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1.
Tumour Biol ; 36(3): 1711-20, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25427637

ABSTRACT

The current methods available for screening and detecting cervical squamous cell carcinoma (CSCC) have insufficient sensitivity and specificity. As a result, many patients suffered from erroneous and missed diagnosis. Because CSCC is usually asymptomatic at potentially curative stages, identification of biomarkers is an urgent need for the early detection of CSCC. Comparative proteomics based on two-dimensional differential in-gel electrophoresis (2D-DIGE) was employed to quantitatively analyze plasma proteins of healthy Uyghur women and with early stage cervical carcinoma. The 2D-DIGE image were analyzed statistically using DeCyder™ 2D software. The statistical analysis of proteomic data revealed that 43 protein spots showed significantly different expression (ratio > 1.5, P < 0.01). A further identification of these protein spots by MALDI-TOF-MS found out 16 different proteins. Bioinformatic analysis within the framework of Ingenuity Pathway Analysis (IPA(@)) showed that 10 plasma proteins as candidate biomarker were screened, mainly including lipid metabolism-related proteins (APOA4, APOA1, APOE), complement (EPPK1, CFHR1), metabolic enzymes (CP, F2, MASP2), glycoprotein (CLU), and immune function-related proteins (IGK@). Networks involved in lipid metabolism, molecular transport, and small molecule biochemistry were dysfunctional in CSCC. Acute phase response signaling and JAK/Stat signaling and IL-4 signaling, etc., were identified as the canonical pathways that are overrepresented in CSCC. Furthermore, the expression of three proteins (APOA1, APOE, CLU) were validated using ELISA in plasma of patients with different stage cervical lesion. With the combined proteomic and bioinformatic approach, this study was successful in identifying biomarker signatures for cervical cancer and might provide new insights into the mechanism of CSCC progression, potentially leading to the design of novel diagnostic and therapeutic strategies.


Subject(s)
Biomarkers, Tumor/metabolism , Proteome/metabolism , Uterine Cervical Neoplasms/diagnosis , Uterine Cervical Neoplasms/metabolism , Adult , Aged , Blood Proteins/metabolism , Electrophoresis, Gel, Two-Dimensional/methods , Female , Glycoproteins/metabolism , Humans , Interleukin-4/metabolism , Middle Aged , Neoplasm Proteins/metabolism , Proteomics/methods , Signal Transduction , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods , Two-Dimensional Difference Gel Electrophoresis/methods
2.
Biomarkers ; 17(4): 352-61, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22458349

ABSTRACT

OBJECTIVE: To identify plasma protein biomarkers of cervical high-grade squamous intraepithelial lesion (HSIL) of Uyghur women by proteomics approach. METHODS: Plasma protein samples of Uyghur women with HSIL and chronic cervicitis were analyzed with 2D HPLC followed by detection of target proteins with Linear Trap Quadrupole Mass Spectrometer (LTQ MS/MS). RESULTS: We detected three upregulated and one downregulated protein peaks representing protein constituents distinguishing HSIL from controls by 2D HPLC, identified 31 target proteins by LTQ MS/MS. Further confirmed analysis with online software IPA® 8.7 and ELISA assay showed APOA1 and mTOR as potential biomarkers. CONCLUSIONS: A distinct plasma proteomic profile may be associated with HSIL of Uyghur women.


Subject(s)
Apolipoprotein A-I/blood , Biomarkers, Tumor/blood , TOR Serine-Threonine Kinases/blood , Uterine Cervical Dysplasia/blood , Uterine Cervical Neoplasms/blood , Adult , Apolipoprotein A-I/isolation & purification , Asian People , Biomarkers, Tumor/isolation & purification , Blood Proteins/isolation & purification , Blood Proteins/metabolism , Brachial Plexus Neuritis , Chromatography, Reverse-Phase , Early Detection of Cancer , Female , Humans , Intercellular Signaling Peptides and Proteins/blood , Intercellular Signaling Peptides and Proteins/isolation & purification , Middle Aged , Placental Lactogen , Proteomics , TOR Serine-Threonine Kinases/isolation & purification , Tandem Mass Spectrometry , Uterine Cervical Neoplasms/diagnosis , Uterine Cervicitis/blood , Uterine Cervical Dysplasia/diagnosis
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