| Literature DB >> 26921541 |
Maja H Oktay1, Esther Adler2, Laleh Hakima2, Eli Grunblatt3, Evan Pieri3, Andrew Seymour2, Samer Khader2, Antonio Cajigas2, Mark Suhrland2, Sumanta Goswami4.
Abstract
Detection of mutational alterations is important for guiding treatment decisions of lung non-small-cell carcinomas and thyroid nodules with atypical cytologic findings. Inoperable lung tumors requiring further testing for staging and thyroid lesions often are diagnosed using only cytology material. Molecular diagnostic tests of these samples typically are performed on cell blocks; however, insufficient cellularity of cell blocks is a limitation for test performance. In addition, some of the fixatives used while preparing cell blocks often introduces artifacts for mutation detection. Here, we applied qClamp xenonucleic technology and quantitative RT-PCR to cells microdissected directly from stained cytology smears to detect common alterations including mutations and translocations in non-small-cell carcinomas and thyroid lesions. By using this approach, we achieved a 1% molecular alteration detection rate from as few as 50 cells. Ultrasensitive methods of molecular alteration detection similar to the one described here will be increasingly important for the evaluation of molecular alterations in clinical scenarios when only tissue samples that are small are available.Entities:
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Year: 2016 PMID: 26921541 DOI: 10.1016/j.jmoldx.2016.01.007
Source DB: PubMed Journal: J Mol Diagn ISSN: 1525-1578 Impact factor: 5.568