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Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord.
Wang, Yuxuan; Springer, Simeon; Zhang, Ming; McMahon, K Wyatt; Kinde, Isaac; Dobbyn, Lisa; Ptak, Janine; Brem, Henry; Chaichana, Kaisorn; Gallia, Gary L; Gokaslan, Ziya L; Groves, Mari L; Jallo, George I; Lim, Michael; Olivi, Alessandro; Quinones-Hinojosa, Alfredo; Rigamonti, Daniele; Riggins, Greg J; Sciubba, Daniel M; Weingart, Jon D; Wolinsky, Jean-Paul; Ye, Xiaobu; Oba-Shinjo, Sueli Mieko; Marie, Suely K N; Holdhoff, Matthias; Agrawal, Nishant; Diaz, Luis A; Papadopoulos, Nickolas; Kinzler, Kenneth W; Vogelstein, Bert; Bettegowda, Chetan.
Afiliação
  • Wang Y; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Springer S; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Zhang M; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • McMahon KW; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Kinde I; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Dobbyn L; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Ptak J; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Brem H; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Chaichana K; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Gallia GL; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Gokaslan ZL; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Groves ML; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Jallo GI; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Lim M; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Olivi A; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Quinones-Hinojosa A; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Rigamonti D; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Riggins GJ; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Sciubba DM; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Weingart JD; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Wolinsky JP; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Ye X; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Oba-Shinjo SM; Department of Neurology and Pathology, School of Medicine, University of Sao Paulo, Sao Paulo, SP 01246-903, Brazil;
  • Marie SK; Department of Neurology and Pathology, School of Medicine, University of Sao Paulo, Sao Paulo, SP 01246-903, Brazil;
  • Holdhoff M; Department of Oncology, Brain Cancer Division, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Agrawal N; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287.
  • Diaz LA; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Papadopoulos N; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Kinzler KW; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287;
  • Vogelstein B; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287; bertvog@gmail.com cbetteg1@jhmi.edu.
  • Bettegowda C; Ludwig Center, Howard Hughes Medical Institute and the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287; Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287; bertvog@gmail.com cbetteg1@jhmi.edu.
Proc Natl Acad Sci U S A ; 112(31): 9704-9, 2015 Aug 04.
Article em En | MEDLINE | ID: mdl-26195750
Cell-free DNA shed by cancer cells has been shown to be a rich source of putative tumor-specific biomarkers. Because cell-free DNA from brain and spinal cord tumors cannot usually be detected in the blood, we studied whether the cerebrospinal fluid (CSF) that bathes the CNS is enriched for tumor DNA, here termed CSF-tDNA. We analyzed 35 primary CNS malignancies and found at least one mutation in each tumor using targeted or genome-wide sequencing. Using these patient-specific mutations as biomarkers, we identified detectable levels of CSF-tDNA in 74% [95% confidence interval (95% CI) = 57-88%] of cases. All medulloblastomas, ependymomas, and high-grade gliomas that abutted a CSF space were detectable (100% of 21 cases; 95% CI = 88-100%), whereas no CSF-tDNA was detected in patients whose tumors were not directly adjacent to a CSF reservoir (P < 0.0001, Fisher's exact test). These results suggest that CSF-tDNA could be useful for the management of patients with primary tumors of the brain or spinal cord.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Medula Espinal / Neoplasias Encefálicas / DNA de Neoplasias Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Medula Espinal / Neoplasias Encefálicas / DNA de Neoplasias Idioma: En Ano de publicação: 2015 Tipo de documento: Article