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锰超氧化物歧化酶对5-氟尿嘧啶、培洛霉素和γ射线诱导的鳞状细胞癌细胞凋亡具有负向调节作用。

Manganese superoxide dismutase negatively regulates the induction of apoptosis by 5-fluorouracil, peplomycin and gamma-rays in squamous cell carcinoma cells.

作者信息

Ueta E, Yoneda K, Yamamoto T, Osaki T

机构信息

Department of Oral Surgery, Kochi Medical School, Nankoku-city.

出版信息

Jpn J Cancer Res. 1999 May;90(5):555-64. doi: 10.1111/j.1349-7006.1999.tb00783.x.

Abstract

We investigated the relationship between manganese superoxide dismutase (Mn-SOD) activity and apoptosis induced by anticancer drugs and radiation. Although the activity of copper, zinc-SOD did not differ greatly among 9 squamous cell carcinoma (SCC) cell lines (OSC-1 to OSC-9), the Mn-SOD activity did differ among the cell lines. The Mn-SOD activity was increased by treatments with 5-fluorouracil (5-FU), peplomycin and 137Cs, reaching plateau levels at 12 h after treatment and then decreasing gradually. When OSC-1 and OSC-3, and OSC-2 and OSC-4 were examined as representative cell lines with low and high Mn-SOD activity, respectively, the decrease was more prominent in OSC-1 and OSC-3 than in OSC-2 and OSC-4. The intracellular levels of superoxide and hydrogen peroxide (H2O2) were increased after treatment with the anticancer agents, and the increases were larger in OSC-1 and OSC-3 than in OSC-2 and OSC-4. The decrease of mitochondrial membrane potential (deltapsi(m)) by the anticancer agents was marked in OSC-1 and OSC-3. Correspondingly, the release of cytochrome c, the activation of caspase-3 and the cleavage of poly(ADP-ribose)polymerase were stronger in OSC-3 than in OSC-4. In addition, apoptosis induced by the anticancer agents was prominent in OSC-3, exhibiting a close relationship with the deltapsi(m) and the H2O2 level. These results indicate that Mn-SOD in SCC cells modulates apoptosis induction and the inactivation of Mn-SOD might be a promising strategy for SCC treatment.

摘要

我们研究了锰超氧化物歧化酶(Mn-SOD)活性与抗癌药物及辐射诱导的细胞凋亡之间的关系。尽管9种鳞状细胞癌(SCC)细胞系(OSC-1至OSC-9)中铜锌超氧化物歧化酶(Cu,Zn-SOD)的活性差异不大,但Mn-SOD活性在各细胞系中存在差异。用5-氟尿嘧啶(5-FU)、培普利霉素和137Cs处理后,Mn-SOD活性升高,在处理后12小时达到平台期水平,然后逐渐下降。当分别以Mn-SOD活性低和高的代表性细胞系OSC-1和OSC-3,以及OSC-2和OSC-4进行检测时,OSC-1和OSC-3中的下降比OSC-2和OSC-4更明显。抗癌药物处理后,细胞内超氧阴离子和过氧化氢(H2O2)水平升高,OSC-1和OSC-3中的升高比OSC-2和OSC-4更大。抗癌药物引起的线粒体膜电位(ΔΨm)下降在OSC-1和OSC-3中更为明显。相应地,细胞色素c的释放、caspase-3的激活以及聚(ADP-核糖)聚合酶的裂解在OSC-3中比在OSC-4中更强。此外,抗癌药物诱导的细胞凋亡在OSC-3中更为突出,与ΔΨm和H2O2水平密切相关。这些结果表明,SCC细胞中的Mn-SOD调节细胞凋亡诱导,Mn-SOD的失活可能是SCC治疗的一种有前景的策略。

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本文引用的文献

1
Protein measurement with the Folin phenol reagent.
J Biol Chem. 1951 Nov;193(1):265-75.
3
Molecular cloning and characterization of human caspase-activated DNase.
Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9123-8. doi: 10.1073/pnas.95.16.9123.
4
Endotoxin pretreatment in vivo increases the mitochondrial respiratory capacity in rat hepatocytes.
Arch Biochem Biophys. 1998 Jun 1;354(1):9-17. doi: 10.1006/abbi.1998.0699.
5
Apoptosis induction by caspase-8 is amplified through the mitochondrial release of cytochrome c.
J Biol Chem. 1998 Jun 26;273(26):16589-94. doi: 10.1074/jbc.273.26.16589.
6
The regulation of reactive oxygen species production during programmed cell death.
J Cell Biol. 1998 Jun 15;141(6):1423-32. doi: 10.1083/jcb.141.6.1423.
7
8
Antioxidant action via p53-mediated apoptosis.
Cancer Res. 1998 Apr 15;58(8):1723-9.
9
Induction of the mitochondrial permeability transition causes release of the apoptogenic factor cytochrome c.
Free Radic Biol Med. 1998 Mar 1;24(4):624-31. doi: 10.1016/s0891-5849(97)00367-5.
10
Acute promyelocytic leukemia: cellular and molecular basis of differentiation and apoptosis.
Pharmacol Ther. 1997 Oct-Dec;76(1-3):141-9. doi: 10.1016/s0163-7258(97)00090-9.

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