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首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Irradiated human endothelial progenitor cells induce bystander killing in human non-small cell lung and pancreatic cancer cells
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Irradiated human endothelial progenitor cells induce bystander killing in human non-small cell lung and pancreatic cancer cells

机译:辐射的人内皮祖细胞在人非小细胞肺癌和胰腺癌细胞中诱导旁观者杀伤

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摘要

Purpose To investigate whether irradiated human endothelial progenitor cells (hEPC) could induce bystander killing in the A549 non-small cell lung cancer (NSCLC) cells and help explain the improved radiation-induced tumor cures observed in A549 tumor xenografts co-injected with hEPC.Materials and methods We investigated whether co-injection of CBM3 hEPC with A549 NSCLC cells would alter tumor xenograft growth rate or tumor cure after a single dose of 0 or 5Gy of X-rays. We then utilized dual chamber Transwell dishes, to test whether medium from irradiated CBM3 and CBM4 hEPC would induce bystander cell killing in A549 cells, and as an additional control, in human pancreatic cancer MIA PaCa-2 cells. The CBM3 and CBM4 hEPC were plated into the upper Transwell chamber and the A549 or MIA PaCa-2 cells were plated in the lower Transwell chamber. The top inserts with the CBM3 or CBM4 hEPC cells were subsequently removed, irradiated, and then placed back into the Transwell dish for 3h to allow for diffusion of any potential bystander factors from the irradiated hEPC in the upper chamber through the permeable membrane to the unirradiated cancer cells in the lower chamber. After the 3h incubation, the cancer cells were re-plated for clonogenic survival.Results We found that co-injection of CBM3 hEPC with A549 NSCLC cells significantly increased the tumor growth rate compared to A549 cells alone, but paradoxically also increased A549 tumor cure after a single dose of 5Gy of X-rays (p<0.05). We hypothesized that irradiated hEPC may be inducing bystander killing in the A549 NSCLC cells in tumor xenografts, thus improving tumor cure. Bystander studies clearly showed that exposure to the medium from irradiated CBM3 and CBM4 hEPC induced significant bystander killing and decreased the surviving fraction of A549 and MIA PaCa-2 cells to 0.46 (46%)0.22 and 0.74 +/- 0.07 (74%) respectively (p<0.005, p<0.0001). In addition, antibody depletion studies demonstrated that the bystander killing induced in both A549 and MIA PaCa-2 cells was mediated by the cytokines TNF- and TGF- (p<0.05).Conclusions These data provide evidence that irradiated hEPC can induce strong bystander killing in A549 and MIA PaCa-2 human cancer cells and that this bystander killing is mediated by the cytokines TNF- and TGF-beta.
机译:目的探讨经辐射的人内皮祖细胞(hEPC)是否可以诱导旁观者在A549非小细胞肺癌(NSCLC)细胞中的杀伤,并帮助解释在与hEPC共注射的A549异种移植物中观察到的放射诱导的肿瘤治愈方法得到改善。材料和方法我们研究了将CBM3 hEPC与A549 NSCLC细胞一起注射是否会在单剂量0或5Gy的X射线照射后改变肿瘤异种移植物的生长速率或治愈肿瘤。然后,我们使用双室Transwell皿,测试来自辐射的CBM3和CBM4 hEPC的培养基是否会诱导人胰腺癌MIA PaCa-2细胞中A549细胞中的旁观者细胞杀伤,并作为另外的对照。将CBM3和CBM4 hEPC接种到上部Transwell室中,将A549或MIA PaCa-2细胞接种到下部Transwell室中。随后将带有CBM3或CBM4 hEPC细胞的顶部插入物取出,进行辐照,然后放回Transwell皿中3h,以允许任何潜在的旁观者因素从上腔室中辐照过的hEPC穿过可渗透膜扩散到未辐照下腔室中有癌细胞。孵育3h后,将癌细胞重新铺平板以保持克隆形成的存活。结果我们发现,与单独使用A549细胞相比,将CBM3 hEPC与A549 NSCLC细胞同时注射显着提高了肿瘤的生长速度,但自相矛盾的是,在术后A549肿瘤治愈率也提高了一次5Gy的X射线剂量(p <0.05)。我们假设辐射的hEPC可能在异种移植物中的A549 NSCLC细胞中诱导旁观者杀伤,从而改善了肿瘤的治愈。旁观者研究清楚地表明,暴露于经辐照的CBM3和CBM4 hEPC的培养基可引起显着的旁观者杀死,并将A549和MIA PaCa-2细胞的存活率分别降低至0.46(46%)0.22和0.74 +/- 0.07(74%) (p <0.005,p <0.0001)。此外,抗体耗竭研究表明,A549和MIA PaCa-2细胞诱导的旁观者杀伤是由细胞因子TNF-和TGF-介导的(p <0.05)。结论这些数据提供了证据,证明辐射的hEPC可以诱导强烈的旁观者杀伤。在A549和MIA PaCa-2人类癌细胞中,这种旁观者的杀死是由细胞因子TNF-和TGF-β介导的。

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