Inhibition of programmed cell death (apoptosis) is associated with increase
d tumor aggressiveness. We hypothesized that a novel apoptosis inhibitor ge
ne, antiapoptosis clone 11 (AAC-11), may be expressed in tumors of patients
with non-small cell lung cancer (NSCLC) and affect their clinical outcome.
Expression of AAC-11 messenger RNA was evaluated by reverse transcription
polymerase chain reaction (RT-PCR) in 94 non-small cell lung carcinomas and
adjacent histologically normal lung samples. The data was analyzed in refe
rence to clinicopathological and survival data. AAC-11 transcripts were det
ected in 12 (12.7%) of the tumor samples, although five of paired nor-Mal l
ung samples showed very weak expression. There was no relationship between
AAC-11 gene expression and age, gender, N or T-status. AAC-11 was preferent
ially expressed in squamous cell carcinoma (26.9% of squamous cell carcinom
a vs. 7% of adenocarcinoma). The NSCLC patients with AAC-11 expression had
significantly poor survival than the patients without AAC-11 expression (P=
0.0360). Although the AAC-1 gene was not expressed in a majority of NSCLC t
umors, we suggest that AAC-11 may predict poor survival. (C) 2001 Elsevier
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