
Reactive oxygen species generation is essential for cisplatin-induced accelerated senescence in hepatocellular carcinoma
Frontiers of Medicine ›› 2014, Vol. 8 ›› Issue (2) : 227-235.
Reactive oxygen species generation is essential for cisplatin-induced accelerated senescence in hepatocellular carcinoma
Accelerated senescence is important because this process is involved in tumor suppression and has been induced by many chemotherapeutic agents. The platinum-based chemotherapeutic agent cisplatin displays a wide range of antitumor activities. However, the molecular mechanism of cisplatin-induced accelerated senescence in hepatocellular carcinoma (HCC) remains unclear. In the present study, the growth inhibitory effect of cisplatin on HepG2 and SMMC-7721 cells was detected by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Cellular senescence was then assessed by β-galactosidase assay. Senescence-related factors, including p53, p21, and p16, were evaluated by quantitative reverse transcription-polymerase chain reaction. Reactive oxygen species (ROS) was analyzed by flow cytometry. Our results revealed that cisplatin reduced the proliferation of HepG2 and SMMC-7721 cells in a dose- and time-dependent manner. Senescent phenotype observed in cisplatin-treated hepatoma cells was dependent on p53 and p21 activation but not on p16 activation. Furthermore, cisplatin-induced accelerated senescence depended on intracellular ROS generation. The ROS scavenger N-acetyl-L-cysteine also significantly suppressed the cisplatin-induced senescence of HepG2 and SMMC-7721 cells. In conclusion, our results revealed a functional link between intracellular ROS generation and cisplatin-induced accelerated senescence, and this link may be used as a potential target of HCC.
reactive oxygen species / senescence / cisplatin / hepatocellular carcinoma
[1] |
HayflickL. The limited in vitro lifetime of human diploid cell strains. Exp Cell Res1965; 37(3): 614-636
CrossRef
ADS
Pubmed
Google scholar
|
[2] |
DimriGP, LeeX, BasileG, AcostaM, ScottG, RoskelleyC, MedranoEE, LinskensM, RubeljI, Pereira-SmithO. A biomarker that identifies senescent human cells in culture and in aging skin in vivo. Proc Natl Acad Sci USA1995; 92(20): 9363-9367
CrossRef
ADS
Pubmed
Google scholar
|
[3] |
ChangBD, BroudeEV, DokmanovicM, ZhuH, RuthA, XuanY, KandelES, LauschE, ChristovK, RoninsonIB. A senescence-like phenotype distinguishes tumor cells that undergo terminal proliferation arrest after exposure to anticancer agents. Cancer Res1999; 59(15): 3761-3767
Pubmed
|
[4] |
te PoeleRH, OkorokovAL, JardineL, CummingsJ, JoelSP. DNA damage is able to induce senescence in tumor cells in vitro and in vivo. Cancer Res2002; 62(6): 1876-1883
Pubmed
|
[5] |
FangK, ChiuCC, LiCH, ChangYT, HwangHT. Cisplatin-induced senescence and growth inhibition in human non-small cell lung cancer cells with ectopic transfer of p16INK4a. Oncol Res2007; 16(10): 479-488
CrossRef
ADS
Pubmed
Google scholar
|
[6] |
WangX, WongSC, PanJ, TsaoSW, FungKH, KwongDL, ShamJS, NichollsJM. Evidence of cisplatin-induced senescent-like growth arrest in nasopharyngeal carcinoma cells. Cancer Res1998; 58(22): 5019-5022
Pubmed
|
[7] |
PanieriE, GogvadzeV, NorbergE, VenkateshR, OrreniusS, ZhivotovskyB. Reactive oxygen species generated in different compartments induce cell death, survival, or senescence. Free Radic Biol Med2013; 57: 176-187
CrossRef
ADS
Pubmed
Google scholar
|
[8] |
LiSK, SmithDK, LeungWY, CheungAM, LamEW, DimriGP, YaoKM. FoxM1c counteracts oxidative stress-induced senescence and stimulates Bmi-1 expression. J Biol Chem2008; 283(24): 16545-16553
CrossRef
ADS
Pubmed
Google scholar
|
[9] |
QuK, XuX, LiuC, WuQ, WeiJ, MengF, ZhouL, WangZ, LeiL, LiuP. Negative regulation of transcription factor FoxM1 by p53 enhances oxaliplatin-induced senescence in hepatocellular carcinoma. Cancer Lett2013; 331(1): 105-114
CrossRef
ADS
Pubmed
Google scholar
|
[10] |
