The Journal of Pathology · 1998 · 43 citations · 27 references
MedicineCancer BiologyOncologyNeoplasiaOncogenesSignal TransductionCancer BiomarkersCancer Cell SignalingGrowth Factor Receptor OncogenesThyroid CancerTumor MarkersPapillary Thyroid Carcinoma PathologyPlasminogen ActivatorsThyroid AdenomasThyroid Cancer Pathology
Met protein encoded by MET oncogene is the high affinity receptor for hepatocyte growth factor (HGF)/scatter factor (SF). HGF/SF has to be cleaved in its heterodimeric form by the urokinase-type plasminogen activator (uPA) to become active as a ligand for Met receptor. The expression of Met protein and of the high affinity receptor for uPA (uPA-R) was investigated in 39 samples of papillary carcinoma using immunohistochemistry. Reactivity for Met protein was present in 33 of 34 tumours, mostly with a diffuse pattern of staining. Reactivity for uPA-R was present in 78 per cent of papillary tumours and exhibited a pattern of staining similar to that of Met protein. Staining for uPA-R was present in 23 of 25 cases (92 per cent) of papillary carcinoma with prominent sclerosis, and in only 1 of 7 cases (14 per cent) without sclerosis. Peritumoural normal thyroid, follicular adenomas, and follicular carcinomas were negative for Met protein and for uPA-R. Hyperfunctioning tall thyroid cells showed weak membrane reactivity for uPA-R and for Met protein. The findings of immunohistochemistry were confirmed at the mRNA level using in situ hybridization, since the signal for uPA-R and Met RNAs was detected in most tumour cells of five cases of papillary carcinoma.
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Michael Ploug, Ebbe Rønne, Niels Behrendt et al. · Journal of Biological Chemistry · 1991 · 580 citations · Full text