| Literature DB >> 30981729 |
Ankit Sinha1, Ali Hussain1, Vladimir Ignatchenko2, Alexandr Ignatchenko2, Kwan Ho Tang3, Victor W H Ho2, Benjamin G Neel4, Blaise Clarke5, Marcus Q Bernardini6, Laurie Ailles7, Thomas Kislinger8.
Abstract
High-grade serous ovarian carcinoma (HGSC) is the most common and lethal subtype of gynecologic malignancy in women. The current standard of treatment combines cytoreductive surgery and chemotherapy. Despite the efficacy of initial treatment, most patients develop cancer recurrence, and 70% of patients die within 5 years of initial diagnosis. CA125 is the current FDA-approved biomarker used in the clinic to monitor response to treatment and recurrence, but its impact on patient survival is limited. New strategies for the discovery of HGSC biomarkers are urgently needed. Here, we describe a proteomics strategy to detect tumor-associated proteins in serum of HGSC patient-derived xenograft models. We demonstrate proof-of-concept applicability using two independent, longitudinal serum cohorts from HGSC patients.Entities:
Keywords: N-glycosylation; biomarker; ovarian cancer; patient-derived xenograft; serum proteomics; targeted proteomics
Mesh:
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Year: 2019 PMID: 30981729 DOI: 10.1016/j.cels.2019.03.011
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304