| Literature DB >> 31211411 |
Sapir Margalit1, Sigal Avraham1, Tamar Shahal1, Yael Michaeli1, Noa Gilat1, Prerna Magod2, Michal Caspi3, Shelly Loewenstein4,5, Guy Lahat4,5, Dinorah Friedmann-Morvinski2, Revital Kariv3,6, Rina Rosin-Arbesfeld3, Shahar Zirkin1, Yuval Ebenstein1.
Abstract
Epigenetic transformations may provide early indicators for cancer and other disease. Specifically, the amount of genomic 5-hydroxymethylcytosine (5-hmC) was shown to be globally reduced in a wide range of cancers. The integration of this global biomarker into diagnostic workflows is hampered by the limitations of current 5-hmC quantification methods. Here we present and validate a fluorescence-based platform for high-throughput and cost-effective quantification of global genomic 5-hmC levels. We utilized the assay to characterize cancerous tissues based on their 5-hmC content, and observed a pronounced reduction in 5-hmC level in various cancer types. We present data for glioblastoma, colorectal cancer, multiple myeloma, chronic lymphocytic leukemia and pancreatic cancer, compared to corresponding controls. Potentially, the technique could also be used to follow response to treatment for personalized treatment selection. We present initial proof-of-concept data for treatment of familial adenomatous polyposis.Entities:
Keywords: 5-hmC; 5-hydroxymethylcytosine; cancer; epigenetic biomarker; epigenetics; fluorescence
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Year: 2019 PMID: 31211411 DOI: 10.1002/ijc.32519
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396