Article
Identification of potential serum markers for endometrial cancer using protein expression profiling.
Department of Obstetrics and Gynecology, National Defense Medical College, Tokorozawa, Saitama, 359-8513, Japan.
Journal of Cancer Research and Clinical Oncology (impact factor:
2.56).
09/2009;
136(3):475-81.
DOI:10.1007/s00432-009-0680-7
Source: PubMed
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Citations (0)
- Cited In (2)
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Article: Serum Biomarkers for Early Detection of Gynecologic Cancers
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ABSTRACT: Ovarian, endometrial, and cervical cancers are three of the most common malignancies of the female reproductive organs. CA 125, historically the most reliable serum marker for ovarian cancer, is elevated in 50% of early-stage ovarian tumors. For endometrial cancers, there are no established serum markers. SCC, which is the best studied serum marker for squamous cell carcinomas, has been unreliable; SCC is elevated in cervical squamous cell carcinomas ranging from 28–85% of the time. Recent proteomics-based analyses show great promise for the discovery of new and more useful biomarkers. In this review, we will discuss the currently utilized serum tumor markers for gynecologic cancers and the novel biomarkers that are now under investigation.Cancers. 01/2010; -
Article: Altered protein expression in serum from endometrial hyperplasia and carcinoma patients.
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ABSTRACT: Endometrial carcinoma is one of the most common gynecological malignancies in women. The diagnosis of the disease at early or premalignant stages is crucial for the patient's prognosis. To date, diagnosis and follow-up of endometrial carcinoma and hyperplasia require invasive procedures. Therefore, there is considerable demand for the identification of biomarkers to allow non-invasive detection of these conditions. In this study, we performed a quantitative proteomics analysis on serum samples from simple endometrial hyperplasia, complex endometrial hyperplasia, atypical endometrial hyperplasia, and endometrial carcinoma patients, as well as healthy women. Serum samples were first depleted of high-abundance proteins, labeled with isobaric tags (iTRAQ), and then analyzed via two-dimensional liquid chromatography and tandem mass spectrometry. Protein identification and quantitation information were acquired by comparing the mass spectrometry data against the International Protein Index Database using ProteinPilot software. Bioinformatics annotation of identified proteins was performed by searching against the PANTHER database. In total, 74 proteins were identified and quantified in serum samples from endometrial lesion patients and healthy women. Using a 1.6-fold change as the benchmark, 12 proteins showed significantly altered expression levels in at least one disease group compared with healthy women. Among them, 7 proteins were found, for the first time, to be differentially expressed in atypical endometrial hyperplasia. These proteins are orosomucoid 1, haptoglobin, SERPINC 1, alpha-1-antichymotrypsin, apolipoprotein A-IV, inter-alpha-trypsin inhibitor heavy chain H4, and histidine-rich glycoprotein. The differentially expressed proteins we discovered in this study may serve as biomarkers in the diagnosis and follow-up of endometrial hyperplasia and endometrial carcinoma.Journal of Hematology & Oncology 01/2011; 4:15. · 3.99 Impact Factor
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Keywords
40 controls
40 EC patients
65 EC patients
apolipoprotein A1
apolipoprotein C1
biomarker candidates
blind test
dual-biomarker analysis
EC patients
endometrial cancer
ionization-time-of-flight mass spectrometry
modified form
new biomarkers
protein profiles
Screening
screening method
SELDI-TOF MS
serum biomarkers
specificity
surface-enhanced laser desorption