Hui Yuan

ORCID: 0000-0001-5462-7042
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About
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Research Areas
  • Macrophage Migration Inhibitory Factor
  • Nuclear Receptors and Signaling
  • GDF15 and Related Biomarkers
  • Biochemical Acid Research Studies
  • Cancer-related molecular mechanisms research
  • Apelin-related biomedical research
  • Machine Learning and Algorithms
  • Circular RNAs in diseases
  • RNA Research and Splicing
  • Cancer-related Molecular Pathways
  • Statistical Methods and Inference
  • Advanced Breast Cancer Therapies
  • Sparse and Compressive Sensing Techniques
  • RNA modifications and cancer
  • Atomic and Molecular Physics
  • MicroRNA in disease regulation
  • Advanced Chemical Physics Studies
  • Distributed Sensor Networks and Detection Algorithms
  • HER2/EGFR in Cancer Research
  • Medicinal Plant Pharmacodynamics Research
  • Machine Learning and Data Classification
  • Radiomics and Machine Learning in Medical Imaging
  • Molecular Spectroscopy and Structure
  • Inorganic Fluorides and Related Compounds
  • Advanced Statistical Methods and Models

Anhui Medical University
2025

Second Hospital of Anhui Medical University
2025

Chongqing Medical University
2025

University of Science and Technology of China
2003-2024

Sunnybrook Health Science Centre
2024

Health Sciences Centre
2024

University of Toronto
2024

Sunnybrook Research Institute
2024

Anhui University
2009

Abstract Reprogramming of energy metabolism exerts pivotal functions in cancer progression and immune surveillance. Identification the mechanisms mediating metabolic changes may lead to improved strategies suppress tumor growth stimulate antitumor immunity. Here, it was observed that secretomes hypoxic breast cells stem (BCSC) induced reprogramming pathways, particularly glycolysis, normoxic cells. Screening BCSC secretome identified MIF as a factor potentiating glycolysis. Mechanistically,...

10.1158/0008-5472.can-23-2390 article EN Cancer Research 2024-02-09

Although tamoxifen is commonly utilized as adjuvant therapy for Estrogen Receptor alpha (ERα)-positive breast cancer patients, approximately 30–50% of individuals treated with experience relapse. Therefore, it essential to investigate additional factors besides ERα that influence the estrogen response. In this study, cross-analysis databases were performed, and results revealed a significant association between LINC00626 signaling well increased expression levels gene in tamoxifen-resistant...

10.1038/s41598-025-86287-2 article EN cc-by-nc-nd Scientific Reports 2025-01-23

Abstract Resistance to chemotherapy remains a major obstacle the successful treatment of breast cancer. More than 80% patients who receive neoadjuvant (NAC) do not achieve pathologic complete response. In this study, we report novel p62 mRNA isoform with short 3′-UTR (untranslated region; p62-SU, 662-nt) that is associated chemoresistance in cancer cells and tissue specimens. The was identified by RNA sequencing qRT-PCR, 3′-RACE, Northern blot analysis. vitro vivo, ectopic expression p62-SU...

10.1158/0008-5472.can-22-0909 article EN Cancer Research 2022-08-29

<div>Abstract<p>Reprogramming of energy metabolism exerts pivotal functions in cancer progression and immune surveillance. Identification the mechanisms mediating metabolic changes may lead to improved strategies suppress tumor growth stimulate antitumor immunity. Here, it was observed that secretomes hypoxic breast cells stem (BCSC) induced reprogramming pathways, particularly glycolysis, normoxic cells. Screening BCSC secretome identified MIF as a factor potentiating...

10.1158/0008-5472.c.7181269.v2 preprint EN 2024-04-15

Abstract Estrogen receptor alpha (ERα) plays a vital role in the development of normal breast tissue and cancer. By cross-analyzing The Cancer Genome Atlas (TCGA) database, ERα-regulated long noncoding RNA 1 (ERLC1) was identified as exhibiting strong association with ERα signaling high specificity expression tissue. ERLC1 transcriptionally activated by ERα, stabilized ESR1 transcript sequestering miR-129 tethering FXR1 to maintain positive feedback loop that potentiated signaling. elevated...

10.1158/0008-5472.can-21-1155 article EN Cancer Research 2021-11-22

The valence shell excitations of argon were investigated by an angle-resolved fast-electron energy-loss spectrometer at incident electron energy $2500\phantom{\rule{0.3em}{0ex}}\mathrm{eV}$, and the transition multipolarities for $3p\ensuremath{\rightarrow}3d$, $4d$, $5s$, $5p$ elucidated with help calculated intermediate coupling coefficients using COWAN code. generalized oscillator strengths to $3{p}^{5}(3d,3{d}^{\ensuremath{'}})$, $3{p}^{5}(5p,5{p}^{\ensuremath{'}})$, $3{p}^{5}(5s,4d)$...

10.1103/physreva.75.032701 article EN Physical Review A 2007-03-05

<p>Supplementary Figure S4 shows that MIF secreted by BCSCs to enhance the glycolysis of breast cancer cells.</p>

10.1158/0008-5472.25607427 preprint EN cc-by 2024-04-15

<p>Supplementary Figure S2 shows that BCSC CM enhances the aerobic glycolysis not oxidative phosphorylation.</p>

10.1158/0008-5472.25607433 preprint EN cc-by 2024-04-15

<p>Table S1 shows the sequences of sgRNAs, shRNAs and primers for cloning qRT-PCR analysis.</p>

10.1158/0008-5472.25607412.v1 preprint EN cc-by 2024-04-15

<p>Supplementary Figure S6 shows that BCSCs regulate cancer cell metabolic reprogramming through ALDOC.</p>

10.1158/0008-5472.25607421.v1 preprint EN cc-by 2024-04-15

<p>Supplementary Figure S8 shows that Targeting MIF enhances cancer cell sensitivity to immune killing.</p>

10.1158/0008-5472.25607415.v1 preprint EN cc-by 2024-04-15

<div>Abstract<p>Reprogramming of energy metabolism exerts pivotal functions in cancer progression and immune surveillance. Identification the mechanisms mediating metabolic changes may lead to improved strategies suppress tumor growth stimulate antitumor immunity. Here, it was observed that secretomes hypoxic breast cells stem (BCSC) induced reprogramming pathways, particularly glycolysis, normoxic cells. Screening BCSC secretome identified MIF as a factor potentiating...

10.1158/0008-5472.c.7181269.v1 preprint EN 2024-04-15

<p>Supplementary Figure S4 shows that MIF secreted by BCSCs to enhance the glycolysis of breast cancer cells.</p>

10.1158/0008-5472.25607427.v1 preprint EN cc-by 2024-04-15
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