Ueta E, Yoneda K, Yamamoto T, Osaki T
Department of Oral Surgery, Kochi Medical School, Nankoku-city.
Jpn J Cancer Res. 1999 May;90(5):555-64. doi: 10.1111/j.1349-7006.1999.tb00783.x.
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.
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。