Yuying Liu

ORCID: 0000-0003-2182-7210
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About
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Research Areas
  • Cancer, Hypoxia, and Metabolism
  • Cancer-related molecular mechanisms research
  • RNA modifications and cancer
  • Immune cells in cancer
  • Circular RNAs in diseases
  • Extracellular vesicles in disease
  • Cellular Mechanics and Interactions
  • Immune Cell Function and Interaction
  • RNA Research and Splicing
  • COVID-19 Clinical Research Studies
  • Epigenetics and DNA Methylation
  • Cancer Cells and Metastasis
  • Diet and metabolism studies
  • CAR-T cell therapy research
  • Mitochondrial Function and Pathology
  • Cancer Immunotherapy and Biomarkers
  • Inflammasome and immune disorders
  • Pancreatic function and diabetes
  • Luminescence and Fluorescent Materials
  • Caveolin-1 and cellular processes
  • Immunotherapy and Immune Responses
  • Traditional Chinese Medicine Analysis
  • Cancer-related gene regulation
  • SARS-CoV-2 and COVID-19 Research
  • Molecular Sensors and Ion Detection

Xuzhou Medical College
2022-2025

Hebei University of Technology
2023-2025

Sun Yat-sen University Cancer Center
2019-2025

State Key Laboratory of Oncology in South China
2020-2025

Sun Yat-sen University
2019-2025

Shanghai Jiao Tong University
2017-2025

Renji Hospital
2025

Peking University
2008-2024

Peking University Third Hospital
2024

Beihang University
2005-2024

Cytokine release syndrome (CRS) counteracts the effectiveness of chimeric antigen receptor (CAR) T cell therapy in cancer patients, but mechanism underlying CRS remains unclear. Here, we show that tumor pyroptosis triggers during CAR therapy. We find cells rapidly activate caspase 3 target through granzyme B. The latter cleaves gasdermin E (GSDME), a pore-forming protein highly expressed B leukemic and other cells, which results extensive pyroptosis. Consequently, pyroptosis-released factors...

10.1126/sciimmunol.aax7969 article EN Science Immunology 2020-01-03

Abstract Resetting tumor-associated macrophages (TAMs) is a promising strategy to ameliorate the immunosuppressive tumor microenvironment and improve innate adaptive antitumor immunity. Here we show that chloroquine (CQ), proven anti-malarial drug, can function as an immune modulator switches TAMs from M2 tumor-killing M1 phenotype. Mechanistically, CQ increases macrophage lysosomal pH, causing Ca 2+ release via channel mucolipin-1 (Mcoln1), which induces activation of p38 NF-κB, thus...

10.1038/s41467-018-03225-9 article EN cc-by Nature Communications 2018-02-22

Interactions with the immune system may lead tumorigenic cells into dormancy. However, underlying molecular mechanism is poorly understood. Using a 3D fibrin gel model, we show that IFN-γ induces tumour-repopulating (TRCs) to enter dormancy through an indolamine 2,3-dioxygenase 1 (IDO1)-kynurenine (Kyn)-aryl hydrocarbon receptor (AhR)-p27 dependent pathway. Mechanistically, signalling triggers differentiated tumour cell apoptosis via STAT1; however, when IDO1 and AhR are highly expressed as...

10.1038/ncomms15207 article EN cc-by Nature Communications 2017-05-10

Abstract The existence of breast cancer stem cells (BCSCs) is a major reason underlying metastasis and recurrence after chemotherapy radiotherapy. Targeting BCSCs may ameliorate relapse therapy resistance. Here we report that expression the pseudokinase Tribble 3 (TRIB3) positively associates with stemness progression. Elevated TRIB3 supports by interacting AKT to interfere FOXO1-AKT interaction suppress FOXO1 phosphorylation, ubiquitination, degradation E3 ligases SKP2 NEDD4L. accumulated...

10.1038/s41467-019-13700-6 article EN cc-by Nature Communications 2019-12-16

Abstract Our current understanding of how sugar metabolism affects inflammatory pathways in macrophages is incomplete. Here, we show that glycogen an important event controls macrophage-mediated responses. IFN-γ/LPS treatment stimulates to synthesize glycogen, which then channeled through glycogenolysis generate G6P and further the pentose phosphate pathway yield abundant NADPH, ensuring high levels reduced glutathione for macrophage survival. Meanwhile, also increases UDPG receptor P2Y 14...

10.1038/s41467-020-15636-8 article EN cc-by Nature Communications 2020-04-14

Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) invades the alveoli, where abundant alveolar macrophages (AMs) reside. How AMs respond to SARS-CoV-2 invasion remains elusive. Here, we show that classically activated M1 facilitate viral spread; however, alternatively M2 limit spread. utilize cellular softness efficiently take up SARS-CoV-2. Subsequently, invaded viruses over endo-lysosomal system escape. have a lower endosomal pH, favoring membrane fusion and allowing...

10.1038/s41421-021-00258-1 article EN cc-by Cell Discovery 2021-04-13

Background Colorectal cancer (CRC) is among the most common malignant cancers worldwide, and its development influenced by inflammation, nutrition, immune status. Therefore, we combined C-reactive protein (CRP), albumin, lymphocyte, which could reflect above status, to be CRP-albumin-lymphocyte (CALLY) index, evaluated association with overall survival (OS) in patients CRC. Methods The clinicopathological laboratory characteristics of 1260 CRC were collected from Investigation on Nutrition...

