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瘤周给予粒细胞集落刺激因子诱导鼠乳腺腺癌细胞发生凋亡反应。

Peritumoral administration of granulocyte colony-stimulating factor induces an apoptotic response on a murine mammary adenocarcinoma.

机构信息

Instituto de Química y Fisicoquímica Biológicas (UBA-CONICET), Facultad de Farmacia y Bioquímica, Buenos Aires, Argentina.

出版信息

Cancer Biol Ther. 2009 Sep;8(18):1737-43. doi: 10.4161/cbt.8.18.9210. Epub 2009 Sep 6.

Abstract

The aim of the present study was to evaluate the in vivo effect of granulocyte colony-stimulating factor (G-CSF) on LM3 murine mammary adenocarcinoma cells subcutaneously implanted in Balb/c mice as experimental models. We showed that the peritumoral administration of 100 microg/kg of G-CSF diminished tumor progression, while no cytokine effect on LM3 cell proliferation was observed in vitro. Histological examination of G-CSF-treated tumors revealed infiltration of neutrophils and mononuclear cells. Apoptotic cells were identified by TUNEL assays. Western blot analysis of tumor lysates showed that G-CSF treatment increased the amount of Fas-L, TRAIL and Bax proteins, whereas decreased the expression of procaspase 3 and Bcl-2. In addition, cytokine arrays showed an increment in the amount of IL-12, IL-13 and TNFalpha. Our results suggest that the presence of G-CSF within tumor microenvironment would induce an immune response which eliminates tumor cells by apoptosis. Both death receptor and mitochondrial pathways would be involved in LM3 tumor cell death. We believe that the final local G-CSF concentration at the tumor site and each particular type of tumor should be carefully taken into account in order to evaluate the effect of the cytokine on tumor progression.

摘要

本研究旨在评估粒细胞集落刺激因子(G-CSF)对皮下植入 Balb/c 小鼠的 LM3 鼠乳腺腺癌细胞的体内作用,作为实验模型。我们发现,肿瘤周围给予 100μg/kg 的 G-CSF 可抑制肿瘤进展,而体外实验未观察到 G-CSF 对 LM3 细胞增殖的细胞因子作用。G-CSF 治疗肿瘤的组织学检查显示中性粒细胞和单核细胞浸润。TUNEL 检测鉴定凋亡细胞。肿瘤裂解物的 Western blot 分析表明,G-CSF 处理增加 Fas-L、TRAIL 和 Bax 蛋白的量,而降低 procaspase 3 和 Bcl-2 的表达。此外,细胞因子阵列显示 IL-12、IL-13 和 TNFalpha 的量增加。我们的结果表明,肿瘤微环境中 G-CSF 的存在会诱导免疫反应,通过细胞凋亡消除肿瘤细胞。死亡受体和线粒体途径都可能参与 LM3 肿瘤细胞的死亡。我们认为,为了评估细胞因子对肿瘤进展的影响,应仔细考虑肿瘤部位的最终局部 G-CSF 浓度和每种特定类型的肿瘤。

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