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. 2010 Oct 20;102(20):1536–1546. doi: 10.1093/jnci/djq364

Table 2.

Drugs that induce senescence in cancer cell lines and tumors*

Agent p53 status Mechanism In vitro In vivo§ Reference
Aphidocolin + DNA polymerase inhibitor + (9)
Bleomycin + DNA damage + (64)
Camptothecin +/− DNA damage + (65)
Carboplatin + docetaxel +/− DNA damage + Human lung tumors (18)
Cisplatin +/− DNA damage + (9)
Cyclophosphamide + doxorubicin + 5-Fluorouracil DNA damage Human breast tumors (19)
Diaziquone/AZQ +/− DNA damage + Prostate xenograft tumors (13)
Doxorubicin +/− DNA damage + (9)
Epigallocatechin gallate + Telomerase inhibition + (66)
Etoposide +/− DNA damage + (9)
Gamma irradiation +/− DNA damage + + (10)
Hydroxyurea + ROS + (67)
K858 +/− KIF11 + Xenografts tumors (68)
Lovastatin HMG-CoA-reductase inhibitor + (69)
Mitoxantrone +/− DNA damage + Human prostate tumors (70)
MLN4924 −/+ Cul1 SCF subunit inhibitor + Prostate xenografts tumors
MLN8054 + Aurora kinase A inhibitor + Colon xenograft tumors (28)
Pyrithione +/− Zinc/calcium regulation, ROS + (13)
Resveratrol + ROS + (71)
Retinols + Differentiation + (9)
TPA, PEP005, PEP008 + PKC activating + (59,60)
VO-OHpic + PTEN + Prostate xenograft tumors (29)
*

Cul1= cullin 1; HMG-Co-A reductase = 3-hydroxy-3-methylglutaryl-CoA-reductase; KIF11 = kinesin family member 11; PKC = protein kinase C; PTEN = phosphatase and tensin homolog; ROS = reactive oxygen species; SCF = Skp1/Cul1/F-box protein complex.

p53 status of cells in which the drug induces senescence. (+) denotes active p53 in cancer cells in which the drug induces senescence, whereas (−) denotes senescence induction by the drug in cancer cells in which p53 is deleted or mutated.

Senescence-inducing activity of drug in cancer cells in vitro; (+) denotes induction of senescence in vitro, whereas an empty cell denotes that results were not determined.

§

Senescence-inducing activity of drug in vivo in patients or tumor models. An empty cell denotes that results are not determined; (+) denotes senescence induction in various in vivo tumor models.