3416400802

3416400802



1360    I. J. Radiation Oncology • Biology • Physics

Table 1. Radiosensitivity paramcters (SF?, a, and fi) calculalcd using the linear-quadratic model in KB and KB3 ccii lincs cxposed to dcxamethasone (DEX, 10_oM, 24 h) or TNFa (2.5

ng/mL, 10 min)

Celi lines

KB

KB3

Control

DEX

Control

TNFa

sf2*

0.799*

0.758

0.480

0.632

a

0.052

0.114

0.064

0.054

fi

0.030

0.012

0.151

0.087

* Surviving fraction at 2 Gy. y Mean valucs of thrcc independent expcriments. Notę: Standard deviations were less than 15%.

Volumc 51, Numbcr 5, 2001

pathway. A similar observation has been dcscribed al-ready in Hodgkin’s lymphoma cells, which were pro-tected from irradiation without a dccreasc in NF-kB activity in the prescncc of DEX (28).

This study demonstrates that the constitutive NF-kB level influences the intrinsic radiosensitivity of the KB and KB3 celi lines. Morcovcr, if our work does not formally involve anti-apoptotic activities of NF-kB in resistance to radiotherapy, it certainly indicates that this transcription factor plays a central role in basal intrinsic radiosensitivity and could protect cells against apoptosis, probably by controlling the expression of apoptosis inhibitors. Modulation of this basal level could be recommended bcforc ionizing radiation ex-posure to inerease radiotherapy response.

REFERENCES

1.    Wilson RE, Taylor SL, Atherton GT, et al. Early response gene signalling cascadcs activated by ionising radiation in primary human B cells. Oncogene 1993;8:3229-3237.

2.    Mohan N, Meltz ML. Induction of nuclear factor kappa B after low-dosc ionizing radiation involves a rcactive oxygen inter-mediate signaling pathway. Radiat Res 1994;140:97-104.

3.    Yamagishi N, Miyakoshi J, Takebc H. Enhanced radioscnsitivity by inhibition of nuclear factor kappa B activation in human malignant glioma cells. Int./ Radiat Biol. 1997;72:157-162.

4.    Pajonk F, Pajonk K, McBride Wll. Inhibition of NF-kappaB, clonogcnicily, and radiosensitivity of human cancer cells. J Natl Cancer Inst 1999;91:1956-1960.

5.    Lezoualc’h F, Sagara Y, Holsboer F, et al. High constitutive NF-kappaB activity mediates resistance to oxidativc stress in neuronal cells. J Neurosci 1998;18:3224-3232.

6.    Wang CY, Mayo MW, Komcluk RG, et al. NF-kappaB anti-apoptosis: Induction of TRAFI and TRAF2 and c-IAPl and C-IAP2 to suppress caspasc-8 activalion. Science 1998;281: 1680-1693.

7.    Kaltschmidt B, Kaltschmidt C, Hofmann TG, et al. The pro- or anti-apoptotic function of NF-kappaB is determined by the naturę of the apoptotic stimulus. Eur J Biochem 2000;267:3828-3835.

8.    Bcg AA, Baltimore D, An csscntial role for NF-kappaB in prcventing TNF-alpha-induced celi dcath. Science 1996;274:782-784.

9.    Suzuki A, Tsutomi Y, Akahane K et al. Resistance to Fas-mediated apoptosis: Activation of caspasc 3 is regulated by celi cyclc regulator p21WAFl and IAP gene family ILP. Oncogene 1998; 17:931 -939.

10.    Javelaud D, Wictzerbin J, Delattre O, et al. Induction of p21 Wafl/Cipl by TNFalpha requires NF-kappaB activity and antagonizes apoptosis in Ewing tumor cells. Oncogene 2000; 19:61-68.

11.    Jung M, Zhang Y, Lee S, et al. Correction of radiation sensitivity in ataxia tclangiectasia cells by a truncatcd I kappa B-alpha. Science 1995;268:1619-1621.

