Study of the correlation between the colorectal cancer Chinese medicine syndrome types and (excision repair cross-complementing 1, ERCC1) gene polymorphisms.
- Author:
Tong-Jian CUI
1
;
Yi-Qian CHEN
;
Yong-Mei DAI
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Aged; Colorectal Neoplasms; diagnosis; genetics; DNA-Binding Proteins; genetics; Endonucleases; genetics; Female; Genotype; Humans; Male; Medicine, Chinese Traditional; Middle Aged; Polymorphism, Genetic; Yang Deficiency; Yin Deficiency
- From: Chinese Journal of Integrated Traditional and Western Medicine 2012;32(5):628-632
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo explore the correlation between excision repair cross-complementing 1 (ERCC1) C8092A and C19007T gene polymorphisms and different Chinese medicine (CM) syndrome types of colorectal cancer (CC).
METHODSNinety-nine patients with CC were syndrome typed as dampness-heat accumulation syndrome, qi stagnation with blood stasis syndrome, Pi-Shen yang deficiency syndrome, and Gan-Shen yin deficiency syndrome. The gene polymorphisms of excision repair cross-complementing 1 (ERCC1) C8092A and C19007T in different CM syndrome types of CC were examined by polymorphisms chain reaction amplification and direct sequencing, and analyzed statistically.
RESULTSThe frequencies of C8092A genotype and allele in different CM syndrome types had no statistical difference (P > 0.05). The frequencies of C19007T genotype and allele in different CM syndrome types had statistical difference (P < 0.05). Of them, there was no statistical difference in the frequencies between dampness-heat accumulation syndrome and qi stagnation with blood stasis syndrome, or between Pi-Shen yang deficiency syndrome and Gan-Shen yin deficiency syndrome (P > 0.05). There was statistical difference between dampness-heat accumulation syndrome and Pi-Shen yang deficiency syndrome as well as Gan-Shen yin deficiency syndrome (P < 0.05). There was statistical difference between qi stagnation with blood stasis syndrome and Pi-Shen yang deficiency syndrome as well as Gan-Shen yin deficiency syndrome (P < 0.05).
CONCLUSIONERCC1 C19007T gene polymorphisms might be associated with CM syndrome types of CC, which needed to be further studied.