The topology of gene expression space for a set of 12 cancer types is studied
by means of an entropy-like magnitude, which allows the characterization of the
regions occupied by tumor and normal samples. The comparison indicates that the
number of available states in gene expression space is much greater for tumors
than for normal tissues, suggesting the irreversibility of the progression to
the tumor phase. The entropy is nearly constant for tumors, whereas exhibits a
higher variability in normal tissues, probably due to tissue differentiation.
In addition, we show an interesting correlation between the fraction of
available states and the overlapping between the tumor and normal sample
clouds, interpreted as a way of reducing the decay rate to the tumor phase in
more ordered or structured tissues