B. Macnamara et al., Telomerase activity in relation to pro- and anti-apoptotic protein expression in high grade non-Hodgkin's lymphomas, HAEMATOLOG, 86(4), 2001, pp. 386-393
Background and Objectives. Telomerase activity (TA) is determined by the ca
talytic unit telomerase reverse transcriptase (hTERT). In vitro studies sho
w that hTERT is downregulated by wild type p53 and TA is upregulated by BCL
-2 expression. The aim of this study was to investigate the relationship of
TA and mRNA expression of hTERT, telomerase RNA (hTER) and Tankyrase in 31
samples from patients with high-grade non-Hodgkin's lymphoma (HG-NHL). The
results were then related to apoptosis and proliferation and the expressio
n of p53 and BCL-2 family member proteins.
Design and Methods, The telomeric repeat amplification protocol (TRAP) assa
y and reverse transcription-polymerase chain reaction (RT-PCR) were used to
quantify TA, and hTERT, hTER and Tankyrase mRPIA expression. Proliferation
(Ki67), p53, BCL-2, MCL-1, BAX and BAK protein expression were evaluated b
y immunohistochemistry. Apoptosis was evaluated by TUNEL staining.
Results, TA was detected in 93% of HG-NHL and tended to be higher in p53+ l
ymphomas, A positive correlation existed between mRNA expression of hTERT,
hTER and Tankyrase. hTERT mRNA expression tended to be higher with increasi
ng levels of apoptosis and proliferation, in HG-NHL samples lacking BAX exp
ression and in samples from patients with survival shorter than 3.5 years,
hTER mRNA expression was significantly higher in BAX and BAK negative sampl
es.
Interpretation and Conclusions. Telomerase is activated or upregulated in t
he majority of HG-NHL, Enhanced TA combined with deregulation of the factor
s responsible for cell survival and proliferation may contribute to the dev
elopment and progression of lymphomas. Observation that high hTERT mRNA exp
ression may be related to shorter survival should prompt further investigat
ion of the clinical significance of TA and its components in HG-NHL. (C) 20
01, Ferrata Storti Foundation.