Xiaoqian Liu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Xiaoqian Liu has a total of 15 co-authors. Here are the top co-authors by number of shared publications:
Guangcan Shao
National Institute of Biological Sciences, Beijing 102206, China
2 shared publications- Jing Li
Beijing Key Laboratory of DNA Damage Response and College of Life Sciences, Capital Normal University, Beijing 100048, China
2 shared publications Meng-Qiu Dong
National Institute of Biological Sciences, Beijing 102206, China
2 shared publicationsAiyun Yuan
Beijing Key Laboratory of DNA Damage Response and College of Life Sciences, Capital Normal University, Beijing 100048, China
1 shared publicationJianxin Zhao
Beijing Key Laboratory of DNA Damage Response and College of Life Sciences, Capital Normal University, Beijing, China
1 shared publication- Jiaxian Song
State Key Laboratory of Microbial Technology, Shandong University, Qingdao 266237, China
1 shared publication
Latest Publications
- Open Access
- 1 June 2025
- Published by Tsinghua University Press in Oral Science and Homeostatic Medicine
- Vol. 1 (1)
Gut microbiota dysbiosis: the hidden roles in human aging and age-related diseases
Emerging evidence has illuminated the critical role of gut microbiota in regulating health and longevity. In this review, we systematically summarize the changes in gut microbiota associated with aging and age-related diseases, including gastrointestinal tract diseases, neurodegenerative disorders, and metabolic dysfunction syndromes. We will also explore the underlying mechanisms, particularly those related to metabolic and immune pathways, highlighting a feedback loop model of "microbial dysbiosis-metabolic dysfunction-chronic inflammation". Furthermore, current interventions related to gut microbiota, including dietary strategies, fecal microbiota transplantation, prebiotics, probiotics, and phage therapies, will be discussed. We will also explore cutting-edge technologies such as artificial intelligence (AI)-driven microbiome analysis, microbial engineering, and organ-on-chip systems, as well as the challenges that remain in this field. Overall, this review provides a theoretical framework and directional guidance for rejuvenating aging and age-related diseases via targeting the gut microbiota.
- 1 June 2025
- Published by Tsinghua University Press in Oral Science and Homeostatic Medicine
- Vol. 1 (1)
Open AccessGut microbiota dysbiosis: the hidden roles in human aging and age-related diseases
Emerging evidence has illuminated the critical role of gut microbiota in regulating health and longevity. In this review, we systematically summarize the changes in gut microbiota associated with aging and age-related diseases, including gastrointestinal tract diseases, neurodegenerative disorders, and metabolic dysfunction syndromes. We will also explore the underlying mechanisms, particularly those related to metabolic and immune pathways, highlighting a feedback loop model of "microbial dysbiosis-metabolic dysfunction-chronic inflammation". Furthermore, current interventions related to gut microbiota, including dietary strategies, fecal microbiota transplantation, prebiotics, probiotics, and phage therapies, will be discussed. We will also explore cutting-edge technologies such as artificial intelligence (AI)-driven microbiome analysis, microbial engineering, and organ-on-chip systems, as well as the challenges that remain in this field. Overall, this review provides a theoretical framework and directional guidance for rejuvenating aging and age-related diseases via targeting the gut microbiota.
- Open Access
- 29 May 2025
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 301 (7) , 110314
SUMOylation targets O-GlcNAcase to chaperone-mediated autophagy
- 29 May 2025
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 301 (7) , 110314
Open AccessSUMOylation targets O-GlcNAcase to chaperone-mediated autophagy
- Open Access
Bidirectional Interplay Among Non-Coding RNAs, the Microbiome, and the Host During Development and Diseases
It is widely known that the dysregulation of non-coding RNAs (ncRNAs) and dysbiosis of the gut microbiome play significant roles in host development and the progression of various diseases. Emerging evidence has highlighted the bidirectional interplay between ncRNAs and the gut microbiome. This article aims to review the current understanding of the molecular mechanisms underlying the crosstalk between ncRNAs, especially microRNA (miRNA), and the gut microbiome in the context of development and diseases, such as colorectal cancer, inflammatory bowel diseases, neurological disorders, obesity, and cardiovascular disease. Ultimately, this review seeks to provide a foundation for exploring the potential roles of ncRNAs and gut microbiome interactions as biomarkers and therapeutic targets for clinical diagnosis and treatment, such as ncRNA mimics, antisense oligonucleotides, and small-molecule compounds, as well as probiotics, prebiotics, and diets.
Open AccessBidirectional Interplay Among Non-Coding RNAs, the Microbiome, and the Host During Development and Diseases
It is widely known that the dysregulation of non-coding RNAs (ncRNAs) and dysbiosis of the gut microbiome play significant roles in host development and the progression of various diseases. Emerging evidence has highlighted the bidirectional interplay between ncRNAs and the gut microbiome. This article aims to review the current understanding of the molecular mechanisms underlying the crosstalk between ncRNAs, especially microRNA (miRNA), and the gut microbiome in the context of development and diseases, such as colorectal cancer, inflammatory bowel diseases, neurological disorders, obesity, and cardiovascular disease. Ultimately, this review seeks to provide a foundation for exploring the potential roles of ncRNAs and gut microbiome interactions as biomarkers and therapeutic targets for clinical diagnosis and treatment, such as ncRNA mimics, antisense oligonucleotides, and small-molecule compounds, as well as probiotics, prebiotics, and diets.
- Open Access
- 2 November 2024
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 300 (12) , 107956
O-GlcNAcylation of RPA2 at S4/S8 antagonizes phosphorylation and regulates checkpoint activation during replication stress
- 2 November 2024
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 300 (12) , 107956
Open AccessO-GlcNAcylation of RPA2 at S4/S8 antagonizes phosphorylation and regulates checkpoint activation during replication stress