S. Eklov et al., LACK OF THE LATENT TRANSFORMING GROWTH-FACTOR-BETA BINDING-PROTEIN INMALIGNANT, BUT NOT BENIGN PROSTATIC TISSUE, Cancer research, 53(13), 1993, pp. 3193-3197
Transforming growth factor beta (TGF-beta) is a family of proteins whi
ch act as a potent growth inhibitor for most cell types including epit
helial cells. TGF-beta is synthesized as latent high molecular weight
complexes, composed of TGF-beta, the NH2-terminal part of the TGF-beta
precursor and the third molecule, the latent TGF-beta binding protein
(LTBP). We here ascertain that TGF-beta is expressed in human prostat
ic cancer tissue as well as in cystectomized prostatic tissue and in m
aterials from transurethral resectionS with benign prostatic hyperplas
ia, analyzed by immunohistochemistry. TGF-beta is observed in both epi
thelial cells and stromal cells. No significant correlation was obtain
ed between TGF-beta expression in tumor cells and their degree of diff
erentiation. However, analysis by immunohistochemistry using antibodie
s against LTBP revealed that specimens from histopathologically verifi
ed human prostatic cancer are mostly negative for this molecule, al th
ough it is expressed in cystectomized prostatic and benign prostatic h
yperplasia tissues. These results indicate that in cystectomized prost
atic and benign prostatic hyperplasia tissues, TGF-beta may be produce
d in a complex associated with LTBP; whereas in prostatic carcinoma, T
GF-beta is produced without associating with LTBP. The biological sign
ificance of the production of TGF-beta in relation to LTBP and the pos
sible association with prognosis are discussed.