10.3389/fimmu.2023.1131496 article EN cc-by Frontiers in Immunology 2023-03-30

Silent hypoxia has emerged as a unique feature of coronavirus disease 2019 (COVID-19). In this study, we show that mucins are accumulated in the bronchoalveolar lavage fluid (BALF) COVID-19 patients and upregulated lungs severe respiratory syndrome 2 (SARS-CoV-2)-infected mice macaques. We find induction either interferon (IFN)-β or IFN-γ upon SARS-CoV-2 infection results activation aryl hydrocarbon receptor (AhR) signaling through an IDO-Kyn-dependent pathway, leading to transcriptional...

10.1038/s41422-020-00435-z article EN cc-by Cell Research 2020-11-06

Article4 December 2020Open Access Source DataTransparent process Cell softness regulates tumorigenicity and stemness of cancer cells Jiadi Lv Department Immunology & National Key Laboratory Medical Molecular Biology, Institute Basic Sciences, Chinese Academy Sciences (CAMS) Peking Union College, Beijing, ChinaThese authors contributed equally to this work Search for more papers by author Yaoping Liu Microelectronics, University, Feiran Cheng orcid.org/0000-0001-9460-9949 Jiping Li Beijing...

10.15252/embj.2020106123 article EN cc-by The EMBO Journal 2020-12-04

Dynamic interaction with the immune system profoundly regulates tumor cell dormancy. However, it is unclear how immunological cues trigger cancer cell–intrinsic signaling pathways for entering into Here, we show that IFN-β treatment induced tumor-repopulating cells (TRC) to enter dormancy through an indolamine 2,3-dioxygenase/kynurenine/aryl hydrocarbon receptor/p27–dependent (IDO/Kyn/AhR/p27-dependent) pathway. Strategies block this metabolic circuitry did not relieve dormancy, but led...

10.1172/jci96329 article EN Journal of Clinical Investigation 2018-02-11

Abstract Dormancy is recognized as a critical biological event for tumorigenic cells surviving in an extremely harsh environment. Understanding the molecular process of dormancy can unlock novel approaches to tackle cancers. We recently reported that stem-like tumor-repopulating (TRC) sense mechanical signals and rapidly proliferate 90 Pa soft fibrin matrix. Here, we show stiff environment induces TRC via epigenetic program initiated by translocation Cdc42, cytosolic regulator...

10.1158/0008-5472.can-17-3719 article EN Cancer Research 2018-05-15

Abstract Biomechanics is a fundamental feature of cell. However, the manner by which actomysin tension affects tumor immune evasion remains unclear. Here we show that although cytotoxic T lymphocytes (CTL) can effectively destroy stiff differentiated cells, they fail to kill soft tumor-repopulating cells (TRC). TRC softness prevented membrane pore formation caused CTL-released perforin. Perforin interacting with nonmuscle myosin heavy-chain 9 transmitted forces less F-actins in TRC, thus...

10.1158/0008-5472.can-20-2569 article EN Cancer Research 2020-11-09

Abstract Hypoxia is known to be commonly present in breast tumor microenvironments. Stem-like cells that repopulate tumors, termed tumor-repopulating (TRC), thrive under hypoxic conditions, but the underlying mechanism remains unclear. Here, we show hypoxia promotes growth of TRCs through metabolic reprogramming. mobilized transcription factors HIF1α and FoxO1 induced epigenetic reprogramming upregulate cytosolic phosphoenolpyruvate carboxykinase (PCK1), a key enzyme initiates...

10.1158/0008-5472.can-21-0753 article EN Cancer Research 2021-08-04

Clear cell renal carcinoma (ccRCC) is a common malignant tumour of the urinary tract. The major causes poor prognosis are lack early diagnosis and metastasis. Accumulating research reveals that circular RNAs (circRNAs) can play key roles in development progression cancer. However, role circRNAs ccRCC still uncertain.The microarray (n = 4) was performed to investigate with differential expression tissues. candidate circRNA selected based on cut-off criteria, such as abundance, size design...

10.1002/ctm2.994 article EN cc-by Clinical and Translational Medicine 2022-07-01

Abstract Background Gastric cancer (GC) is one of the most common malignant tumors in China. Circular RNAs (circRNAs) are novel non-coding with important regulatory roles progression. IGF2BP3 has been found to play oncogenic various cancers including GC, while exact mechanism largely unknown. Methods The expression GC was evaluated by Western Blot and bioinformatics analysis. CircRNA profiles were screened via RIP-seq GC. Sanger sequencing, RNase R digestion, nucleo-plasmic separation...

10.1186/s13046-022-02466-3 article EN cc-by Journal of Experimental & Clinical Cancer Research 2022-08-19

Abstract Background Insulin like growth factor II mRNA binding protein 3 (IGF2BP3) is an RNA with multiple roles in regulation of gene expression at the post-transcriptional level and implicated tumorigenesis progression numerous cancers including gastric cancer (GC). Circular RNAs (circRNAs) are a diverse endogenous noncoding population that have important regulatory cancer. However, circRNAs regulate IGF2BP3 GC largely unknown. Methods CircRNAs bound to were screened cells using...

10.1186/s12967-023-04235-y article EN cc-by Journal of Translational Medicine 2023-06-20

Abstract Background Clear cell renal carcinoma (ccRCC) is the most prevalent kidney cancer with high aggressive phenotype and poor prognosis. Accumulating evidence suggests that circRNAs have been identified as pivotal mediators in cancers. However, role of ccRCC progression remains elusive. Methods The differentially expressed 4 paired human adjacent noncancerous tissues were screened using circRNA microarrays candidate target was selected based on expression level weighted gene correlation...

10.1186/s12943-024-01940-0 article EN cc-by Molecular Cancer 2024-02-15
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