期刊论文详细信息
BMC Cancer | |
LOH at 6q and 10q in fractionated circulating DNA of ovarian cancer patients is predictive for tumor cell spread and overall survival | |
Research Article | |
Sabine Kasimir-Bauer1  Jan Dominik Kuhlmann1  Pauline Wimberger1  Rainer Kimmig1  Micaela Poetsch2  Heidi Schwarzenbach3  | |
[1]Department of Gynecology and Obstetrics, University Hospital of Essen, Hufelandstrasse 55, D-45122, Essen, Germany | |
[2]Institute of Legal Medicine, University Hospital of Essen, Essen, Germany | |
[3]Institute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany | |
关键词: Circulating DNA; Loss of heterozygosity; Disseminated tumor cells; DNA-fractionation; Tumor suppressor genes; | |
DOI : 10.1186/1471-2407-12-325 | |
received in 2012-03-30, accepted in 2012-07-18, 发布年份 2012 | |
来源: Springer | |
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【 摘 要 】
BackgroundWe recently showed that LOH proximal to M6P/IGF2R locus (D6S1581) in primary ovarian tumors is predictive for the presence of disseminated tumor cells (DTC) in the bone marrow (BM). For therapy-monitoring, it would be highly desirable to establish a blood-based biomarker. Therefore, we quantified circulating DNA (cirDNA) in sera of 63 ovarian cancer patients before surgery and after chemotherapy, measured incidence of LOH at four cancer-relevant chromosomal loci, correlated LOH with tumor cell spread to the BM and evaluated prognostic significance of LOH.MethodscirDNA was fractionated into high- and low molecular-weight fraction (HMWF, LMWF) for LOH-profiling, utilizing PCR-based fluorescence microsatellite analysis. BM aspirates were analyzed for DTC by immunocytochemistry using the pan-cytokeratin antibody A45-B/B3.ResultscirDNA levels in the HMWF before surgery were predictive for residual tumor load (p = 0.017). After chemotherapy, we observed a significant decline of cirDNA in the LMWF (p = 0.0001) but not in the HMWF. LOH was prevalently detected in the LMWF with an overall frequency of 67%, only moderately ablating after chemotherapy (45%). Before surgery, LOH in the LMWF at marker D10S1765 and D13S218 significantly correlated with tumor grading and FIGO stage (p = 0.033, p = 0.004, respectively). In both combined fractions, LOH at D6S1581 additionally associated with overall survival (OS) (p = 0.030). Moreover, solely LOH at D10S1765 in LMWF after therapy correlated with DTC in BM after therapy (p = 0.017).ConclusionWe demonstrate the applicability and necessity of DNA-fractionation prior to analyzing circulating LOH and identify LOH at D10S1765 and D6S1581 as novel blood-based biomarkers for ovarian cancer, being relevant for therapy-monitoring.【 授权许可】
CC BY
© Kuhlmann et al.; licensee BioMed Central Ltd. 2012
【 预 览 】
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