Publications by authors named "Xiang-Qian Gao"

Circular RNAs (circRNAs) are a distinct class of endogenous RNAs characterized by their covalently closed circular structure. CircRNAs play crucial regulatory roles in various biological processes and pathogenesis. In this study we investigated the role of circRNAs in cardiomyocyte pyroptosis and underlying mechanisms.

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, an important ornamental tree native to East Asia, comprises two subspecies in distinct regions, with wild populations facing suboptimal survival. This study aimed to understand the potential habitat distribution of these subspecies under future climate-change conditions to support climate-adaptive conservation. The maximum entropy (MaxEnt) model was used with occurrence and environmental data to simulate the current and future suitable habitats under various climate scenarios.

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Article Synopsis
  • PIWI-interacting RNAs (piRNAs) play a significant role in cardiovascular diseases, but their involvement in cardiomyocyte death from ischemia/reperfusion (I/R) injury, particularly necroptosis, is not well understood.
  • * A specific piRNA, called heart necroptosis-associated piRNA (HNEAP), has been identified as regulating necroptosis in cardiomyocytes by affecting DNA methylation of Atf7 mRNA through DNMT1.
  • * Elevated levels of HNEAP were found in damaged heart tissue, and inhibiting its action improved heart function, suggesting that targeting the HNEAP-DNMT1-ATF7-CHMP2A pathway could provide new treatments
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Circular RNAs (circRNAs) are differentially expressed in various cardiovascular disease including myocardial ischemia-reperfusion (I/R) injury. However, their functional impact on cardiomyocyte cell death, in particular, in necrotic forms of death remains elusive. In this study, we found that the level of mmu_circ_000338, a cardiac- necroptosis-associated circRNA (CNEACR), was reduced in hypoxia-reoxygenation (H/R) exposed cardiomyocytes and I/R-injured mice hearts.

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Circular RNA (circRNA) has a closed-loop structure, and its 3' and 5' ends are directly covalently connected by reverse splicing, which is more stable than linear RNA. CircRNAs usually possess microRNA (miRNA) binding sites, which can bind miRNAs and inhibit miRNA function. Many studies have shown that circRNAs are involved in the processes of cell senescence, proliferation and apoptosis and a series of signalling pathways, playing an important role in the prevention and treatment of diseases.

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PIWI-interacting RNAs (piRNAs) are recently discovered small non-coding RNAs consisting of 24-35 nucleotides, usually including a characteristic 5-terminal uridine and an adenosine at position 10. PIWI proteins can specifically bind to the unique structure of the 3' end of piRNAs. In the past, it was thought that piRNAs existed only in the reproductive system, but recently, it was reported that piRNAs are also expressed in several other human tissues with tissue specificity.

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Article Synopsis
  • PIWI-interacting RNAs (piRNAs) play a significant role during cardiac hypertrophy, but their specific functions are not fully understood.
  • A newly identified piRNA, named CHAPIR, promotes harmful cardiac growth by interfering with the methylation of Parp10 mRNA, which leads to increased PARP10 expression.
  • Targeting the CHAPIR-METTL3-PARP10-NFATC4 signaling pathway could offer new therapeutic strategies for managing cardiac hypertrophy and related heart issues.
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PH domain leucine-rich repeat protein phosphatase 2 (PHLPP2) belongs to the phosphokinase family, that has been reported to play an important role in several cancers. However, the expression of PHLPP2 and its correlation with clinicopathologic characteristics in colorectal cancer (CRC) have yet to be determined. The aim of this study is to investigate the expression of PHLPP2 and explore its role in CRC.

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Mitochondrial dysfunction is involved in the pathogenesis of various cardiovascular disorders. Although mitochondrial dynamics, including changes in mitochondrial fission and fusion, have been implicated in the development of cardiac hypertrophy, the underlying molecular mechanisms remain mostly unknown. Here, we show that NFATc3, miR-153-3p, and mitofusion-1 (Mfn1) constitute a signaling axis that mediates mitochondrial fragmentation and cardiomyocyte hypertrophy.

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