In Vivo and cDNA microarray studies

OriginalPaper | Updated：2021-08-27

- Oxysophoridine suppresses the growth of hepatocellular carcinoma in mice: In Vivo and cDNA microarray studies
- Oxysophoridine suppresses the growth of hepatocellular carcinoma in mice: In Vivo and cDNA microarray studies
- 中国结合医学杂志（英文版） 2012年18卷第3期页码：209-213
- Affiliations：
  
  1. College of Pharmaceutical Science and Technology, Tianjin University,Tianjin,China
  2. Tianjin Chase Sun Pharmaceutical Co., Ltd.,Tianjin,China
  3. Tianjin Key Laboratory of Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College,Tianjin,China
- Author bio：
- Funds：
  
  Supported by Tianjin Key Technology Research & Development Program (No. 07ZCKFSH00200)
- DOI：10.1007/s11655-012-1001-6
  中图分类号：
- 纸质出版日期：2012，
  
  网络出版日期：2012-4-2，
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Yao, Xq., Zhang, Yh., Long, W. et al. Oxysophoridine suppresses the growth of hepatocellular carcinoma in mice: In Vivo and cDNA microarray studies., Chin. J. Integr. Med. 18, 209–213 (2012). https://doi.org/10.1007/s11655-012-1001-6

Xiao-qing Yao, Yun-hui Zhang, Wei Long, et al. Oxysophoridine suppresses the growth of hepatocellular carcinoma in mice: In Vivo and cDNA microarray studies[J]. Chinese Journal of Integrative Medicine, 2012,18(3):209-213.
Yao, Xq., Zhang, Yh., Long, W. et al. Oxysophoridine suppresses the growth of hepatocellular carcinoma in mice: In Vivo and cDNA microarray studies., Chin. J. Integr. Med. 18, 209–213 (2012). https://doi.org/10.1007/s11655-012-1001-6 DOI：

Xiao-qing Yao, Yun-hui Zhang, Wei Long, et al. Oxysophoridine suppresses the growth of hepatocellular carcinoma in mice: In Vivo and cDNA microarray studies[J]. Chinese Journal of Integrative Medicine, 2012,18(3):209-213. DOI： 10.1007/s11655-012-1001-6.

摘要

To observe the in vivo effects of oxysophoridine on hepatocellular carcinoma in mice and to study the related mechanisms. C57BL mice were inoculated with mouse hepatoma H22 cells subcutaneously

then divided into 5 groups (14 per group)

and treated with oxysophoridine (50

100

or 150 mg/kg) or cisplatin (4 mg/kg) for 10 days. Inhibitory rate of tumor

body weight gain

and influence indices on internal organs (liver

spleen and thymus) were evaluated. The differentially expressed genes between the oxysophoridine-treated group

and the control group were analyzed using cDNA microarray and quantitative real-time PCR (qRT-PCR) experiments. Compared with the tumor weight of the control group (2.75±0.66 g)

oxysophoridine significantly suppressed hepatocellular carcinoma growth in mice (P <0.01)

with 0.82±0.36 g

0.57±0.22 g

and 1.22±0.67 g for the tumor weight in the low

moderate

and high dose treatment group

respectively. The moderate dose led to the highest inhibitory rate

79.3%. Observation of body weight gain and influence on three organs showed that compared with cisplatin

oxysophoridine produced fewer side effects in vivo. cDNA microarray and qRT-PCR showed that the most significant differentially expressed genes in the tumor samples of oxysophoridine-treated mice were mostly involved in regulating apoptosis

with the Tnfrsf11b (osteoprotegerin) gene being the most significantly affected. Oxysophoridine was a promising compound for developing drugs against hepatocellular carcinoma

and its anti-hepatoma effect was probably related to osteoprotegerin activation.

Abstract

To observe the in vivo effects of oxysophoridine on hepatocellular carcinoma in mice and to study the related mechanisms. C57BL mice were inoculated with mouse hepatoma H22 cells subcutaneously

then divided into 5 groups (14 per group)

and treated with oxysophoridine (50

100

or 150 mg/kg) or cisplatin (4 mg/kg) for 10 days. Inhibitory rate of tumor

body weight gain

and influence indices on internal organs (liver

spleen and thymus) were evaluated. The differentially expressed genes between the oxysophoridine-treated group

and the control group were analyzed using cDNA microarray and quantitative real-time PCR (qRT-PCR) experiments. Compared with the tumor weight of the control group (2.75±0.66 g)

oxysophoridine significantly suppressed hepatocellular carcinoma growth in mice (P <0.01)

with 0.82±0.36 g

0.57±0.22 g

and 1.22±0.67 g for the tumor weight in the low

moderate

and high dose treatment group

respectively. The moderate dose led to the highest inhibitory rate

79.3%. Observation of body weight gain and influence on three organs showed that compared with cisplatin

with the Tnfrsf11b (osteoprotegerin) gene being the most significantly affected. Oxysophoridine was a promising compound for developing drugs against hepatocellular carcinoma

and its anti-hepatoma effect was probably related to osteoprotegerin activation.

关键词

oxysophoridinehepatocellular carcinomacDNA microarrayqRT-PCRTnfrsf11bosteoprotegerin

Keywords

oxysophoridinehepatocellular carcinomacDNA microarrayqRT-PCRTnfrsf11bosteoprotegerin

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