A common property of brain rumours is their ability to cause oedema in the
surrounding brain. Oedema forms as a result of a leaky blood-tumour barrier
and persists when the brain fails to clear the excess fluid. It is a signi
ficant source of morbidity and mortality. The principal anatomical componen
t of the blood-brain barrier is the endothelial tight junction which opens
in glioma microvessels. Multiple tight junction proteins have recently been
identified, such as occludin, claudin, ZO-1, ZO-2 and ZO-3. We propose a m
odel to explain tight junction opening in gliomas based on vascular endothe
lial growth factor secretion and loss of tight junction inducing factor pro
duction by tumour cells. The level of expression of the water channel aquap
orin-4 in peritumoural astrocytes may determine the rate of oedema fluid cl
earance. The identification of the molecular mechanisms of brain tumour oed
ema may allow the design of never anti-oedema medications.