基于机器学习揭示ANXA6作为子痫前期自噬相关的新靶点

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Baoping Zhu, Huizhen Geng, Fan Yang, Yanxin Wu, Tiefeng Cao, Dongyu Wang, Zilian Wang
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引用次数: 0

摘要

子痫前期(PE)是一种与自噬相关的严重妊娠并发症。本研究试图通过生物信息学和机器学习来揭示子痫前期自噬相关基因。对GEO系列中的GSE75010进行WGCNA鉴定PE中的关键模块基因。从THANATOS中提取的自噬基因与模块基因重叠产生pe相关的自噬基因。此外,关键步骤涉及使用两种机器学习算法(LASSO和SVM-RFE)进行降维。通过定量逆转录聚合酶链反应、免疫印迹和免疫组织化学进一步验证候选基因。我们在HTR-8/SVneo细胞系上进行了初步实验,探讨候选基因在自噬调控中的作用。WGCNA从5个枢纽中鉴定出291个基因,与THANATOS获得的1087个自噬相关基因重叠后,鉴定出42个pe相关ARGs。通过SVM-RFE和LASSO分析,ANXA6被认为是潜在的靶点。在胎盘样品中验证了ANXA6 mRNA和蛋白的表达。在HTR8/SVneo细胞中,调节ANXA6表达可改变自噬水平。抑制ANXA6可产生抗自噬作用,这一作用可通过CAL101 (PI3K、Akt和mTOR的抑制剂)治疗逆转。我们观察到ANXA6可能是PE的一个可能的作用靶点,并且自噬可能对PE的发病机制至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Revealing ANXA6 as a Novel Autophagy-related Target for Pre-eclampsia Based on the Machine Learning
Preeclampsia (PE) is a severe pregnancy complication associated with autophagy. This research sought to uncover autophagy-related genes in pre-eclampsia through bioinformatics and machine learning. GSE75010 from the GEO series was subjected to WGCNA to identify key modular genes in PE. Autophagy genes retrieved from the THANATOS overlapped with the modular genes to yield PE-related autophagy genes. Furthermore, the crucial step involved the utilization of two machine learning algorithms (LASSO and SVM-RFE) for dimensionality reduction. The candidate gene was further verified by quantitative reverse transcription polymerase chain reaction, western blot, and immunohistochemistry. Preliminary experiments were conducted on HTR-8/SVneo cell lines to explore the role of candidate genes in autophagy regulation. WGCNA identified 291 genes from 5 hubs, and after overlapping with 1087 autophagy-related genes obtained from THANATOS, 42 PE-related ARGs were identified. ANXA6 was recognized as a potential target through SVM-RFE and LASSO analyses. The mRNA and protein expression of ANXA6 were verified in placenta samples. In HTR8/SVneo cells, modulating ANXA6 expression altered autophagy levels. Knocking down ANXA6 resulted in an anti-autophagy effect, which was reversed by treatment with CAL101, an inhibitor of PI3K, Akt, and mTOR. We observed that ANXA6 may serve as a possible PE action target and that autophagy may be crucial to the pathogenesis of PE.
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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