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Therapeutic improvement of a stroma-targeted CRAd by incorporating motives responsive to the melanoma microenvironment.通过纳入对黑色素瘤微环境有响应的动机,来改善基质靶向的 CRAd 的治疗效果。
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A dual-regulated oncolytic adenovirus expressing interleukin-24 sensitizes melanoma cells to temozolomide via the induction of apoptosis.一种表达白细胞介素-24的双调控溶瘤腺病毒通过诱导凋亡使黑色素瘤细胞对替莫唑胺敏感。
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本文引用的文献

1
Combining conditionally replicating adenovirus-mediated gene therapy with chemotherapy: a novel antitumor approach.联合条件复制型腺病毒介导的基因治疗与化疗:一种新型抗肿瘤方法。
Int J Cancer. 2011 Jul 15;129(2):263-74. doi: 10.1002/ijc.25948. Epub 2011 Apr 20.
2
Enhanced anti-tumor activity by the combination of a conditionally replicating adenovirus mediated interleukin-24 and dacarbazine against melanoma cells via induction of apoptosis.条件复制型腺病毒介导白细胞介素-24 联合达卡巴嗪增强对黑色素瘤细胞的抗肿瘤活性,通过诱导细胞凋亡。
Cancer Lett. 2010 Aug 28;294(2):220-8. doi: 10.1016/j.canlet.2010.02.003. Epub 2010 Feb 26.
3
Targeted radiotherapy for prostate cancer with an oncolytic adenovirus coding for human sodium iodide symporter.使用编码人钠碘同向转运体的溶瘤腺病毒对前列腺癌进行靶向放疗。
Clin Cancer Res. 2009 Sep 1;15(17):5396-403. doi: 10.1158/1078-0432.CCR-08-2571. Epub 2009 Aug 25.
4
Double E1B 19 kDa- and E1B 55 kDa-deleted oncolytic adenovirus in combination with radiotherapy elicits an enhanced anti-tumor effect.双 E1B 19 kDa 和 E1B 55 kDa 缺失的溶瘤腺病毒联合放射治疗可增强抗肿瘤作用。
Gene Ther. 2009 Sep;16(9):1111-21. doi: 10.1038/gt.2009.72. Epub 2009 Jun 4.
5
Historical perspective and recent insights into our understanding of the molecular and biochemical basis of the antitumor properties of mda-7/IL-24.关于我们对mda-7/IL-24抗肿瘤特性的分子和生化基础理解的历史视角与近期见解。
Cancer Biol Ther. 2009 Mar;8(5):391-400. doi: 10.4161/cbt.8.5.7581. Epub 2009 Mar 8.
6
Armed replicating adenoviruses for cancer virotherapy.用于癌症病毒疗法的武装复制腺病毒
Cancer Gene Ther. 2009 Jun;16(6):473-88. doi: 10.1038/cgt.2009.3. Epub 2009 Feb 6.
7
IFN-alpha and bortezomib overcome Bcl-2 and Mcl-1 overexpression in melanoma cells by stimulating the extrinsic pathway of apoptosis.干扰素-α和硼替佐米通过刺激凋亡的外源性途径,克服黑色素瘤细胞中Bcl-2和Mcl-1的过表达。
Cancer Res. 2008 Oct 15;68(20):8351-60. doi: 10.1158/0008-5472.CAN-08-0426.
8
Ad-MDA-7; INGN 241: a review of preclinical and clinical experience.腺病毒介导的 MDA-7;INGN 241:临床前和临床经验综述。
Expert Opin Biol Ther. 2008 Oct;8(10):1633-43. doi: 10.1517/14712598.8.10.1633.
9
MDA-7/IL-24 plus radiation enhance survival in animals with intracranial primary human GBM tumors.黑色素瘤分化相关基因7/白细胞介素-24联合放疗可提高患有颅内原发性人类胶质母细胞瘤的动物的生存率。
Cancer Biol Ther. 2008 Jun;7(6):917-33. doi: 10.4161/cbt.7.6.5928. Epub 2008 Mar 19.
10
Apoptosis pathways and oncolytic adenoviral vectors: promising targets and tools to overcome therapy resistance of malignant melanoma.凋亡途径与溶瘤腺病毒载体:克服恶性黑色素瘤治疗耐药性的有前景的靶点和工具。
Exp Dermatol. 2008 Jan;17(1):1-11. doi: 10.1111/j.1600-0625.2007.00655.x.

携带白细胞介素-24 的条件复制腺病毒通过细胞凋亡使黑色素瘤细胞对放射治疗敏感。

A conditionally replicating adenovirus carrying interleukin-24 sensitizes melanoma cells to radiotherapy via apoptosis.

机构信息

Department of Dermatology, Affiliated Hospital of Xuzhou Medical College, Xuzhou 221002, China.

出版信息

Mol Oncol. 2012 Aug;6(4):383-91. doi: 10.1016/j.molonc.2012.05.001. Epub 2012 May 18.

DOI:10.1016/j.molonc.2012.05.001
PMID:22673233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5528358/
Abstract

Combinatorial therapy is the current trend of the development of novel cancer treatments due to the high heterogenous nature of solid tumors. In this study, we investigated the effects of the combined use of a conditionally replicating adenovirus carrying IL-24 (ZD55-IL-24) and radiotherapy on the proliferation and apoptosis of melanoma A375 cells in vitro and in vivo. Compared with either agent used alone, ZD55-IL-24 combined with radiotherapy significantly inhibited cell proliferation, accompanied with increased apoptosis. Radiotherapy did not affect the expression of IL-24 and E1A of ZD55-IL-24-treated cells, but increased the expression of Bax, promoted the activation of caspase-3, while decreasing Bcl-2 levels. Thus, this synergistic effect of ZD55-IL-24 in combination with radiotherapy provides a novel strategy for the development of melanoma therapies, and is a promising approach for further clinical development.

摘要

联合治疗是新型癌症治疗发展的当前趋势,这是由于实体瘤具有高度异质性。在这项研究中,我们研究了携带 IL-24 的条件复制腺病毒(ZD55-IL-24)与放射疗法联合使用对体外和体内黑色素瘤 A375 细胞增殖和凋亡的影响。与单独使用任一药物相比,ZD55-IL-24 联合放射疗法可显著抑制细胞增殖,并伴有细胞凋亡增加。放射疗法不影响 ZD55-IL-24 处理的细胞中 IL-24 和 E1A 的表达,但会增加 Bax 的表达,促进 caspase-3 的激活,同时降低 Bcl-2 水平。因此,ZD55-IL-24 联合放射疗法的这种协同作用为黑色素瘤治疗的发展提供了一种新策略,是进一步临床开发的有前途的方法。