transforming-growth-factor-alpha and Paraganglioma

transforming-growth-factor-alpha has been researched along with Paraganglioma* in 1 studies

Other Studies

1 other study(ies) available for transforming-growth-factor-alpha and Paraganglioma

ArticleYear
Expression of transforming growth factor alpha and its receptor in human neuroendocrine tumours.
    International journal of cancer, 1995, Mar-03, Volume: 60, Issue:5

    Transforming growth-factor-alpha (TGF-alpha) is a 50-amino-acid polypeptide that binds to the epidermal growth factor (EGF) receptor and stimulates cell growth. It has been suggested that enhanced production of TGF-alpha and EGF receptors by tumour cells promote tumour-cell growth by autocrine mechanisms. In the present study we have investigated the expression of TGF-alpha and EGF receptors in human neuroendocrine tumours, including midgut carcinoid tumours, phaeochromocytomas and medullary thyroid carcinomas. TGF-alpha expression was demonstrated in biopsies of all tumours examined (n = 30) and EGF receptors in a majority of tumours by Northern analysis and/or immunocytochemistry. Expression of TGF-alpha and EGF receptors was also demonstrated in primary cultures of tumour cells. Carcinoid tumours and phaeochromocytomas in culture secreted detectable amounts of TGF-alpha into the culture medium (400-700 pM). The amount of secreted TGF-alpha could be suppressed by octreotide treatment in individual tumours. Administration of exogenous TGF-alpha stimulated carcinoid tumour growth in vitro as determined by the DNA contents of cell cultures. The growth-stimulatory effect of TGF-alpha could be partially blocked by the use of neutralizing anti-EGF receptor monoclonal antibodies (MAbs). In conclusion, several human neuroendocrine tumours express both TGF-alpha and EGF receptors in in vivo and in vitro, suggesting that TGF-alpha may regulate tumour-cell growth by autocrine mechanisms.

    Topics: Adrenal Gland Neoplasms; Aged; Antibodies, Monoclonal; Autoreceptors; Carcinoid Tumor; Carcinoma, Medullary; Cell Division; DNA, Neoplasm; ErbB Receptors; Female; Gene Expression Regulation, Neoplastic; Humans; Liver Neoplasms; Lymphatic Metastasis; Male; Middle Aged; Neoplasm Proteins; Neuroendocrine Tumors; Paraganglioma; Pheochromocytoma; Retroperitoneal Neoplasms; RNA, Messenger; RNA, Neoplasm; Thyroid Neoplasms; Transforming Growth Factor alpha; Tumor Cells, Cultured

1995