L. H. GINN

ORCID: 0000-0002-8673-339X
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About
Contact & Profiles
Research Areas
  • Historical and Literary Studies
  • RNA modifications and cancer
  • Cancer-related molecular mechanisms research
  • RNA Research and Splicing
  • Cytokine Signaling Pathways and Interactions
  • PI3K/AKT/mTOR signaling in cancer
  • Cellular Mechanics and Interactions
  • HER2/EGFR in Cancer Research
  • Ubiquitin and proteasome pathways
  • Cancer-related gene regulation
  • Lung Cancer Treatments and Mutations
  • interferon and immune responses
  • RNA regulation and disease
  • Cancer Cells and Metastasis
  • Protein Kinase Regulation and GTPase Signaling

University of Manchester
2020-2024

Cancer Research UK
2020-2024

Cancer Research UK Manchester Institute
2020-2024

University of Sheffield
1984-2022

CRUK Lung Cancer Centre of Excellence
2020

University College London
2020

Lung cancer is the leading cause of deaths. Its high mortality associated with metastatic potential. Here, we show that RAC1-selective guanine nucleotide exchange factor T cell invasion and metastasis-inducing protein 1 (TIAM1) promotes migration in most common subtype lung cancer, non-small-cell (NSCLC), through an unexpected nuclear function. We TIAM1 interacts TRIM28, a master regulator gene expression, nucleus NSCLC cells. reveal TIAM1-TRIM28 complex epithelial-to-mesenchymal transition,...

10.1073/pnas.2300489120 article EN cc-by Proceedings of the National Academy of Sciences 2023-09-25

Summary Viral infection leads to large alterations in the host transcriptome and stimulates an antiviral immune response involving numerous proteins signalling pathways. Long non‐coding RNAs (lncRNAs) have emerged as important regulators during viral infection. Emerging data demonstrates that lncRNAs play essential roles at pathogen interface modulating by either distinct level including recognition receptors or epigenetic, transcriptional, post‐transcriptional effects. Furthermore,...

10.1002/rmv.2198 article EN Reviews in Medical Virology 2020-11-27

KRASG12C and KRASG12D inhibitors represent a major translational breakthrough for non-small cell lung cancer (NSCLC) in general by directly targeting its most mutated oncoprotein. However, resistance to these small molecules has highlighted the need rational combination partners necessitating critical understanding of signaling downstream KRAS mutant isoforms. We contrasted tumor development between KrasG12C KrasG12D genetically engineered mouse models (GEMMs). To corroborate findings...

10.1186/s12943-024-02157-x article EN cc-by Molecular Cancer 2024-11-12

Chemoresistance poses a great barrier to breast cancer treatment and is thought correlate with increased matrix stiffness. We developed two-dimensional (2D) polyacrylamide (PAA) three-dimensional (3D) alginate in vitro models of tissue stiffness that mimic the normal cancer. then used these compare cell viability response chemotherapeutic treatment. In both 2D 3D we observed growth size was at higher corresponding tumours compared tissue. When measured, specific differential for gemcitabine...

10.1371/journal.pone.0268300 article EN cc-by PLoS ONE 2022-05-26

Abstract Introduction KRAS G12C and G12D inhibitors represent a major translational breakthrough for non-small cell lung cancer (NSCLC) in general by directly targeting its most mutated oncoprotein. However, resistance to these small molecules has highlighted the need rational combination partners necessitating critical understanding of signaling downstream mutant isoforms. Methods We contrasted tumor development between Kras genetically engineered mouse models (GEMMs). To corroborate...

10.1101/2023.09.20.558592 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-09-22

10.1163/22224297-90002634 article EN The Year’s Work in Modern Language Studies 1985-03-13

10.1163/22224297-90002559 article EN The Year’s Work in Modern Language Studies 1984-03-13

10.1163/22224297-90002713 article EN The Year’s Work in Modern Language Studies 1986-03-13

10.1163/22224297-90002789 article EN The Year’s Work in Modern Language Studies 1987-03-13

10.1163/22224297-90002868 article EN The Year’s Work in Modern Language Studies 1988-03-13
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