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  1. Home
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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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서비스
WGSDe novo SeqAmplicon SeqShotgun MetagenomeDM-SeqmRNA-SeqSingle Cell Gene ExpressionVisium HDXenium In SituOlinkUntargeted Metabolomics
고객지원
노보매직CSSFalcon 플랫폼
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Copyright © 2026 Novogene Co., Ltd. All Rights Reserved. 노보진의 한국 내 모든 서비스는 연구 목적 (Research Use Only, RUO) 으로만 제공됩니다. 사업자등록번호: 494-86-03792 | 판매자번호: 노보진코리아유한회사 | 대표자명: 리휘시앙 | 사업자주소: 서울시 강서구 마곡동 779-1번지 뉴브클라우드힐스 BT-230, 231호, 07790 | 전화번호: 02-2038-8036
Novogene Korea
  • Novogene Korea
  • Genomics
    • Human Whole Genome Sequencing
    • Plant & Animal Whole Genome Sequencing
    • Microbial Whole Genome Sequencing
    • Whole Exome Sequencing
    • Plant & Animal De novo Sequencing
    • Microbial De novo Sequencing
    • Amplicon Sequencing
    • Shotgun Metagenomics 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 (Illumina 플랫폼)
    • Sequencing Only (PacBio 플랫폼)
    Proteomics & Metabolomics
    • Olink Proteomics
    • Quantitative Proteomics (MS)
    • Untargeted Metabolomics (MS)
  • 프로모션프로모션
    • 플랫폼
    • 자동화 운송 플랫폼 (Falcon)
    • BI 분석툴 (NovoMagic)
    • Customer Service System (CSS)
    • 브로셔
    • 케이스 스터디
    • 웨비나
    • 블로그
    • 샘플준비 가이드라인
    • 커뮤니티
    • 암 연구
    • 면역 종양학
    • 농업
    • 환경
    • 식품
    • 인간 마이크로바이옴
    • 동물 & 식물 마이크로바이옴
    • 신약개발
    • 희귀 질환 연구
    • 회사소개
    • 글로벌 입지
    • 뉴스룸
    • 채용 정보
  • 문의하기문의하기
  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

서비스서비스 menu

고객지원고객지원 menu

기업정보기업정보 menu

서비스
WGSDe novo SeqAmplicon SeqShotgun MetagenomeDM-SeqmRNA-SeqSingle Cell Gene ExpressionVisium HDXenium In SituOlinkUntargeted Metabolomics
고객지원
노보매직CSSFalcon 플랫폼
기업정보
회사소개글로벌 입지플랫폼뉴스룸채용 정보문의하기
LinkedInLinkedIn hoverYouTubeYouTube hoverXX hoverMetaMeta hoverInstagramInstagram hover
Copyright © 2026 Novogene Co., Ltd. All Rights Reserved. 노보진의 한국 내 모든 서비스는 연구 목적 (Research Use Only, RUO) 으로만 제공됩니다. 사업자등록번호: 494-86-03792 | 판매자번호: 노보진코리아유한회사 | 대표자명: 리휘시앙 | 사업자주소: 서울시 강서구 마곡동 779-1번지 뉴브클라우드힐스 BT-230, 231호, 07790 | 전화번호: 02-2038-8036
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