Determination of biological behavior of solitary fibrous tumors: correlation of expression of Ki-67, TPX2 and TERT mRNA subunit level and NAB2-STAT6 fusion compared to morphological aspects of SFTs.
Biomarkers, Tumor
/ genetics
Cell Cycle Proteins
Humans
Immunohistochemistry
Ki-67 Antigen
/ genetics
Microtubule-Associated Proteins
Neoplasm Recurrence, Local
RNA, Messenger
/ genetics
Repressor Proteins
Retrospective Studies
STAT6 Transcription Factor
/ genetics
Solitary Fibrous Tumors
/ genetics
Telomerase
/ genetics
Journal
Neoplasma
ISSN: 0028-2685
Titre abrégé: Neoplasma
Pays: Slovakia
ID NLM: 0377266
Informations de publication
Date de publication:
Jan 2022
Jan 2022
Historique:
received:
11
05
2021
accepted:
02
08
2021
pubmed:
25
11
2021
medline:
15
2
2022
entrez:
24
11
2021
Statut:
ppublish
Résumé
We present a retrospective study of 65 cases of solitary fibrous tumors (SFTs) of several localizations including the most common site of origin in the pleura and lungs. SFTs are mesenchymal fibroblastic tumors with an unpredictable biological potential ranging from benign to malignant. We investigated morphologic characteristics, proliferation activity evaluated by immunohistochemical expression of Ki-67 antigen, and the existence of NAB2-STAT6 fusion gene together with Ki-67, TPX2, and TERT mRNA expression levels. The aim was to define relationships between proliferation activity and biological potential and progression of the disease. We measured Ki-67, TPX2, and TERT mRNA levels using quantitative real-time reverse transcription PCR (RQ-RT-PCR). We observed a significant association between increased Ki-67 and TERT mRNA levels and the SFTs with malignant potential. Also, we investigated the effect of TERT promoter mutation on telomerase activation and patient outcome in our SFT cohort. We verified that TERT promoter mutation was frequent (36.6%) and present in a majority of malignant SFTs and SFTs with uncertain biological behavior. TERT promoter mutation alone predicted the disease recurrence.
Identifiants
pubmed: 34818026
doi: 10.4149/neo_2021_210511N642
pii: 210511N642
doi:
pii:
Substances chimiques
Biomarkers, Tumor
0
Cell Cycle Proteins
0
Ki-67 Antigen
0
Microtubule-Associated Proteins
0
NAB2 protein, human
0
RNA, Messenger
0
Repressor Proteins
0
STAT6 Transcription Factor
0
STAT6 protein, human
0
TPX2 protein, human
0
TERT protein, human
EC 2.7.7.49
Telomerase
EC 2.7.7.49
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM