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 |
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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. |
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ISSN: | 0893-3952 1530-0285 |
DOI: | 10.1038/s41379-018-0098-3 |