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组蛋白去乙酰化酶抑制剂对cathelicidin和防御素的调节作用:多药耐药性传染病的潜在治疗方法。

Modulation of cathelicidin and defensins by histone deacetylase inhibitors: A potential treatment for multi-drug resistant infectious diseases.

作者信息

Rodríguez-Carlos Adrián, Jacobo-Delgado Yolanda M, Santos-Mena Alan O, Rivas-Santiago Bruno

机构信息

Medical Research Unit-Zacatecas, Mexican Institute for Social Security-IMSS, Zacatecas, Mexico.

Medical Research Unit-Zacatecas, Mexican Institute for Social Security-IMSS, Zacatecas, Mexico.

出版信息

Peptides. 2021 Jun;140:170527. doi: 10.1016/j.peptides.2021.170527. Epub 2021 Mar 17.

Abstract

Infectious diseases are an important growing public health problem, which perspective has worsened due to the increasing number of drug-resistant strains in the last few years. Although diverse solutions have been proposed, one viable solution could be the use of immune system modulators. The induction of the immune response can be increased by histone deacetylase inhibitors (iHDAC), which in turn modulate the chromatin and increase the activation of different cellular pathways and nuclear factors such as STAT3, HIF-1α NF-kB, C/EBPα and, AP-1. These pathways are capable to promote several immune response-related molecules including those with antimicrobial properties such as antimicrobial peptides (AMPs) that lead to the elimination of pathogens including multi drug-resistant strains.

摘要

传染病是一个日益严重的重要公共卫生问题,由于过去几年耐药菌株数量的增加,这一问题的前景更加恶化。尽管已经提出了多种解决方案,但一个可行的办法可能是使用免疫系统调节剂。组蛋白脱乙酰酶抑制剂(iHDAC)可增强免疫反应的诱导,进而调节染色质并增强不同细胞途径和核因子(如STAT3、HIF-1α、NF-κB、C/EBPα和AP-1)的激活。这些途径能够促进多种与免疫反应相关的分子,包括具有抗菌特性的分子,如抗菌肽(AMP),从而导致包括多重耐药菌株在内的病原体被清除。

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