Background. Hepatocyte growth factor (HGF) is a cytokine that is released a
fter injury. It is a paracrine factor that is produced by mesenchymal cells
; epithelial and endothelial cells respond to HGF through its receptor, the
c-met protein. Hepatocyte growth factor induces cell growth and cell movem
ent and is also highly angiogenic. Evidence from breast cancer patients sug
gests that HGF is a negative prognostic indicator for breast cancer and is
associated with invasive disease.
Methods. We measured the HGF content in tumor tissue from 56 non-small cell
lung cancer patients using the Western blot technique. The amount of HGF i
n tumor extracts was quantitated by densitometry after transfer of proteins
to nitrocellulose and exposure to antibodies. Survival curves were generat
ed based on clinical information obtained for each patient.
Results. Our data indicate that HGF is also a negative prognostic indicator
in lung cancer. As in the study of breast cancer patients, HGF was associa
ted with recurrence and poor survival; the relative risk was seen to increa
se with increasing HGF tumor content. At levels of HGF greater than 100 uni
ts, the relative risk was 10, compared with that in patients with an HGF le
vel of 1 unit. Node-negative patients with an elevated HGF tumor content ha
d a significantly poorer outcome than node-positive patients with a low HGF
tumor content. The same relationship was observed if the patients were str
atified by stage: elevated HGF was associated with stage I patients whose d
isease recurred and who died of their disease, and stage I patients with el
evated HGF had a worse survival than higher stage patients with a low level
of HGF.
Conclusions. These results suggest that elevated HGF may predict a more agg
ressive biology in non-small cell lung cancer patients. The level of HGF ma
y be useful as an indicator of high risk in early stage lung cancer patient
s. (C) 1998 by The Society of Thoracic Surgeons.