Small cell lung cancer (SCLC) is common in men and women, has a very poor p
rognosis, and is therefore a major cause of premature mortality. As such, a
ny prospects for improved therapy are of great significance. The promise of
telomerase as a therapeutic target is now close to realization with extrem
ely encouraging preclinical studies aimed at the RNA component (hTR) of tel
omerase, The rational integration of telomerase therapeutics into clinical
trials will therefore require tumours to be well characterized for hTR expr
ession. Despite the large number of cancer types now characterized for telo
merase or telomerase component gene expression, only a handful of SCLC samp
les have been analysed. Given the major clinical problem with treating SCLC
, we specifically set out to address the issue of hTR expression in neuroen
docrine tumours, Our study covers 91 pulmonary neuroendocrine tumours (62 S
CLC and 29 carcinoid tumours), We present data to show that upregulation of
the RNA component of telomerase occurs in 98% of human SCLCs, Interestingl
y, the less aggressive carcinoid tumours of the lung had a significantly lo
wer frequency of hTR expression (P < 0.01), Importantly, we compare hTR exp
ression in this series to the well characterized biological targets p53 and
BCL2, and show hTR to be expressed more frequently. Therapies directed at
the RNA component of human telomerase are in active development and these d
ata show SCLC to be a prime target for such therapies.