Title of article
A break-apart fluorescence in situ hybridization assay for detecting RET translocations in papillary thyroid carcinoma
Author/Authors
Chen، نويسنده , , Frank and Clark، نويسنده , , Douglas P. and Hawkins، نويسنده , , Anita L. and Morsberger، نويسنده , , Laura A. and Griffin، نويسنده , , Constance A.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
7
From page
128
To page
134
Abstract
At least 15 different translocations have been described activating RET in papillary thyroid carcinomas. A break-apart fluorescence in situ hybridization (FISH) assay should detect many translocations involving the RET gene without requiring knowledge of the partner gene. G-banding and spectral karyotyping was performed to further characterize the papillary carcinoma cell line TPC-1. BAC clones flanking the 5′ and 3′ regions of RET were labeled with SpectrumRed and biotin detected with avidin-AMCA (blue). In addition to the previously described chromosomal t(1;10;21), TPC-1 was found to have del(7)(q22q31) and der(8)t(8;8)(p21;q11.2). With the BAC probes, TPC-1 interphase nuclei showed the expected signal pattern of one paired red–blue signal as well as separated red and blue signals from the rearranged RET gene in 93% of cells. Interphase nuclei from normal human lymphocytes showed two paired red–blue signals in 97% of cells. TPC-1 cells were found to have the previously described chromosomal rearrangement that involves chromosome 10, with few other cytogenetically detectable genomic alterations. RET rearrangement can be detected by a break-apart BAC FISH probe set in the interphase nuclei of TPC-1 cells. This assay can potentially detect clinically relevant translocations involving RET.
Journal title
Cancer Genetics and Cytogenetics
Serial Year
2007
Journal title
Cancer Genetics and Cytogenetics
Record number
1828731
Link To Document