hTERT promoter mutations in chondrosarcomas associate with progression and disease-related mortality

Chondrosarcomas are malignant skeletal tumors with chondroid differentiation. Prognosis is largely dependent on histological grading, which suffer from significant interobserver variability. Telomerase activity and abundant telomerase reverse transcriptase ( hTERT ) expression has previously been as...

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Veröffentlicht in:Modern pathology 2018-12, Vol.31 (12), p.1834-1841
Hauptverfasser: Lin, Yingbo, Seger, Nelly, Chen, Yi, Hesla, Asle C., Wejde, Johan, Ghaderi, Mehran, Tsagkozis, Panagiotis, Larsson, Olle, Haglund, Felix
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Sprache:eng
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Zusammenfassung:Chondrosarcomas are malignant skeletal tumors with chondroid differentiation. Prognosis is largely dependent on histological grading, which suffer from significant interobserver variability. Telomerase activity and abundant telomerase reverse transcriptase ( hTERT ) expression has previously been associated with chondrosarcoma grade and metastasis. We therefore analyzed the hTERT promoter in clinicopathologically well-characterized chondrosarcomas (grade 1–3) from 87 patients. Using Sanger sequencing we identified an activating −124 C > T mutation in 23 cases (26%). Promoter mutations were significantly associated with increased histological grade (8% of grade 1, 32% of grade 2 and 46% of grade 3, P  = 0.002), suggesting a role in tumor progression. In four chondrosarcomas where the histopathological grade was heterogenous, the hTERT mutation was only identified in the higher-grade areas. Additionally, hTERT promoter mutations were significantly associated with worse metastasis-free survival ( P  = 0.018), chondrosarcoma-specific survival ( P  = 0.022) and older patient age ( P  = 0.003). These data suggest that hTERT promoter mutations are common in high grade conventional chondrosarcomas. Granted that additional studies can confirm these findings; hTERT promoter analysis could potentially serve as an adjuvant prognostic marker in routine chondrosarcoma grading. This study reinforces the rationale of telomerase targeted therapy in a subset of chondrosarcomas.
ISSN:0893-3952
1530-0285
DOI:10.1038/s41379-018-0098-3