Proteomics of Uterosacral Ligament Connective Tissue from Women with and without Pelvic Organ Prolapse.

iTRAQ analysis ingenuity pathway analysis molecular pathogenesis musculoskeletal system pelvic organ prolapse reproductive system uterosacral ligament

Journal

Proteomics. Clinical applications
ISSN: 1862-8354
Titre abrégé: Proteomics Clin Appl
Pays: Germany
ID NLM: 101298608

Informations de publication

Date de publication:
07 2019
Historique:
received: 03 06 2018
revised: 04 11 2018
pubmed: 6 12 2018
medline: 25 1 2020
entrez: 6 12 2018
Statut: ppublish

Résumé

Damage to the uterosacral ligaments is an important contributor to uterine and vaginal prolapse. The aim of this study is to identify differentially expressed proteins (DEPs) in the uterosacral ligaments of women with and without pelvic organ prolapse (POP) and analyze their relationships to cellular mechanisms involved in the pathogenesis of POP. Uterosacral ligament connective tissue from four patients with POP and four control women undergo iTRAQ analysis followed by ingenuity pathway analysis (IPA) of DEPs. DEPs are validated using Western blot analysis. A total of 1789 unique protein sequences are identified in the uterosacral ligament connective tissues. The expression levels of 88 proteins are significantly different between prolapse and control groups (≥1.2-fold, p < 0.05). IPA demonstrates the association of 14 DEPs with "Connective Tissue Function." Among them, fibromodulin, collagen alpha-1 (XIV) chain, calponin-1, tenascin, and galectin-1 appear most likely to play a role in the etiology of POP. At least six proteins not previously associated with the pathogenesis of POP with biologic functions that suggest a plausible relationship to the disorder are identified. These results may be helpful for furthering the understanding of the pathophysiological mechanisms of POP.

Identifiants

pubmed: 30516354
doi: 10.1002/prca.201800086
doi:

Substances chimiques

Proteome 0

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1800086

Informations de copyright

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Auteurs

Xiang-Juan Li (XJ)

Key Laboratory of Reproductive Genetics, Ministry of Education, Zhejiang University, Hangzhou, 310058, China.
Hangzhou Women's Hospital, Hangzhou, 310008, China.

Hai-Tao Pan (HT)

Shaoxing Women and Children's Hospital, Shaoxing, 312000, China.

Juan-Juan Chen (JJ)

Hangzhou Women's Hospital, Hangzhou, 310008, China.

Yi-Bin Fu (YB)

Shaoxing Women and Children's Hospital, Shaoxing, 312000, China.

Min Fang (M)

Shaoxing Women and Children's Hospital, Shaoxing, 312000, China.

Guo-Hua He (GH)

Shaoxing Women and Children's Hospital, Shaoxing, 312000, China.

Tao Zhang (T)

Shaoxing Women and Children's Hospital, Shaoxing, 312000, China.

Hai-Gang Ding (HG)

Shaoxing Women and Children's Hospital, Shaoxing, 312000, China.

Bin Yu (B)

Shaoxing Women and Children's Hospital, Shaoxing, 312000, China.

Yi Cheng (Y)

Key Laboratory of Reproductive Genetics, Ministry of Education, Zhejiang University, Hangzhou, 310058, China.
Department of Pathology and Pathophysiology, School of Medicine, Zhejiang University, Hangzhou, 310058, China.

Ya-Jing Tan (YJ)

International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200240, China.

Fa-Lin Zhao (FL)

Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.

Abraham N Morse (AN)

Guangzhou Women and Children's Medical Center, Guangzhou, 510623, China.

He-Feng Huang (HF)

Key Laboratory of Reproductive Genetics, Ministry of Education, Zhejiang University, Hangzhou, 310058, China.
International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200240, China.

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Classifications MeSH