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Oncolytic adenovirus encoding tumor necrosis factor-related apoptosis inducing ligand (TRAIL) inhibits the growth and metastasis of triple-negative breast cancer

机译:编码肿瘤坏死因子相关凋亡诱导配体(TRAIL)的溶瘤腺病毒抑制三阴性乳腺癌的生长和转移

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Tumor necrosis factor-related apoptosis inducing ligand (TRAIL) is a promising cancer therapeutic target due to its selective apoptosis-inducing effect in cancer cells. To efficiently deliver TRAIL to the tumor cells, an oncolytic adenovirus (p55-hTERT-HRE-TRAIL) carrying the TRAIL coding sequence was constructed. In the present study, we aimed to investigate the effect of p55-hTERT-HRE-TRAIL on the growth and metastasis of triple-negative breast cancer (TNBC). We observed that infection of the recombinant adenovirus resulted in expression of TRAIL and massive cell death in a TNBC cell line MDA-MB-231. This effect is much weaker in MCF-10A, which is a normal breast cell line. Administration of P55- HTERT-HRE-TRAIL significantly reduced orthotopic breast tumor growth and extended survival in a metastatic model. Our results suggest the oncolytic adenovirus armed with P55-HTERT-HRE-TRAIL, which exhibited enhanced anti-tumor activity and improved survival, is a promising candidate for virotherapy of TNBC.
机译:肿瘤坏死因子相关的凋亡诱导配体(TRAIL)由于其在癌细胞中的选择性凋亡诱导作用而成为有希望的癌症治疗靶标。为了有效地将TRAIL递送至肿瘤细胞,构建了携带TRAIL编码序列的溶瘤腺病毒(p55-hTERT-HRE-TRAIL)。在本研究中,我们旨在研究p55-hTERT-HRE-TRAIL对三阴性乳腺癌(TNBC)生长和转移的影响。我们观察到重组腺病毒的感染导致TNBC细胞系MDA-MB-231中TRAIL的表达和大量细胞死亡。在正常乳腺细胞系MCF-10A中,这种作用要弱得多。在转移模型中,P55-HTERT-HRE-TRAIL的使用可显着降低原位乳腺肿瘤的生长并延长生存期。我们的结果表明,装备有P55-HTERT-HRE-TRAIL的溶瘤腺病毒具有增强的抗肿瘤活性和改善的存活率,是TNBC病毒治疗的有希望的候选者。

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