12.    Lcvinc EL. Davidson SE, Robcrts SA et al. Apoptosis as prediclor of response to radiotherapy in ccrvical carcinoma (lettcrj. Lancet 1994;344:472.

13.    Alkalay I, Yaron A, Hatzubai A, et al. Stimulation-dependcnt I kappa B alpha phosphorylation marks the NF-kappa B inhibitor for degradalion via the ubiquitin-proteasome pathway. Proc Natl Acad Sci USA. 1995;92:10599 -10603.

14.    Schcrer DC, Brockmań JA, Chenr Z, et al. Signal-induccd degradation of I kappa B alpha requires site-specific ubicjuiti-nation. Proc Natl Acad Sci USA I995;92:11259-11263.

15.    Baeuerle PA, Baltimore D. NF-kappa B: Ten years after. Celi 1996;87:13-20.

16.    Didclot C, Mirjolel JF, Barbcri-Heyob, M et al. Influence of S-phase duration on G2 arrest-mediated apoptosis induction by radiations in celi lines exprcssing differenl level of sensi-tivily to 5-fluorouracil (5FU). Proc Amer Assoc Cancer Res 2000;41:785.

17.    Dignain JD, Lebovitz RM, Rocdcr RG. Accurate transcription initiation by RN A polymerase II in a soluble extract from isolated mam mai i an nuclci. Nucleic Acids Res 1983;! 1:1475-1489.

18.    Lowry OH, Rosenbrough NJ, Farr AR, et al. Protein measure-ment with the Folin phenol reagent. J Biol Chem 1951; 193; 265-275.

19.    Griffon Etiennc G, Merlin JL, Marchal C. In vitro evaluation of Taxol combined with radiations in human squamous celi carcinoma sphcroids. Cancer Lett 1996;109:23-32.

20.    Thames HD, Jr., Rozell ME, Tuckcr SL, et al. Direct analysis of quantal radiation response data. Int J Radiat Biol Relat Stud Phys Chem Med 1986;49:999-1009.

21.    Auphan N, Di Donato, JA, Roscttc C, et al. Jmmunosuppression by glucocorticoids: Inhibition of NF-kappa B activity through induction of I kappa B synthesis. Science 1995;270:286-290.

22.    Mcrcurio F. Zhu H, Murray BW, et al. IKK-1 and IKK-2: Cytokine-activatcd IkappaB kinases cssenlial for NF-kappaB activation. Science 1997;278:860-866.

23.    Van Antwcrp DJ, Martin SJ, Kafri T, et al. Supprcssion of TNF-alpha-induced apoptosis by NF-kappaB. Science 1996; 274:787-789.

24.    Wang CY, Cusack JC, Jr., Liu R et al. Control of inducible chemoresistance: Enhanced anti-tumor therapy through in-creascd apoptosis by inhibition of NF-kappaB. Nat Med 1999; 5:412-417.

25.    Liu ZG, Hsu H, Goeddel DV, et al. Dissection of TNF receptor 1 effector functions: JNK activation is not linked to apoptosis while NF-kappaB activation prevents celi death. Celi 1996;87:565-576.

26.    Bentires-Alj M, Hellin AC, Ameyar M, et al. Stable inhibition of nuclear factor kappaB in cancer cells does not inerease sensitivity to cytotoxic drugs. Cancer Res 1999;59:811-815.

27.    Zong WX. Edelstein LC. Chcn C et al. The prosurviva! Bcl-2 homolog Bfl-l/Al is a direct transcriptional target of NF-kappaB that blocks TNFalpha-induced apoptosis. Genes Dev 1999;13:382-387.

28.    Pajonk F, Pajonk K, McBride WH. Apoptosis and radiosen-sitization of hodgkin cells by proteasome inhibition. Int J Radiat Oncol Biol Phys 2000;47:1025-1032.



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