Heterogeneous response to the growth factors [EGF, PDGF (bb), TGF‐α, bFGF, IL‐2] on glioma spheroid growth, migration and invasion

Paal‐Henning ‐H Pedersen*, Gro Oddveig Ness, Olav Engebraaten, Rolf Bjerkvig, Johan R. Lillehaug, Ole Didrik Laerum

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

80 Citations (Scopus)

Abstract

The effects of 5 different growth factors [EGF, PDGF(bb), TGF‐α, bFGF and IL‐2] were studied on tumour spheroids obtained from 5 different human glioma cell lines (U‐251MG, D‐263MG, D‐37MG, D‐54MG, GaMG). The expression of EGF and PDGF receptors as well as the endogenous production of TGF‐α and PDGF Were studied by Northern blot analyses. After growth‐factor‐exposure, tumour spheroid volume growth, and directional cell migration from the spheroids were studied. In addition, tumour‐cell invasion was studied In vitro, where foetal rat‐brain aggregates were used as a target for the tumour cells. In all the assays a common stimulator for most of the cell lines was EGF. The other growth factors had a more heterogeneous stimulatory effect. Tumour‐cell invasion, cell growth and cell migration are biological properties which are not necessarily related to each other. This may explain why the tumours often responded differently to the growth factors in the various assay systems. Two of the cell lines studied were non‐invasive (U‐25IMG, D‐263MG). It is shown that these were stimulated both in the directional migration assay and in the spheroid‐volume‐growth assay. However, their non‐invasive behaviour was not influenced by the growth factors studied.

Original languageEnglish
Pages (from-to)255-261
Number of pages7
JournalInternational Journal of Cancer
Volume56
Issue number2
DOIs
Publication statusPublished - 15 Jan 1994
Externally publishedYes

Fingerprint

Dive into the research topics of 'Heterogeneous response to the growth factors [EGF, PDGF (bb), TGF‐α, bFGF, IL‐2] on glioma spheroid growth, migration and invasion'. Together they form a unique fingerprint.

Cite this