Chinese Journal of Tissue Engineering Research ›› 2011, Vol. 15 ›› Issue (15): 2833-2837.doi: 10.3969/j.issn.1673-8225.2011.15.042

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Bioinformatics analysis of genes expression profiles of postmenopausal osteoporosis with Kidney Yin deficiency

Xie Li-hua, Zhao Yi-peng, Chen Ke, Lai Yu-lian, Ge Ji-rong   

  1. Department of Basic Theory of Traditional Chinese Medicine, Fujian Institute of Chinese Medicine, Fuzhou  350003, Fujian Province, China
  • Received:2010-12-17 Revised:2011-03-10 Online:2011-04-09 Published:2013-11-06
  • Contact: Ge Ji-rong, Doctor, Associate researcher, Department of Basic Theory of Traditional Chinese Medicine, Fujian Institute of Chinese Medicine, Fuzhou 350003, Fujian Province, China gjrrjgcy@sohu.com
  • About author:Xie Li-hua★, Master, Assistant researcher, Department of Basic Theory of Traditional Chinese Medicine, Fujian Institute of Chinese Medicine, Fuzhou 350003, Fujian Province, China xlhat@163.com
  • Supported by:

    the Natural Science Foundation of Fujian Province, No. 2009J01160*; the Independent Topic Selection of Commonweal Scientific Institutes of Fujian Provincial Science and Technology Commission, No. 2009R10007-3*

Abstract:

BACKGROUND: Gene differential expression exists in various types of postmenopausal osteoporosis, but its genomics mechanism has not been studied and reported.
OBFECTIVE: Through analyzing the gene expression spectrum’s difference, to investigate characteristics of genes expression profiles of postmenopausal osteoporosis with Kidney Yin deficiency.
METHODS: By TCM syndrome, 13 patients with postmenopausal osteoporosis were randomly divided into three groups: kidney Yin deficiency (n=4), kidney Yang deficiency (n=3), non-kidney deficiency (n=3), another 3 healthy postmenopausal women also were selected as control group. Human gene expression microarrays were applied to explore gene expression spectrum's difference of the groups. Kidney Yin deficiency group was compared with other three groups respectively. The genes with common significant difference were studied by Go and Pathway analysis.
RESULTS AND CONCLUSION: Compared with control group, kidney Yang deficiency and non-kidney deficiency groups, there were 197, 354 and 54 genes expressed differentially in the kidney Yin deficiency group. Nine genes were expressed differentially among kidney Yin deficiency group with other three groups: PROK2, ASB1, MUC12, GSTM5, CLCF1, GPR27, C3orf35 and unknown genes chr3:113822408-11382234, chr18:34851804-34851745. Compared with control group, GSTM5 and MUC12 showed up-regulated expression, GPR27, C3orf35, ASB1, CLCF1 and PROK2 showed down-regulated expression. The pathway analysis showed GSTM5 was involved in glutathione metabolism, and CLCF1 was involved in cytokine-cytokine receptor interaction and Jak-STAT signaling. The pathogenesis of postmenopausal osteoporosis with kidney Yin deficiency is associated with the genes expression of GPR27, ASB1, PROK2, CLCF1 and GSTM5, and it has association with glutathione metabolism pathway, cytokine-cytokine receptor interaction pathway and Jak-STAT signaling pathway.

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