U. Wulbrand et al., mRNA expression patterns of insulin-like growth factor system components in human neuroendocrine tumours, EUR J CL IN, 30(8), 2000, pp. 729-739
Citations number
47
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research General Topics
Background Insulin-like growth factors (IGF) and their corresponding recept
ors and binding proteins are important in carcinogenesis for several rumour
s, but their expression pattern in the functionally and biologically hetero
geneous human neuroendocrine rumours of the gastroenteropancreatic tract is
largely unknown.
Materials and methods This study searched for the mRNA expression patterns
of components of the IGF system: IGF-1 and IGF-2, IGF receptors 1 and 2 (IG
F-1R, IGF-2R), IGF-binding proteins 1-6 (IGFBP1-6)) in the most frequent hu
man gastroenteropancreatic neuroendocrine tumours (gastrinomas, insulinomas
, tumours associated with carcinoid syndrome and functionally inactive tumo
urs) employing reverse transcriptase-polymerase chain reaction (RT-PCR).
Results In the 37 tumour samples analysed (nine gastrinomas, 10 insulinomas
, nine tumours associated with carcinoid syndrome and nine functionally ina
ctive rumours) IGFBP-2 was found in all tumour samples while the IGFBP-1 wa
s expressed only at low frequency (10-22%) among the four tumour types. The
IGF-2R was predominantly expressed in gastrinomas. Among the four tumour t
ypes the expression of IGF-1R, IGF-2R and IGFBP-6 varied significantly. In
addition, 12 pairs of significantly coexpressed IGF system components were
detected (IGF-1 <----> IGF-1R, IGF-1 <----> IGF-2R, IGF-1 <----> IGFBP-3, I
GF-1 <----> IGFBP-6, IGFBP-3 <----> IGF-1R, IGFBP-6 <----> IGF-1R, IGFBP-1
<----> IGF-2R, IGFBP-3 <----> IGF-2R, IGFBP-5 <----> IGF-2R, IGFBP-3 <---->
IGFBP-5, IGFBP-3 <----> IGFBP-6, IGFBP-5 <----> IGFBP-6).
Conclusions The described differences of the expression patterns of the IGF
system components in neuroendocrine tumour subtypes suggest tumour type-de
pendent different pathways in tumour growth control by IGF system component
s.