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Expression of molecular targets for tyrosine kinase antagonists in malignant endocrine pancreatic tumors
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinska vetenskaper.
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinska vetenskaper. (Endokrin tumörbiologi)
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinska vetenskaper. (Onkologisk endokrinologi)
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinska vetenskaper. (Endokrin tumörbiologi)
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2003 (engelsk)Inngår i: Clinical Cancer Research, ISSN 1078-0432, E-ISSN 1557-3265, Vol. 9, nr 4, s. 1469-1473Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

PURPOSE:

Molecular targeting with monoclonal antibodies and tyrosine kinase inhibitors is a novel approach to cancer treatment. We have examined the expression of molecular targets in patients with malignant endocrine pancreatic tumors, which is necessary to justify additional studies investigating the potential benefit from such treatment.

EXPERIMENTAL DESIGN:

Thirty-eight tumor tissues from malignant endocrine pancreatic tumors were examined with immunohistochemistry using specific polyclonal antibodies with regard to the expression pattern of platelet-derived growth factor receptors (PDGFRs) alpha and beta, c-kit, and epidermal growth factor receptor (EGFR).

RESULTS:

All 38 tissue specimens expressed PDGFRalpha on tumor cells, and 21 of 37 specimens (57%) expressed PDGFRalpha in tumor stroma (1 specimen was nonevaluable). Twenty-eight samples (74%) stained positive for PDGFRbeta on tumor cells, and 36 of 37 samples (97%) stained positive for PDGFRbeta in the stroma (1 specimen was nonevaluable). Thirty-five tumor tissues (92%) stained positive for c-kit, and 21 (55%) stained positive for EGFR on tumor cells. No differences were seen between syndromes or between poorly differentiated or well-differentiated tumors. Previous treatment did not influence expression pattern. Receptor expression pattern varied considerably between individuals.

CONCLUSIONS:

We have found that tyrosine kinase receptors PDGFRs alpha and beta, EGFR, and c-kit are expressed in more than half of the patients with endocrine pancreatic tumors. Because these receptors represent molecular targets for STI571 and ZD1839 (tyrosine kinase inhibitors) and IMC-C225 (a monoclonal antibody), we propose that patients suffering from EPTs might benefit from this new treatment strategy. However, because of great variability in receptor expression pattern, all patients' individual receptor expression should be examined.

sted, utgiver, år, opplag, sider
2003. Vol. 9, nr 4, s. 1469-1473
HSV kategori
Identifikatorer
URN: urn:nbn:se:uu:diva-90041PubMedID: 12684421OAI: oai:DiVA.org:uu-90041DiVA, id: diva2:162080
Tilgjengelig fra: 2002-10-24 Laget: 2002-10-24 Sist oppdatert: 2017-12-14bibliografisk kontrollert
Inngår i avhandling
1. Current Medical Treatment of Endocrine Pancreatic Tumors and Future Aspects
Åpne denne publikasjonen i ny fane eller vindu >>Current Medical Treatment of Endocrine Pancreatic Tumors and Future Aspects
2002 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

We treated 16 patients with somatostatin analogs combined with α-interferon and achieved a biochemical and/or radiological response in 56% (median duration 22 months). We consider this treatment a good alternative for patients who fail during chemotherapy or who do not want to/cannot receive cytotoxic drugs.

Thirty-six patients with neuroendocrine tumors were treated with cisplatin combined with etoposide. Of 14 patients with evaluable EPTs, 50% responded radiologically and/or biochemically (median duration 9 months). We consider this treatment useful as first-line medical treatment in aggressive EPTs or in patients failing prior chemotherapy.

Twenty-eight tumor tissues from EPTs were examined with immunohistochemistry regarding expression of somatostatin receptors (ssts) 1 to 5 on tumor cells and in intratumoral vessels. We found that sst2 and sst4 were highly expressed on tumor cells and in vessels. However, sst3 and sst5 were lacking in half of the tumor tissues and in most of the vessels. Because of the variability in sst expression, we recommend analysis of each individual’s receptor expression before starting treatment.

Endocrine pancreatic tumors (EPTs) are rare with an incidence of 4 per million inhabitants. In the majority of cases they grow slowly, but there are exceptions with very rapidly progressing malignant carcinomas. First-line medical treatment is streptozotocin combined with 5-fluorouracil.

We examined 38 tumor samples regarding expression of tyrosine kinase receptors platelet-derived growth factor receptors (PDGFRs), c-kit and epidermal growth factor receptor (EGFR). We found that the receptors were expressed in more than half of the tumor tissues. Further studies will reveal if tyrosin kinase antagonists can be part of the future treatment arsenal.

sted, utgiver, år, opplag, sider
Uppsala: Acta Universitatis Upsaliensis, 2002. s. 71
Serie
Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 0282-7476 ; 1191
Emneord
Medical sciences, pancreatic tumors, somatostatin analogs, cisplatin, etoposide, somatostatin receptors, immunohistochemistry, tyrosine kinase receptors, platelet-derived growth factors receptors (PDGFRs), c-kit, epidermal growth factor receptor (EGFR), MEDICIN OCH VÅRD, alfa-interferon
HSV kategori
Forskningsprogram
medicin
Identifikatorer
urn:nbn:se:uu:diva-2709 (URN)91-554-5424-0 (ISBN)
Disputas
2002-11-16, Aulan, ingång 50, Akademiska sjukhuset, Uppsala, 09:15
Opponent
Tilgjengelig fra: 2002-10-24 Laget: 2002-10-24bibliografisk kontrollert

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