Label-free proteomics uncovers SMC1A expression is Down-regulated in AUB-E
Abstract Background While heavy menstrual bleeding (HMB) is a prevalent symptom among women with abnormal uterine bleeding caused by endometrial disorder (AUB-E) seeking gynecologic care, the primary endometrial disorder remains poorly understood. Methods Five human endometrial samples from women wi...
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doaj-d881a585825944a7a32bc3da361ed87e2021-03-11T11:27:48ZengBMCReproductive Biology and Endocrinology1477-78272021-03-0119111010.1186/s12958-021-00713-4Label-free proteomics uncovers SMC1A expression is Down-regulated in AUB-EYingxian Jia0Jie Luo1Yibing Lan2Chunming Li3Linjuan Ma4Xiaoming Zhu5Fei Ruan6Jianhong Zhou7Women’s Hospital, School of Medicine, Zhejiang UniversityWomen’s Hospital, School of Medicine, Zhejiang UniversityWomen’s Hospital, School of Medicine, Zhejiang UniversityWomen’s Hospital, School of Medicine, Zhejiang UniversityWomen’s Hospital, School of Medicine, Zhejiang UniversityWomen’s Hospital, School of Medicine, Zhejiang UniversityWomen’s Hospital, School of Medicine, Zhejiang UniversityWomen’s Hospital, School of Medicine, Zhejiang UniversityAbstract Background While heavy menstrual bleeding (HMB) is a prevalent symptom among women with abnormal uterine bleeding caused by endometrial disorder (AUB-E) seeking gynecologic care, the primary endometrial disorder remains poorly understood. Methods Five human endometrial samples from women with AUB-E and the age-matched healthy women were selected, respectively. Proteins from the samples were analyzed by a linear ion trap (LTQ)-Orbitrap Elite mass spectrometer based label-free proteomic approach. The purpose protein was validated by western blot and immunohistochemistry staining. Results A total of 2353 protein groups were quantified under highly stringent criteria with a false discovery rate of < 1% for protein groups, and 291 differentially expressed proteins were significantly changed between the two groups. The results showed that the down-regulation of structural maintenance of chromosomes protein 1A (SMC1A) in AUB-E patients. Next, this change in the glandular epithelial cells was validated by immunohistochemistry. Conclusion The results indicated a novel mechanism for the cause of AUB-E, as down-expression SMC1A potentially regulated the cell cycle progression in endometrial glandular epithelium further led to bleeding.https://doi.org/10.1186/s12958-021-00713-4Abnormal uterine bleedingHuman endometriumProteomic analysisPrimary endometrial disorder |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yingxian Jia Jie Luo Yibing Lan Chunming Li Linjuan Ma Xiaoming Zhu Fei Ruan Jianhong Zhou |
spellingShingle |
Yingxian Jia Jie Luo Yibing Lan Chunming Li Linjuan Ma Xiaoming Zhu Fei Ruan Jianhong Zhou Label-free proteomics uncovers SMC1A expression is Down-regulated in AUB-E Reproductive Biology and Endocrinology Abnormal uterine bleeding Human endometrium Proteomic analysis Primary endometrial disorder |
author_facet |
Yingxian Jia Jie Luo Yibing Lan Chunming Li Linjuan Ma Xiaoming Zhu Fei Ruan Jianhong Zhou |
author_sort |
Yingxian Jia |
title |
Label-free proteomics uncovers SMC1A expression is Down-regulated in AUB-E |
title_short |
Label-free proteomics uncovers SMC1A expression is Down-regulated in AUB-E |
title_full |
Label-free proteomics uncovers SMC1A expression is Down-regulated in AUB-E |
title_fullStr |
Label-free proteomics uncovers SMC1A expression is Down-regulated in AUB-E |
title_full_unstemmed |
Label-free proteomics uncovers SMC1A expression is Down-regulated in AUB-E |
title_sort |
label-free proteomics uncovers smc1a expression is down-regulated in aub-e |
publisher |
BMC |
series |
Reproductive Biology and Endocrinology |
issn |
1477-7827 |
publishDate |
2021-03-01 |
description |
Abstract Background While heavy menstrual bleeding (HMB) is a prevalent symptom among women with abnormal uterine bleeding caused by endometrial disorder (AUB-E) seeking gynecologic care, the primary endometrial disorder remains poorly understood. Methods Five human endometrial samples from women with AUB-E and the age-matched healthy women were selected, respectively. Proteins from the samples were analyzed by a linear ion trap (LTQ)-Orbitrap Elite mass spectrometer based label-free proteomic approach. The purpose protein was validated by western blot and immunohistochemistry staining. Results A total of 2353 protein groups were quantified under highly stringent criteria with a false discovery rate of < 1% for protein groups, and 291 differentially expressed proteins were significantly changed between the two groups. The results showed that the down-regulation of structural maintenance of chromosomes protein 1A (SMC1A) in AUB-E patients. Next, this change in the glandular epithelial cells was validated by immunohistochemistry. Conclusion The results indicated a novel mechanism for the cause of AUB-E, as down-expression SMC1A potentially regulated the cell cycle progression in endometrial glandular epithelium further led to bleeding. |
topic |
Abnormal uterine bleeding Human endometrium Proteomic analysis Primary endometrial disorder |
url |
https://doi.org/10.1186/s12958-021-00713-4 |
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