Exposure of human proliferative cells to subcytotoxic stress triggers stress-induced premature senescence (SIPS) which is characterized by many biomarkers of replicative senescence. Proteomic comparison of replicative senescence and stress-induced premature senescence indicates that, at the level of protein expression, stress-induced premature senescence and replicative senescence are di¡erent phenotypes sharing however similarities. In this study, we identi¢ed 30 proteins showing changes of expression level speci¢c or common to replicative senescence and/or stress-induced premature senescence. These changes a¡ect di¡erent cell functions, including energy metabolism, defense systems, maintenance of the redox potential, cell morphology and transduction pathways. ß 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.