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  3. Addressing the new role of cytidine deaminase in pancreatic cancer using transcriptomics

Addressing the new role of cytidine deaminase in pancreatic cancer using transcriptomics

Speaker Introduction:

Dr Pierre Cordelier, PhD in Human Physiopathology, is Research Director at INSERM, team leader (ther-apeutic innovation in pancreatic cancer) and deputy director of the cancer research centre of Toulouse(CRCT). Dr Cordelier research focus is to identify the molecular mechanisms involved into pancreatictumors oncogenesis and resistance to treatment, to advocate for personalized therapies and help alle-viate the dismal prognosis of this disease with no cure.

Topic Introduction:

The objective of this research program is to identify the role of cytidine deaminase, an enzyme otherwise involved in tumor resistance to gemcitabine, is exerting in pancreatic cancer cells

Description:

Chronic DNA replication stress and genome instability are two hallmarks of cancer that fuel oncogene sis and tumor diversity. Therapeutic approaches aimed to leverage tumor-specific replication stress to intolerable levels or to expose vulnerabilities for synthetic lethality purpose have recently gained mo mentum, especially for pancreatic cancer, a disease with no cure. However, the current knowledge is limited considering the molecular mechanisms involved in the replication stress response in pancreat ic tumors. Cytidine deaminase (CDA) is involved in the pyrimidine salvage pathway for DNA and RNA synthesis. Loss of CDA induces genomic instability in Bloom Syndrome, and CDA protects tumor cells from chemotherapy with pyrimidine analogs. Here, we show that CDA is overexpressed in genetically instable pancreatic tumors, associates with DNA replication signature and is instrumental for experi mental tumor growth. In cancer cells, CDA promotes DNA replication, increases replication fork fitness for controlling replication stress and genomic stability. CDA expression is predictive of DNA-damaging drug efficacy, and targeting CDA relieves resistance to chemotherapy in patients’ models. Our findings shed a new light on the mechanisms by which pancreatic cancer cells control replication stress, and highlight targeting of CDA as a potential therapeutic intervention to defeat tumor resistance to treat ment.

From this webinar, you will:

  • Understand the role of cytidine deaminase in healthy and cancerous cells.
  • Learn about the mechanisms by which pancreatic cancer cells control replication stress
  • Discover potential therapeutic interventions to defeat tumor resistance to treatment

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Whole Genome SequencingDe novo SequencingAmplicon SequencingShotgun Metagenomic SequencingDirected DNA Methylation Sequencing (DM-Seq)mRNA SequencingSingle Cell Gene ExpressionVisium HD Spatial Gene ExpressionXenium In Situ Spatial TranscriptomeOlink ProteomicsUntargeted Metabolomics
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Copyright © 2026 Novogene Inc. All rights reserved.For Research Use Only. Not for Clinical Diagnostic Use.
Novogene AMEA
  • Novogene AMEA
  • Genomics
    • Human Whole Genome Sequencing
    • Plant and Animal Whole Genome Sequencing
    • Microbial Whole Genome Sequencing
    • Plant and Animal De novo Sequencing
    • Microbial De novo Sequencing
    • Shotgun Metagenomics Sequencing
    • Amplicon Sequencing
    • Whole Exome Sequencing
    Transcriptomics
    • mRNA Sequencing
    • Total RNA Sequencing
    • Full-Length Transcriptome Sequencing
    • Whole Transcriptome Sequencing
    • Small RNA Sequencing
    • Circular RNA Sequencing
    • Metatranscriptome Sequencing
    • Prokaryotic RNA Sequencing
    Single Cell & Spatial Omics
    • Single Cell Gene Expression
    • Single Cell Immune Profiling Sequencing
    • Single Cell Long Read Transcriptome
    • Visium HD Spatial Gene Expression
    • Stereo-Seq Spatial Gene Expression
    • Xenium In Situ Spatial Transcriptome
    Epigenomics
    • Whole Genome Bisulfite Sequencing (WGBS)
    • Directed DNA Methylation Sequencing (DM-Seq) NEW
    • Reduced Representation Bisulfite Sequencing (RRBS)
    • Chromatin Immunoprecipitation Sequencing (ChIP-seq)
    • RNA Immunoprecipitation Sequencing (RIP-seq)
    • Assay for Transposase-Accessible Chromatin with Sequencing (ATAC-seq)

