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基于人类和蝾螈在伤口愈合过程中基因表达的比较进行癌症药物再定位。

Cancer Drug Repositioning by Comparison of Gene Expression in Humans and Axolotl () During Wound Healing.

机构信息

1Department of Genetics and Bioengineering, Istanbul Okan University, Istanbul, Turkey.

2Department of Bioengineering, Marmara University, Istanbul, Turkey.

出版信息

OMICS. 2019 Aug;23(8):389-405. doi: 10.1089/omi.2019.0093. Epub 2019 Jul 15.

Abstract

Urodele amphibians such as the axolotl () display a large capacity for tissue regeneration and remarkable resistance to cancer. As a model organism, axolotl thus offers a unique opportunity for cancer research and anticancer drug discovery, not to mention the discerning mechanisms that underpin controlled cellular growth and regeneration versus cancer. To the best of our knowledge, little is known on comparative gene expression changes during regeneration events such as wound healing in axolotl and humans. Using publicly available transcriptomics data and bioinformatics analyses, we examined the differential gene expression signatures in skin wound samples from axolotl and humans after skin biopsy punch injury, in comparison with intact (uninjured) control skin samples. We identified 95 genes exhibiting a reversal expression pattern between humans and axolotl during the wound healing/regeneration period. These genes were significantly associated with collagen biosynthesis, extracellular matrix organization, PI3K-Akt signaling pathway, immune system response, and apoptotic process. Furthermore, this new gene set exhibited high prognostic performance in discriminating the survival risk in skin-related cancers, including melanoma (hazard ratio [HR] = 8.14,  < 10), oral cancer (HR >100,  < 10), and head and neck carcinoma (HR = 5.29,  < 10). Moreover, considering these gene signatures, we repositioned 11 small molecules as potential anticancer drug candidates indicating reversal effects on upregulated human genes and downregulated axolotl genes or mimicking downregulated human genes and upregulated axolotl genes. We anticipate that this study offers new insights on gene signatures bridging regeneration mechanisms with tumorigenesis and cancer drug repositioning.

摘要

蝾螈等有尾两栖动物表现出很强的组织再生能力和对癌症的显著抵抗力。作为一种模式生物,蝾螈为癌症研究和抗癌药物发现提供了独特的机会,更不用说那些控制细胞有丝分裂和再生与癌症的辨别机制了。据我们所知,对于蝾螈和人类在伤口愈合等再生事件中比较基因表达变化知之甚少。利用公开的转录组学数据和生物信息学分析,我们比较了蝾螈和人类皮肤活检穿刺损伤后皮肤伤口样本与完整(未受伤)对照皮肤样本中的差异基因表达特征。我们鉴定出了 95 个在人类和蝾螈的伤口愈合/再生期间表现出逆转表达模式的基因。这些基因与胶原蛋白生物合成、细胞外基质组织、PI3K-Akt 信号通路、免疫系统反应和细胞凋亡过程显著相关。此外,这个新的基因集在区分皮肤相关癌症(包括黑色素瘤[HR=8.14,<10]、口腔癌[HR>100,<10]和头颈部癌[HR=5.29,<10])的生存风险方面表现出了很高的预后性能。此外,考虑到这些基因特征,我们将 11 种小分子重新定位为有潜力的抗癌药物候选物,这些小分子对上调的人类基因具有逆转作用,对下调的蝾螈基因具有上调作用,或者模拟下调的人类基因和上调的蝾螈基因。我们预计,这项研究将为连接再生机制与肿瘤发生和癌症药物再定位的基因特征提供新的见解。

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