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Quantifiable TCR repertoire changes in prediagnostic blood specimens among patients with high-grade ovarian cancer.
Yu, Xuexin; Pan, Mingyao; Ye, Jianfeng; Hathaway, Cassandra A; Tworoger, Shelley S; Lea, Jayanthi; Li, Bo.
Afiliación
  • Yu X; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Pathology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Pan M; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Pathology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Ye J; Department of Neuroscience, UT Southwestern Medical Center, Dallas, TX 75390, USA.
  • Hathaway CA; Department of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL 33612, USA.
  • Tworoger SS; Knight Cancer Institute and Division of Oncological Sciences, Oregon Health & Science University, Portland, OR 97239, USA.
  • Lea J; Department of Gynecology, UT Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address: jayanthi.lea@utsouthwestern.edu.
  • Li B; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Pathology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: libo2@pennmedicine.upenn.edu.
Cell Rep Med ; 5(7): 101612, 2024 Jul 16.
Article en En | MEDLINE | ID: mdl-38878776
ABSTRACT
High-grade ovarian cancer (HGOC) is a major cause of death in women. Early detection of HGOC usually leads to a cure, yet it remains a clinical challenge with over 90% HGOCs diagnosed at advanced stages. This is mainly because conventional biomarkers are not sensitive enough to detect the microscopic yet metastatic early lesions. In this study, we sequence the bloodcell receptor (TCR) repertoires of 466 patients with ovarian cancer and controls and systematically investigate the immune repertoire signatures in HGOCs. We observe quantifiable changes of selected TCRs in HGOCs that are reproducible in multiple independent cohorts. Importantly, these changes are stronger during stage I. Using pre-diagnostic patient blood samples from the Nurses' Health Study, we confirm that HGOC signals can be detected in the blood TCR repertoire up to 4 years preceding conventional diagnosis. Our findings may provide the basis for future immune-based HGOC early detection criteria.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Receptores de Antígenos de Linfocitos T Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Cell Rep Med Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Receptores de Antígenos de Linfocitos T Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Cell Rep Med Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos