'Chromosomal Rainbows' Detect Oncogenic Rearrangements of Signaling Molecules in Thyroid Tumors
Benjamin O'Brien1, Gregg H Jossart, Yuko Ito
1Life Sciences Division, E.O. Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
Abstract:
Altered signal transduction can be considered a hallmark of many solid tumors. In thyroid cancers the receptor tyrosine kinase (rtk) genes NTRK1 (Online Mendelian Inheritance in Man = OMIM *191315, also known as 'TRKA'), RET ('Rearranged during Transfection protooncogene', OMIM *164761) and MET (OMIM *164860) have been reported as activated, rearranged or overexpressed. In many cases, a combination of cytogenetic and molecular techniques allows elucidation of cellular changes that initiate tumor development and progression. While the mechanisms leading to overexpression of the rtk MET gene remain largely unknown, a variety of chromosomal rearrangements of the RET or NTKR1 gene could be demonstrated in thyroid cancer. Abnormal expressions in these tumors seem to follow a similar pattern: the rearrangement translocates the 3'- end of the rtk gene including the entire catalytic domain to an expressed gene leading to a chimeric RNA and protein with kinase activity. Our research was prompted by an increasing number of reports describing translocations involving ret and previously unknown translocation partners.We developed a high resolution technique based on fluorescence in situ hybridization (FISH) to allow rapid screening for cytogenetic rearrangements which complements conventional chromosome banding analysis. Our technique applies simultaneous hybridization of numerous probes labeled with different reporter molecules which are distributed along the target chromosome allowing the detection of cytogenetic changes at near megabasepair (Mbp) resolution. Here, we report our results using a probe set specific for human chromosome 10, which is altered in a significant portion of human thyroid cancers (TC's). While rendering accurate information about the cytogenetic location of rearranged elements, our multi-locus, multi-color analysis was developed primarily to overcome limitations of whole chromosome painting (WCP) and chromosome banding techniques for fine mapping of breakpoints in papillary thyroid cancer (PTC).
Insights
Altered receptor tyrosine kinase (RTK) genes like RET and NTRK1 are key in thyroid cancer. New FISH techniques precisely map chromosomal rearrangements in these cancers, aiding diagnosis.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Altered signal transduction is a hallmark of solid tumors, including thyroid cancer.
- Receptor tyrosine kinase (RTK) genes NTRK1, RET, and MET are frequently altered in thyroid cancers through activation, rearrangement, or overexpression.
- Chromosomal rearrangements involving RET and NTRK1 in thyroid cancer often lead to chimeric proteins with aberrant kinase activity.
Purpose of the Study:
- To develop and apply a high-resolution fluorescence in situ hybridization (FISH) technique for rapid screening of cytogenetic rearrangements in thyroid cancer.
- To complement conventional chromosome banding analysis for precise mapping of translocation breakpoints.
- To investigate alterations in human chromosome 10, which is frequently affected in thyroid cancers.
Main Methods:
- Development of a high-resolution FISH technique utilizing simultaneous hybridization of multiple probes with different reporter molecules.
- Application of a probe set specific for human chromosome 10.
- Multi-locus, multi-color FISH analysis for fine mapping of breakpoints.
Main Results:
- The developed FISH technique allows for near megabasepair (Mbp) resolution detection of cytogenetic changes.
- The study reports results from applying the FISH technique to human chromosome 10 in thyroid cancer samples.
- The multi-locus, multi-color analysis effectively overcomes limitations of whole chromosome painting and chromosome banding for breakpoint mapping in papillary thyroid cancer.
Conclusions:
- The high-resolution FISH technique is a valuable tool for rapid screening and precise mapping of cytogenetic rearrangements in thyroid cancer.
- This method aids in understanding the mechanisms of tumor development and progression driven by RTK gene alterations.
- The findings contribute to improved diagnostic and prognostic capabilities for thyroid cancer, particularly papillary thyroid cancer.


