| Literature DB >> 24824029 |
Rory L Cochran1, Karen Cravero1, David Chu1, Bracha Erlanger1, Patricia Valda Toro1, Julia A Beaver1, Daniel J Zabransky1, Hong Yuen Wong1, Justin Cidado1, Sarah Croessmann1, Heather Parsons1, Minsoo Kim1, Sarah J Wheelan1, Pedram Argani1, Ben Ho Park1.
Abstract
Loss-of-heterozygosity (LOH) analysis of archival tumor tissue can aid in determining the clinical significance of BRCA variants. Here we describe an approach for assessing LOH in formalin-fixed, paraffin-embedded (FFPE) tissues using variant-specific probes and droplet digital polymerase chain reaction (ddPCR). We evaluated LOH in 2 related breast cancer patients harboring a rare missense BRCA2 variant of unknown clinical significance (c.6966G>T; M2322I). Conventional PCR followed by Sanger sequencing suggested a change in allelic abundance in the FFPE specimens. However, we found no evidence of LOH as determined by the allelic ratio (wild type-variant) for BRCA2 in both patients' archival tumor specimens and adjacent normal control tissues using ddPCR. In summary, these experiments demonstrate the utility of ddPCR to quickly and accurately assess LOH in archival FFPE tumor tissue.Entities:
Keywords: BRCA2; Droplet digital PCR; Familial breast cancer; LOH; VUS
Mesh:
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Year: 2014 PMID: 24824029 PMCID: PMC4065621 DOI: 10.1016/j.humpath.2014.03.013
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466