Document Detail


Comparative proteomic analysis between benign and malignant-transformed hydatidiform mole.
MedLine Citation:
PMID:  18773628     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: To explore the differential protein expression between benign/remitting and malignant-transformed hydatidiform mole. STUDY DESIGN: Proteomic analysis was carried out on 7 remitting (including 3 partial moles and 4 complete moles) and 11 malignant-transformed (including 4 partial moles and 7 complete moles) hydatidiform moles. The extracted protein was separated with 2-dimensional electrophoresis, and differentially expressed proteins were analyzed and identified by matrix-assisted desorption/ionization time-of-flight spectrometry (MALDI-TOF-MS). RESULTS: A total of 32 differentially expressed spots were selected. Of these, 17 spots were identified through database searching, mainly involving cytoskeletal protein, stress-associated proteins, apoptosis-associated protein, proteins involved in signal transduction, cell proliferation and differentiation, etc. Of these, 11 might be related to the malignant transformation of hydatidiform mole. CONCLUSION: Seventeen differentially expressed proteins were identified, of which 11 might be associated with malignant transformation of hydatidiform mole. This has laid a foundation for further screening of biomarkers that predict prognosis of hydatidiform mole.
Authors:
Li Ma; Yang Xiang; Jun Zhao; Fengzhi Feng; Xirun Wan
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Journal of reproductive medicine     Volume:  53     ISSN:  0024-7758     ISO Abbreviation:  J Reprod Med     Publication Date:  2008 Aug 
Date Detail:
Created Date:  2008-09-08     Completed Date:  2009-01-16     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0173343     Medline TA:  J Reprod Med     Country:  United States    
Other Details:
Languages:  eng     Pagination:  623-8     Citation Subset:  IM    
Affiliation:
Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing, People's Republic of China.
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MeSH Terms
Descriptor/Qualifier:
Adult
Cell Transformation, Neoplastic*
Cohort Studies
Disease Progression
Female
Humans
Hydatidiform Mole / metabolism*,  pathology
Middle Aged
Neoplasm Proteins / metabolism*
Pregnancy
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Tumor Markers, Biological / metabolism*
Up-Regulation
Uterine Neoplasms / metabolism*,  pathology
Young Adult
Chemical
Reg. No./Substance:
0/Neoplasm Proteins; 0/Tumor Markers, Biological

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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