Telomerase expression in clinically non-functioning pituitary adenomas

被引:2
作者
Ogino, Liana Lumi [1 ]
Lamback, Elisa Baranski [2 ,3 ]
Guterres, Alexandro [1 ]
de Azeredo Lima, Carlos Henrique [1 ]
Henriques, Daniel Gomes [2 ,3 ]
Barbosa, Monique Alvares [4 ]
Silva, Debora Aparecida [1 ]
da Silva Camacho, Aline Helen [1 ,5 ]
Chimelli, Leila [1 ]
Kasuki, Leandro [2 ,3 ,6 ,7 ]
Gadelha, Monica R. [1 ,2 ,3 ,6 ]
机构
[1] Inst Estadual Cerebro Paulo Niemeyer, Neuropathol & Mol Genet Lab, Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Med Sch, Neuroendocrinol Res Ctr, Endocrinol Div, Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Hosp Univ Clementino Fraga Filho, Rio De Janeiro, Brazil
[4] Inst Estadual Cerebro Paulo Niemeyer, Radiol Div, Rio De Janeiro, Brazil
[5] Inst Nacl Canc, Pathol Div, Rio De Janeiro, Brazil
[6] Inst Estadual Cerebro Paulo Niemeyer, Neuroendocrinol Div, Rio De Janeiro, Brazil
[7] Hosp Fed Bonsucesso, Endocrinol Div, Rio De Janeiro, Brazil
关键词
Non-functioning pituitary adenomas; Telomerase; Tumorigenesis; Pituitary tumor; 2ND BRAIN-TUMOR; CONSERVATIVE SURGERY; RADIATION-THERAPY; REVERSE-TRANSCRIPTASE; RADIOTHERAPY; CLASSIFICATION; CANCER; LENGTH; HTERT; PROLIFERATION;
D O I
10.1007/s12020-020-02524-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose Non-functioning pituitary adenomas (NFPA) are benign tumors, however, some are agressive. We aimed to assess if human telomerase reverse transcriptase (hTERT) is present in NFPA and if it can be used as a marker of aggressiveness and proliferation. Methods Consecutive patients operated for NFPA whose fresh frozen tumors were available were included. We analyzed tumor's aggressiveness (based on radiological progression) and proliferation (based on Ki-67), as well as hTERT mRNA by quantitative real-time polymerase chain reaction (RT-qPCR). Results We included 109 samples from 86 patients followed for a median period of 60 months (5-120 months). Aggressive tumors were present in 66% cases and proliferative tumors in 47.7%. Seven (6.4%) samples expressed hTERT: 3 (42.8%) had aggressive and proliferative tumors, 2 (28.6%) only exhibited aggressiveness and the remaining 2 (28.6%) only proliferation. From the aggressive and proliferative tumors, 14% and 16%, respectively, expressed hTERT. From the non-aggressive and non-proliferative tumors, 9% and 6%, respectively, expressed hTERT. Conclusion hTERT expression is present in a minority of NFPA and does not seem to be related to aggressiveness or proliferation in NFPA.
引用
收藏
页码:208 / 215
页数:8
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