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本文引用的文献

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Tumor necrosis factor alpha and interleukin-6 facilitate corneal lymphangiogenesis in response to herpes simplex virus 1 infection.肿瘤坏死因子α和白细胞介素-6促进角膜淋巴管生成以应对单纯疱疹病毒1感染。
J Virol. 2014 Dec;88(24):14451-7. doi: 10.1128/JVI.01841-14. Epub 2014 Oct 8.
2
Oncolytic reovirus in canine mast cell tumor.溶瘤呼肠孤病毒治疗犬肥大细胞瘤。
PLoS One. 2013 Sep 20;8(9):e73555. doi: 10.1371/journal.pone.0073555. eCollection 2013.
3
Plaque formation by a velogenic Newcastle disease virus in human colorectal cancer cell lines.速发型新城疫病毒在人结肠癌细胞系中形成噬斑。
Acta Virol. 2012;56(4):345-7. doi: 10.4149/av_2012_04_345.
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Tumor targeted adenovirus nanocomplex ionically crosslinked by chitosan.壳聚糖离子交联的肿瘤靶向腺病毒纳米复合物
J Control Release. 2010 Nov 20;148(1):e124. doi: 10.1016/j.jconrel.2010.07.094.
5
Inhibition of the inflammatory cytokine TNF-α increases adenovirus activity in ovarian cancer via modulation of cIAP1/2 expression.抑制炎症细胞因子 TNF-α 通过调节 cIAP1/2 的表达增加卵巢癌细胞中腺病毒的活性。
Mol Ther. 2011 Mar;19(3):490-9. doi: 10.1038/mt.2010.247. Epub 2010 Nov 16.
6
NF-κB targeting by way of IKK inhibition sensitizes lung cancer cells to adenovirus delivery of TRAIL.通过 IKK 抑制靶向 NF-κB 可使肺癌细胞对 TRAIL 腺病毒传递敏感。
BMC Cancer. 2010 Oct 27;10:584. doi: 10.1186/1471-2407-10-584.
7
Systemic administration of a conditionally replicating adenovirus, targeted to angiogenesis, reduced lung metastases burden in cotton rats.对血管生成具有靶向性的条件性复制腺病毒进行全身给药,可减轻棉鼠肺部转移瘤的负担。
Clin Cancer Res. 2009 Mar 1;15(5):1664-73. doi: 10.1158/1078-0432.CCR-08-1670. Epub 2009 Feb 24.
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Treatment of metastatic renal cancer with capsid-modified oncolytic adenoviruses.用衣壳修饰的溶瘤腺病毒治疗转移性肾癌。
Mol Cancer Ther. 2007 Oct;6(10):2728-36. doi: 10.1158/1535-7163.MCT-07-0176.
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Vascular endothelial growth factor promoter-based conditionally replicative adenoviruses for pan-carcinoma application.基于血管内皮生长因子启动子的条件性复制腺病毒在泛癌应用中的研究
Cancer Gene Ther. 2007 Jan;14(1):105-16. doi: 10.1038/sj.cgt.7700991. Epub 2006 Oct 6.
10
A heparan sulfate-targeted conditionally replicative adenovirus, Ad5.pk7-Delta24, for the treatment of advanced breast cancer.一种用于治疗晚期乳腺癌的硫酸乙酰肝素靶向性条件复制腺病毒Ad5.pk7-Delta24。
Gene Ther. 2007 Jan;14(1):58-67. doi: 10.1038/sj.gt.3302830. Epub 2006 Aug 10.

条件性复制腺病毒介导的肿瘤坏死因子对食管癌细胞系和肺癌细胞系的杀伤作用。

Killing effect of TNF-mediated by conditionally replicating adenovirus on esophageal cancer and lung cancer cell lines.

作者信息

Jiang Yue-Quan, Zhang Zhi, Cai Hua-Rong, Zhou Hong

机构信息

Department of Thoracic Surgery, Chongqing Cancer Institute Chongqing, China.

出版信息

Int J Clin Exp Pathol. 2015 Nov 1;8(11):13785-94. eCollection 2015.

PMID:26823692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4713478/
Abstract

OBJECTIVE

The killing effect of TNF mediated by conditionally replicating adenovirus SG502 on human cancer cell lines was assessed by in vivo and in vitro experiments.

METHODS

The recombinant adenovirus SG502-TNF was used to infect human lung cancer cell line A549 and human esophageal cancer cell line TE-1. The expression of the exogenous gene and its inhibitory effect on the tumor cell lines were thus detected. Tumor transplantation experiment was performed in mice with the purpose of assessing the inhibitory effect of the adenovirus on tumor cells and tumor formation. The targeting of the adenovirus and the mechanism of tumor inhibition were discussed by in vivo imaging technology, HE staining and TUNEL assay.

RESULTS

Recombinant adenovirus SG502-TNF targeted the tumor cells specifically with stable expression of TNF, which produced a killing effect on tumor cells by regulating the apoptotic signaling pathway.

CONCLUSION

Recombinant adenovirus SG502-TNF possessed significant killing effect on TE-1 cells either in vivo or in vitro. This finding demonstrated the potential clinical application of adenovirus SG502.

摘要

目的

通过体内和体外实验评估条件复制腺病毒SG502介导的肿瘤坏死因子(TNF)对人癌细胞系的杀伤作用。

方法

用重组腺病毒SG502-TNF感染人肺癌细胞系A549和人食管癌细胞系TE-1。检测外源基因的表达及其对肿瘤细胞系的抑制作用。在小鼠中进行肿瘤移植实验,以评估腺病毒对肿瘤细胞和肿瘤形成的抑制作用。通过体内成像技术、苏木精-伊红(HE)染色和脱氧核糖核苷酸末端转移酶介导的缺口末端标记(TUNEL)法探讨腺病毒的靶向性及肿瘤抑制机制。

结果

重组腺病毒SG502-TNF特异性靶向肿瘤细胞,TNF表达稳定,通过调节凋亡信号通路对肿瘤细胞产生杀伤作用。

结论

重组腺病毒SG502-TNF在体内和体外对TE-1细胞均具有显著的杀伤作用。这一发现证明了腺病毒SG502潜在的临床应用价值。