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Differences between transformed cells and their normal counterparts were de
fined by analyzing the cells' three-dimensional distribution of mass. Varia
bles called factors, which explained the covariance of the real variables,
were extracted from the data. We found that factors #4 (sharp, tapering pro
jections) and #12 (rounding up), corresponded to G-protein functions. Then,
the signature-type mass distribution of transformed cells was defined by f
actor values. Agents that caused signature-type mimicry could quantitativel
y shift factor values, for example, those affecting endocytic processing di
sproportionately reduced values of #4. Signature-type reversal was also obs
erved and may be valuable in predicting the efficacy of chemotherapeutic ag
ents.