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脂质体阿霉素通过增加细胞氧化应激和硝化应激以及加速细胞凋亡途径来增加射频消融诱导的肿瘤破坏。

Liposomal doxorubicin increases radiofrequency ablation-induced tumor destruction by increasing cellular oxidative and nitrative stress and accelerating apoptotic pathways.

机构信息

Laboratory for Minimally Invasive Tumor Therapies, Department of Radiology, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Ave, Boston, MA 02215, USA.

出版信息

Radiology. 2010 Apr;255(1):62-74. doi: 10.1148/radiol.09091196. Epub 2010 Feb 16.

Abstract

PURPOSE

To determine if oxidative and nitrative stress and/or apoptosis contribute to increased coagulation when combining radiofrequency (RF) ablation with liposomal doxorubicin.

MATERIALS AND METHODS

Animal care committee approval was obtained. R3230 mammary adenocarcinomas in Fischer rats were treated with either RF ablation (n = 43), 1 mg of intravenously injected liposomal doxorubicin (n = 26), or combined therapy (n = 30) and were compared with control subjects (n = 11). A subset of animals receiving combination therapy (n = 24) were treated in the presence or absence of N-acetylcysteine (NAC) administered 24 hours and 1 hour before RF ablation. Tumors were analyzed 2 minutes to 72 hours after treatment to determine the temporal range of response by using immunohistochemical staining of the apoptosis marker cleaved caspase-3, phosphorylated gammaH2AX, and HSP70 and of markers of oxidative and nitrative stress (8-hydroxydeoxyguanosine [8-OHdG], 4-hydroxynonenal [4-HNE]-modified proteins, and nitrotyrosine [NT]). Statistical analyses, including t tests and analysis of variance for comparisons where appropriate, were performed.

RESULTS

By 4 hours after RF ablation alone, a 0.48-mm +/- 0.13 (standard deviation) peripheral band with 57.0% +/- 7.3 cleaved caspase-3 positive cells was noted at the ablation margin, whereas a 0.73-mm +/- 0.18 band with 77.7% +/- 6.3 positivity was seen for combination therapy (P < .03 for both comparisons). Combination therapy caused increased and earlier staining for 4-HNE-modified proteins, 8-OHdG, NT, and gammaH2AX with colocalization to cleaved caspase-3 staining. A rim of increased HSP70 was identified peripheral to the area of cleaved caspase-3. Parameters of oxidative and nitrative stress were significantly inhibited by NAC 1 hour following RF ablation, resulting in decreased cleaved caspase-3 positivity (0.28-mm +/- 0.09 band of 25.9% +/- 7.4 positivity vs 0.59-mm +/- 0.11 band of 62.9% +/- 6.0 positivity, P < .001 for both comparisons).

CONCLUSION

Combining RF ablation with liposomal doxorubicin increases cell injury and apoptosis in the zone of increased coagulation by using a mechanism that involves oxidative and nitrative stress that leads to accelerated apoptosis.

摘要

目的

确定在射频 (RF) 消融联合脂质体阿霉素时,氧化和硝化应激和/或细胞凋亡是否会导致凝血增加。

材料和方法

获得动物护理委员会的批准。在费希尔大鼠的 R3230 乳腺腺癌中,分别采用 RF 消融(n = 43)、静脉注射脂质体阿霉素 1 毫克(n = 26)或联合治疗(n = 30)进行治疗,并与对照组(n = 11)进行比较。接受联合治疗的动物亚组(n = 24)在 RF 消融前 24 小时和 1 小时接受 N-乙酰半胱氨酸(NAC)治疗,并分析治疗后 2 分钟至 72 小时的肿瘤,以通过免疫组织化学染色检测凋亡标志物 cleaved caspase-3、磷酸化 γH2AX 和 HSP70 以及氧化和硝化应激标志物(8-羟基脱氧鸟苷 [8-OHdG]、4-羟基壬烯醛 [4-HNE]-修饰蛋白和硝基酪氨酸 [NT])来确定反应的时间范围。进行了统计分析,包括适当情况下的 t 检验和方差分析。

结果

单独进行 RF 消融后 4 小时,消融边缘处可见 0.48 毫米 +/- 0.13(标准差)的外周带,其中 cleaved caspase-3 阳性细胞为 57.0% +/- 7.3%,而联合治疗的带为 0.73 毫米 +/- 0.18,阳性率为 77.7% +/- 6.3%(两者比较均为 P <.03)。联合治疗导致 4-HNE 修饰蛋白、8-OHdG、NT 和 γH2AX 的染色增加和更早出现,并与 cleaved caspase-3 染色共定位。在 cleaved caspase-3 染色区域周围发现 HSP70 增加的边缘。NAC 在 RF 消融后 1 小时显著抑制氧化和硝化应激参数,导致 cleaved caspase-3 阳性率降低(0.28 毫米 +/- 0.09 带为 25.9% +/- 7.4%,0.59 毫米 +/- 0.11 带为 62.9% +/- 6.0%,两者比较均为 P <.001)。

结论

RF 消融联合脂质体阿霉素通过涉及氧化和硝化应激的机制增加凝血增加区域的细胞损伤和细胞凋亡,从而导致细胞凋亡加速。

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