RobersonRS, KussickSJ, VallieresE, ChenSY, WuDY. Escape from therapy-induced accelerated cellular senescence in p53-null lung cancer cells and in human lung cancers. Cancer Res2005; 65(7): 2795-2803
CrossRef
ADS
Pubmed
Google scholar
|
[11] |
ColavittiR, FinkelT. Reactive oxygen species as mediators of cellular senescence. IUBMB Life2005; 57(4-5): 277-281
CrossRef
ADS
Pubmed
Google scholar
|
[12] |
IshikawaF. Cellular senescence, an unpopular yet trustworthy tumor suppressor mechanism. Cancer Sci2003; 94(11): 944-947
CrossRef
ADS
Pubmed
Google scholar
|
[13] |
ColladoM, GilJ, EfeyanA, GuerraC, SchuhmacherAJ, BarradasM, BenguríaA, ZaballosA, FloresJM, BarbacidM, BeachD, SerranoM. Tumour biology: senescence in premalignant tumours. Nature2005; 436(7051): 642
CrossRef
ADS
Pubmed
Google scholar
|
[14] |
ColladoM, SerranoM. Senescence in tumours: evidence from mice and humans. Nat Rev Cancer2010; 10(1): 51-57
CrossRef
ADS
Pubmed
Google scholar
|
[15] |
XueW, ZenderL, MiethingC, DickinsRA, HernandoE, KrizhanovskyV, Cordon-CardoC, LoweSW. Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas. Nature2007; 445(7128): 656-660
CrossRef
ADS
Pubmed
Google scholar
|
[16] |
JonesKR, ElmoreLW, Jackson-CookC, DemastersG, PovirkLF, HoltSE, GewirtzDA. p53-Dependent accelerated senescence induced by ionizing radiation in breast tumour cells. Int J Radiat Biol2005; 81(6): 445-458
CrossRef
ADS
Pubmed
Google scholar
|
[17] |
SantarosaM, Del ColL, ToninE, CaragnanoA, VielA, MaestroR. Premature senescence is a major response to DNA cross-linking agents in BRCA1-defective cells: implication for tailored treatments of BRCA1 mutation carriers. Mol Cancer Ther2009; 8(4): 844-854
CrossRef
ADS
Pubmed
Google scholar
|
[18] |
OzturkN, ErdalE, MumcuogluM, AkcaliKC, YalcinO, SenturkS, Arslan-ErgulA, GurB, YulugI, Cetin-AtalayR, YakicierC, YagciT, TezM, OzturkM. Reprogramming of replicative senescence in hepatocellular carcinoma-derived cells. Proc Natl Acad Sci USA2006; 103(7): 2178-2183
CrossRef
ADS
Pubmed
Google scholar
|
[19] |
PetrosWP, BroadwaterG, BerryD, JonesRB, VredenburghJJ, GilbertCJ, GibbsJP, ColvinOM, PetersWP. Association of high-dose cyclophosphamide, cisplatin, and carmustine pharmacokinetics with survival, toxicity, and dosing weight in patients with primary breast cancer. Clin Cancer Res2002; 8(3): 698-705
Pubmed
|
[20] |
SchmittCA, FridmanJS, YangM, LeeS, BaranovE, HoffmanRM, LoweSW. A senescence program controlled by p53 and p16INK4a contributes to the outcome of cancer therapy. Cell2002; 109(3): 335-346
CrossRef
ADS
Pubmed
Google scholar
|
[21] |
ChangBD, XuanY, BroudeEV, ZhuH, SchottB, FangJ, RoninsonIB. Role of p53 and p21waf1/cip1 in senescence-like terminal proliferation arrest induced in human tumor cells by chemotherapeutic drugs. Oncogene1999; 18(34): 4808-4818
CrossRef
ADS
Pubmed
Google scholar
|
[22] |
ChenZ, TrotmanLC, ShafferD, LinHK, DotanZA, NikiM, KoutcherJA, ScherHI, LudwigT, GeraldW, Cordon-CardoC, PandolfiPP. Crucial role of p53-dependent cellular senescence in suppression of Pten-deficient tumorigenesis. Nature2005; 436(7051): 725-730
CrossRef
ADS
Pubmed
Google scholar
|
[23] |
RayessH, WangMB, SrivatsanES. Cellular senescence and tumor suppressor gene p16. Int J Cancer2012; 130(8): 1715-1725
CrossRef
ADS
Pubmed
Google scholar
|
[24] |
SteinGH, DrullingerLF, SoulardA, DulićV. Differential roles for cyclin-dependent kinase inhibitors p21 and p16 in the mechanisms of senescence and differentiation in human fibroblasts. Mol Cell Biol1999; 19(3): 2109-2117
Pubmed
|
[25] |
VigneronA, VousdenKH. p53, ROS and senescence in the control of aging. Aging (Albany NY)2010; 2(8): 471-474
Pubmed
|
[26] |
LimSC, ChoiJE, KangHS, HanSI. Ursodeoxycholic acid switches oxaliplatin-induced necrosis to apoptosis by inhibiting reactive oxygen species production and activating p53-caspase 8 pathway in HepG2 hepatocellular carcinoma. Int J Cancer2010; 126(7): 1582-1595
Pubmed
|
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|
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