Survival signals within the tumour microenvironment suppress drug- induced apoptosis: Lessons learned from B lymphomas

Abstract

The suppression of apoptosis is one mechanism by which tumours become drug resistant. Extracellular signals from the germinal centre (GC) of secondary lymphoid tissue can rescue B cells from physiological- and chemotherapy-induced apoptosis. Such survival signals include CD40 receptor ligation, interleukin-4 (IL-4) receptor stimulation and the interaction of the integrin ligand VCAM-1 with its receptor. The GC environment was modelled in vitro by providing B lymphoma cells with these survival signals. JLP119 B lymphoma cells underwent apoptosis after exposure to the topisomerase II inhibitor etoposide and this was dramatically reduced when the cells were cultured in the GC system. CD40 receptor ligation resulted in increased levels of Bcl-X(L). Etoposide diminished the binding between Bax and Bcl- X(L) but this was restored by IL-4 and VCAM-1 triggered signals. These data demonstrate combined effects of three microenvironmental signals on the Bcl- 2 family and illustrate the potential importance of such signalling pathways in drug resistance of tumour cells.