scholarly journals Osteopontin as a Potential Diagnostic Biomarker for Ovarian Cancer

JAMA ◽  
2002 ◽  
Vol 287 (13) ◽  
pp. 1671 ◽  
Author(s):  
Jae-Hoon Kim
2019 ◽  
Vol Volume 12 ◽  
pp. 9715-9723 ◽  
Author(s):  
Yingchao Hu ◽  
Yapei Zhu ◽  
Wen Zhang ◽  
Jinghe Lang ◽  
Li Ning

2014 ◽  
Vol 23 (4) ◽  
pp. 611-621 ◽  
Author(s):  
Kyoungmi Kim ◽  
L. Renee Ruhaak ◽  
Uyen Thao Nguyen ◽  
Sandra L. Taylor ◽  
Lauren Dimapasoc ◽  
...  

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e10817
Author(s):  
Huiting Xiao ◽  
Kun Wang ◽  
Dan Li ◽  
Ke Wang ◽  
Min Yu

Background Malignant ovarian cancer is associated with the highest mortality of all gynecological tumors. Designing therapeutic targets that are specific to OC tissue is important for optimizing OC therapies. This study aims to identify different expression patterns of genes related to FGFR1 and the usefulness of FGFR1 as diagnostic biomarker for OC. Methods We collected data from The Cancer Genome Atlas (TCGA) and the Gene Expression Omnibus (GEO) databases. In the TCGA cohort we analyzed clinical information according to patient characteristics, including age, stage, grade, longest dimension of the tumor and the presence of a residual tumor. GEO data served as a validation set. We obtained data on differentially expressed genes (DEGs) from the two microarray datasets. We then used gene set enrichment analysis (GSEA) to analyze the DEG data in order to identify enriched pathways related to FGFR1. Results Differential expression analysis revealed that FGFR1 was significantly downregulated in OC specimens. 303 patients were included in the TCGA cohort. The GEO dataset confirmed these findings using information on 75 Asian patients. The GSE105437 and GSE12470 database highlighted the significant diagnostic value of FGFR1 in identifying OC (AUC = 1, p = 0.0009 and AUC = 0.8256, p = 0.0015 respectively). Conclusions Our study examined existing TCGA and GEO datasets for novel factors associated with OC and identified FGFR1 as a potential diagnostic factor. Further investigation is warranted to characterize the role played by FGFR1 in OC.


2021 ◽  
Vol 11 (12) ◽  
pp. 1335
Author(s):  
Hina Amer ◽  
Apriliana E. R. Kartikasari ◽  
Magdalena Plebanski

Ovarian cancer (OC) is one of the most lethal cancers, largely due to a late diagnosis. This study aimed to provide a comprehensive meta-analysis on the diagnostic performance of IL6 in the blood and ascites separately for advanced and early-stage OC. We included 37 studies with 6948 participants detecting serum or plasma IL6. The plasma/serum IL6 mean level in the late-stage OC was 23.88 pg/mL (95% CI: 13.84–41.23), and the early-stage OC was 16.67 pg/mL (95% CI: 510.06–27.61), significantly higher than the healthy controls at 3.96 pg/mL (95% CI: 2.02–7.73), but not significantly higher than those found in the controls with benign growths in the ovary, which was 9.63 pg/mL (95% CI: 4.16–22.26). To evaluate IL6 in ascites as a diagnostic marker, we included 26 studies with 1590 participants. The mean level of ascitic IL6 in the late-stage OC was 3676.93 pg/mL (95% CI: 1891.7–7146.7), and the early-stage OC was 1519.21 pg/mL (95% CI: 604.6–3817.7), significantly higher than the benign controls at 247.33 pg/mL (95% CI: 96.2–636.0). There was no significant correlation between the levels of circulating and ascitic IL6. When pooling all OC stages for analysis, we found that serum/plasma IL6 provided 76.7% sensitivity (95% CI: 0.71–0.92) and 72% specificity (95% CI: 0.64–0.79). Ascitic IL6 provided higher sensitivity at 84% (95% CI: 0.710–0.919) and specificity at 74% (95% CI: 0.646–0.826). This study highlights the utility of ascitic IL6 for early detection of OC.


2021 ◽  
Author(s):  
Louise Faaborg ◽  
Anders Jakobsen ◽  
Marianne Waldstrøm ◽  
Christina B Petersen ◽  
Rikke F Andersen ◽  
...  

Aim: In ovarian cancer, methylated HOXA9 (meth-HOXA9) has been proposed as a relevant biomarker, however, its role in the carcinogenic development remains unknown. This study aimed at evaluating meth-HOXA9 as a diagnostic biomarker in ovarian cancer. Materials & methods: The meth-HOXA9 status was examined in 138 tissue specimens encompassing normal ovaries, benign- and borderline tumors, and ovarian cancer using droplet digital PCR. Results: Meth-HOXA9 was detected in 93% (82/88) and 88% (14/16) of ovarian cancer and borderline tumors, respectively. In patients with benign ovarian tumors meth-HOXA9 was detected in 17% (3/18). Using receiver operating characteristic (ROC) analysis meth-HOXA9 had a diagnostic accuracy of 98%. Conclusion: Meth-HOXA9 is highly cancer specific and could serve as a general diagnostic marker of ovarian malignancy.


2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Bipradeb Singha ◽  
Sandra L. Harper ◽  
Aaron R. Goldman ◽  
Benjamin G. Bitler ◽  
Katherine M. Aird ◽  
...  

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