Ke. Wilson et al., EXPRESSION OF THE EXTRACELLULAR-MATRIX PROTEIN TENASCIN IN MALIGNANT AND BENIGN OVARIAN-TUMORS, British Journal of Cancer, 74(7), 1996, pp. 999-1004
The extracellular matrix protein tenascin (TN) is overexpressed in a n
umber of solid tumours. This, however, is the first study to examine T
N expression in ovarian tumours. TN protein was examined in frozen sec
tions of 50 human ovarian tumours by immunohistochemistry. Malignant a
nd borderline tumours showed a significantly greater incidence and int
ensity of stromal staining than benign tumours (P < 0.0001 and P = 0.0
38 respectively). Seven omental metastases were also examined and show
ed a strikingly similar protein distribution to their primary tumour c
ounterparts. The expression pattern of different RNA isoforms, created
by alternative splicing of the primary transcript, was identified usi
ng reverse transcription-polymerase chain reactions (RT-PCR). The smal
lest TN RNA splice variant (284 bp) was found in all tumours examined,
while the appearance of larger molecular weight transcripts (similar
to 490 and 556 bp), as major forms, was predominantly limited to malig
nant tumours, with 9/12 malignant tumours showing this pattern compare
d with 1/6 benign tumours. These data suggest that malignant ovarian t
umours have increased expression of TN compared with benign tumours an
d this may be associated with induction of specific isoforms.