Shu-Fang Guo

ORCID: 0009-0009-2682-0318
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About
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Research Areas
  • Cancer-related molecular mechanisms research
  • Immune Cell Function and Interaction
  • Radiomics and Machine Learning in Medical Imaging
  • Lung Cancer Diagnosis and Treatment
  • Multiple Myeloma Research and Treatments
  • Statistical Methods in Clinical Trials
  • Heavy Metal Exposure and Toxicity
  • Extracellular vesicles in disease
  • Heavy metals in environment
  • CAR-T cell therapy research
  • Atomic and Subatomic Physics Research
  • COVID-19 diagnosis using AI
  • Air Quality and Health Impacts
  • Medication Adherence and Compliance
  • Integrated Circuits and Semiconductor Failure Analysis
  • Diabetes Treatment and Management

Wuhan Polytechnic University
2024-2025

Zhengzhou Children's Hospital
2024

Zhengzhou University
2024

Nanchang University
2023

University of Pittsburgh
2023

Abstract Background Extensive research has explored the association between heavy metal exposure and various health outcomes, including malignant neoplasms, hypertension, diabetes, heart diseases. This study aimed to investigate relationship patterns of a mixture seven metals these outcomes. Methods Blood samples from 7,236 adults in NHANES 2011–2016 studies were analyzed for levels cadmium, manganese, lead, mercury, selenium, copper, zinc. Cluster analysis logistic regression identified...

10.1186/s12889-024-17754-0 article EN cc-by BMC Public Health 2024-02-22

Abstract Exosomal long noncoding RNAs (lncRNA) derived from cancer cells are implicated in various processes, including cell proliferation, metastasis, and immunomodulation. We investigated the role underlying mechanism of exosome-transmitted lncRNA NEAT1 immune escape multiple myeloma natural killer (NK) cells. Multiple samples patients with were obtained. The effects cell-derived exosomes (multiple exosomes) exosomal on functions NK evaluated using EdU staining, CCK-8, flow cytometry,...

10.1158/1541-7786.mcr-23-0282 article EN Molecular Cancer Research 2023-10-26

Abstract Chimeric antigen receptor T (CAR-T) cells therapy has made remarkable progress in relapsed/refractory multiple myeloma (R/R MM) treatment. Unfortunately, patients still eventually experience disease progression or relapse even after receiving anti-BCMA CAR-T therapy. At present, there are limited data on available treatment options for who have progressed In this study, we evaluated the safety and efficacy of fully human (HRC0202) seven R/R MM were previously exposed to Three...

10.1038/s41417-023-00712-0 article EN cc-by Cancer Gene Therapy 2023-12-15

<div>Abstract<p>Exosomal long noncoding RNAs (lncRNA) derived from cancer cells are implicated in various processes, including cell proliferation, metastasis, and immunomodulation. We investigated the role underlying mechanism of exosome-transmitted lncRNA NEAT1 immune escape multiple myeloma natural killer (NK) cells. Multiple samples patients with were obtained. The effects cell-derived exosomes (multiple exosomes) exosomal on functions NK evaluated using EdU staining, CCK-8,...

10.1158/1541-7786.c.7054183 preprint EN 2024-02-01

10.1109/bibm62325.2024.10822571 article EN 2021 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) 2024-12-03

<p>Supplementary Figure 4 shows that NK cells treated with MM exosomes released from U266 could modulate cell function through regulating PBX1.</p>

10.1158/1541-7786.25124947 preprint EN cc-by 2024-02-01

<p>Supplementary Figure 4 shows that NK cells treated with MM exosomes released from U266 could modulate cell function through regulating PBX1.</p>

10.1158/1541-7786.25124947.v1 preprint EN cc-by 2024-02-01

<p>Supplementary Figure 2 shows that MM exosomes derived from U266 cells or NEAT1 knockdown had no effect on EZH2 expression.</p>

10.1158/1541-7786.25124953 preprint EN cc-by 2024-02-01

<p>Supplementary Figure 2 shows that MM exosomes derived from U266 cells or NEAT1 knockdown had no effect on EZH2 expression.</p>

10.1158/1541-7786.25124953.v1 preprint EN cc-by 2024-02-01

<p>Supplementary Figure 1 shows that MM exosomes derived from U266 cells inhibit the proliferation and activity of NK but enhance cells’ apoptosis, while NEAT1 knockdown have lost this function.</p>

10.1158/1541-7786.25124959.v1 preprint EN cc-by 2024-02-01

<p>Supplementary Figure 3 shows that MM exosomes derived from U266 cells NEAT1 knockdown ehance the proliferation and activity of NK but suppress cells’ apoptosis, while PBX1 reverses this function.</p>

10.1158/1541-7786.25124950 preprint EN cc-by 2024-02-01

<p>Supplementary Figure 1 shows that MM exosomes derived from U266 cells inhibit the proliferation and activity of NK but enhance cells’ apoptosis, while NEAT1 knockdown have lost this function.</p>

10.1158/1541-7786.25124959 preprint EN cc-by 2024-02-01

<p>Supplementary Figure 3 shows that MM exosomes derived from U266 cells NEAT1 knockdown ehance the proliferation and activity of NK but suppress cells’ apoptosis, while PBX1 reverses this function.</p>

10.1158/1541-7786.25124950.v1 preprint EN cc-by 2024-02-01

<div>Abstract<p>Exosomal long noncoding RNAs (lncRNA) derived from cancer cells are implicated in various processes, including cell proliferation, metastasis, and immunomodulation. We investigated the role underlying mechanism of exosome-transmitted lncRNA NEAT1 immune escape multiple myeloma natural killer (NK) cells. Multiple samples patients with were obtained. The effects cell-derived exosomes (multiple exosomes) exosomal on functions NK evaluated using EdU staining, CCK-8,...

10.1158/1541-7786.c.7054183.v1 preprint EN 2024-02-01

10.1109/bibm62325.2024.10822144 article EN 2021 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) 2024-12-03
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