    Premade Library

    • Sequencing Only on Illumina Sequencer
    • Sequencing Only on PacBio Sequencer
    Proteomics and Metabolomics
    • Olink Proteomics
    • Quantitative Proteomics
    • Untargeted Metabolomics
  • PromotionsPromotions
    • Platforms
    • Automated Delivery Platform (Falcon)
    • Bioinformatics Analysis Tool (NovoMagic)
    • Customer Service System (CSS)
    • Brochures
    • Case Studies
    • Webinar
    • Blog
    • Sample Guidelines
    • Cancer Research
    • Immuno-oncology
    • Agrigenomics
    • Environment
    • Food Science
    • Human Microbiome
    • Plant and Animal Microbiome
    • Drug Discovery and Development
    • Rare and Complex Diseases
    • About Us
    • Our Locations
    • News
    • Careers
  • Contact UsContact Us
  1. Home
  2. Resources
  3. Addressing the new role of cytidine deaminase in pancreatic cancer using transcriptomics

Addressing the new role of cytidine deaminase in pancreatic cancer using transcriptomics

Speaker Introduction:

Dr Pierre Cordelier, PhD in Human Physiopathology, is Research Director at INSERM, team leader (ther-apeutic innovation in pancreatic cancer) and deputy director of the cancer research centre of Toulouse(CRCT). Dr Cordelier research focus is to identify the molecular mechanisms involved into pancreatictumors oncogenesis and resistance to treatment, to advocate for personalized therapies and help alle-viate the dismal prognosis of this disease with no cure.

Topic Introduction:

The objective of this research program is to identify the role of cytidine deaminase, an enzyme otherwise involved in tumor resistance to gemcitabine, is exerting in pancreatic cancer cells

Description:

Chronic DNA replication stress and genome instability are two hallmarks of cancer that fuel oncogene sis and tumor diversity. Therapeutic approaches aimed to leverage tumor-specific replication stress to intolerable levels or to expose vulnerabilities for synthetic lethality purpose have recently gained mo mentum, especially for pancreatic cancer, a disease with no cure. However, the current knowledge is limited considering the molecular mechanisms involved in the replication stress response in pancreat ic tumors. Cytidine deaminase (CDA) is involved in the pyrimidine salvage pathway for DNA and RNA synthesis. Loss of CDA induces genomic instability in Bloom Syndrome, and CDA protects tumor cells from chemotherapy with pyrimidine analogs. Here, we show that CDA is overexpressed in genetically instable pancreatic tumors, associates with DNA replication signature and is instrumental for experi mental tumor growth. In cancer cells, CDA promotes DNA replication, increases replication fork fitness for controlling replication stress and genomic stability. CDA expression is predictive of DNA-damaging drug efficacy, and targeting CDA relieves resistance to chemotherapy in patients’ models. Our findings shed a new light on the mechanisms by which pancreatic cancer cells control replication stress, and highlight targeting of CDA as a potential therapeutic intervention to defeat tumor resistance to treat ment.

From this webinar, you will:

  • Understand the role of cytidine deaminase in healthy and cancerous cells.
  • Learn about the mechanisms by which pancreatic cancer cells control replication stress
  • Discover potential therapeutic interventions to defeat tumor resistance to treatment

ServicesServices menu

SupportSupport menu

CompanyCompany menu

Services
Whole Genome SequencingDe novo SequencingAmplicon SequencingShotgun Metagenomic SequencingDirected DNA Methylation Sequencing (DM-Seq)mRNA SequencingSingle Cell Gene ExpressionVisium HD Spatial Gene ExpressionXenium In Situ Spatial TranscriptomeOlink ProteomicsUntargeted Metabolomics
Support
NovoMagic Bioinformatics Analysis ToolCustomer Service SystemFalcon Intelligent Delivery Platform
Company
About UsOur LocationsOur PlatformsNewsCareersContact Us
LinkedInLinkedIn hoverYouTubeYouTube hoverXX hover
Copyright © 2026 Novogene Inc. All rights reserved.For Research Use Only. Not for Clinical Diagnostic Use.
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