In Japanese patients with papillary thyroid carcinoma, TERT promoter mutation is associated with poor prognosis, in contrast to BRAFV600E mutation
The prognostic value of BRAF V600E and TERT promoter mutation in papillary thyroid carcinoma (PTC) is controversial. We examined alterations in BRAF V600E and TERT promoter by PCR-direct sequencing in PTC of 144 Japanese patients. Alternative lengthening of telomeres was examined as another mechanis...
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Veröffentlicht in: | Virchows Archiv : an international journal of pathology 2016, Vol.469 (6), p.687-696 |
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Sprache: | eng |
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Zusammenfassung: | The prognostic value of
BRAF
V600E
and
TERT
promoter mutation in papillary thyroid carcinoma (PTC) is controversial. We examined alterations in
BRAF
V600E
and
TERT
promoter by PCR-direct sequencing in PTC of 144 Japanese patients. Alternative lengthening of telomeres was examined as another mechanism of telomere maintenance by immunohistochemical staining for ATRX and DAXX. Of the clinicopathological characteristics, regional lymph node metastasis, extra-thyroid extension, multifocality/intrathyroidal spread, and advanced stage (III/V) were associated with shorter disease-free survival rate (DFSR).
TERT
promoter mutation was found in eight patients (6 %), and this was significantly associated with total thyroidectomy, multifocality/intrathyroidal spread, lymph node metastasis and advanced stage. The
BRAF
V600E
mutation was found in 53 patients (38.2 %) but was not associated with any clinicopathological factors.
TERT
mutations were not correlated with
BRAF
V600E
mutation status.
TERT
mutation-positive tumors (
TERT
+) showed lower DFSR than
BRAF
V600E
-mutation-positive tumors (
BRAF
V600E
+
), and
TERT
+/
BRAF
V600E
+ tumors showed lower DFSR than
BRAF
V600E
+ tumors. No cases showed loss of ATRX/DAXX expression by immunohistochemistry.
TERT
promoter mutations showed a lower prevalence in our series and appeared to be associated with aggressive behavior. In PTCs, telomerase activation by
TERT
promoter mutation might be more important than alternative lengthening of telomeres. |
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ISSN: | 0945-6317 1432-2307 |
DOI: | 10.1007/s00428-016-2027-5 |