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Gynecology Department of Traditional Chinese Medicine, Clinical Medical College, Chengdu University of Traditional Chinese Medicine,Chengdu,China
纸质出版日期:2018,
网络出版日期:2017-1-24,
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Wen, Y., Wang, Y., Feng, Tt. et al. Differential Proteomics Analysis of Endometriosis in Blood Stasis Syndrome., Chin. J. Integr. Med. 24, 925–929 (2018). https://doi.org/10.1007/s11655-017-2401-4
Yi Wen, Yan Wang, Ting-ting Feng, et al. Differential Proteomics Analysis of Endometriosis in Blood Stasis Syndrome[J]. Chinese Journal of Integrative Medicine, 2018,24(12):925-929.
Wen, Y., Wang, Y., Feng, Tt. et al. Differential Proteomics Analysis of Endometriosis in Blood Stasis Syndrome., Chin. J. Integr. Med. 24, 925–929 (2018). https://doi.org/10.1007/s11655-017-2401-4 DOI:
Yi Wen, Yan Wang, Ting-ting Feng, et al. Differential Proteomics Analysis of Endometriosis in Blood Stasis Syndrome[J]. Chinese Journal of Integrative Medicine, 2018,24(12):925-929. DOI: 10.1007/s11655-017-2401-4.
To investigate the innate characters of 3 endometriosis (EMT) syndromes
blood stasis (BS)
qi stagnation and blood stasis (QSBS) as well as Shen (Kidney) deficiency and blood stasis (KDBS) in terms of proteomics
lay a molecular biological basis for the differentiation of various blood stasis syndromes of EMT
establish a EMT microscopic syndrome differentiation and diagnosis system in terms of proteomics
discover the evolution principles and therapeutic targets of these EMT syndromes
and search their signifificant molecular markers and genetic intervention targets. Six specimens from the ectopic and entopic endometrium tissues of patients with EMT in each syndrome
BS
QSBS as well as KDBS
in the early proliferative phase of the menstrual cycle
and 6 specimens from normal endometrium tissues in the early proliferative phase of the menstrual cycle were obtained. Three groups were formed in each syndrome by mixing two random specimens in equal amount
and then their respective two-dimensional electrophoresis graphs were obtained after total protein extraction. Finally
the detected differences in protein expression were identifified through matrix-assisted laser desorption Ionization-time of flflight mass spectrometry (MALDI-TOF/MS) and protein database. The results of differential proteins expressed in each syndrome were shown as follows: BS syndrome had 2 differential proteins in entopic endometrium and 1 differential protein in ectopic endometrium; KDBS syndrome had 3 in entopic endometrium and 3 in ectopic endometrium; and QSBS syndrome had 3 in entopic endometrium and 4 in ectopic endometrium. It was found out that annexin was highly expressed in both entopic and ectopic endometrium of KDBS syndrome; and myosin light chain 3 was highly expressed in both entopic and ectopic endometrium of QSBS syndrome. There are differential protein expressions among the 3 EMT syndromes
which might be the inner origin of syndrome characters
and these differential proteins might be the candidate biomarkers for the pathogenesis of various EMT syndromes.
To investigate the innate characters of 3 endometriosis (EMT) syndromes
blood stasis (BS)
qi stagnation and blood stasis (QSBS) as well as Shen (Kidney) deficiency and blood stasis (KDBS) in terms of proteomics
lay a molecular biological basis for the differentiation of various blood stasis syndromes of EMT
establish a EMT microscopic syndrome differentiation and diagnosis system in terms of proteomics
discover the evolution principles and therapeutic targets of these EMT syndromes
and search their signifificant molecular markers and genetic intervention targets. Six specimens from the ectopic and entopic endometrium tissues of patients with EMT in each syndrome
BS
QSBS as well as KDBS
in the early proliferative phase of the menstrual cycle
and 6 specimens from normal endometrium tissues in the early proliferative phase of the menstrual cycle were obtained. Three groups were formed in each syndrome by mixing two random specimens in equal amount
and then their respective two-dimensional electrophoresis graphs were obtained after total protein extraction. Finally
the detected differences in protein expression were identifified through matrix-assisted laser desorption Ionization-time of flflight mass spectrometry (MALDI-TOF/MS) and protein database. The results of differential proteins expressed in each syndrome were shown as follows: BS syndrome had 2 differential proteins in entopic endometrium and 1 differential protein in ectopic endometrium; KDBS syndrome had 3 in entopic endometrium and 3 in ectopic endometrium; and QSBS syndrome had 3 in entopic endometrium and 4 in ectopic endometrium. It was found out that annexin was highly expressed in both entopic and ectopic endometrium of KDBS syndrome; and myosin light chain 3 was highly expressed in both entopic and ectopic endometrium of QSBS syndrome. There are differential protein expressions among the 3 EMT syndromes
which might be the inner origin of syndrome characters
and these differential proteins might be the candidate biomarkers for the pathogenesis of various EMT syndromes.
endometriosisBlood Stasis Syndromeproteomicstwo-dimensional electrophoresismass spectrum
endometriosisBlood Stasis Syndromeproteomicstwo-dimensional electrophoresismass spectrum
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