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  1. TI=RNA Seq of Tumor Educated Platelets Enables Blood Based Pan Cancer Multiclass and Molecular Pathway Cancer Diagnostics
  2. AU="Larissa J Osterbann"

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Artikel ; Online: RNA-Seq of Tumor-Educated Platelets Enables Blood-Based Pan-Cancer, Multiclass, and Molecular Pathway Cancer Diagnostics.

Best, Myron G / Sol, Nik / Kooi, Irsan / Tannous, Jihane / Westerman, Bart A / Rustenburg, François / Schellen, Pepijn / Verschueren, Heleen / Post, Edward / Koster, Jan / Ylstra, Bauke / Ameziane, Najim / Dorsman, Josephine / Smit, Egbert F / Verheul, Henk M / Noske, David P / Reijneveld, Jaap C / Nilsson, R Jonas A / Tannous, Bakhos A /
Wesseling, Pieter / Wurdinger, Thomas

Cancer cell

2015  Band 28, Heft 5, Seite(n) 666–676

Abstract: Tumor-educated blood platelets (TEPs) are implicated as central players in the systemic and local ... Our results indicate that blood platelets provide a valuable platform for pan-cancer, multiclass cancer, and ... companion diagnostics, possibly enabling clinical advances in blood-based "liquid biopsies". ...

Abstract Tumor-educated blood platelets (TEPs) are implicated as central players in the systemic and local responses to tumor growth, thereby altering their RNA profile. We determined the diagnostic potential of TEPs by mRNA sequencing of 283 platelet samples. We distinguished 228 patients with localized and metastasized tumors from 55 healthy individuals with 96% accuracy. Across six different tumor types, the location of the primary tumor was correctly identified with 71% accuracy. Also, MET or HER2-positive, and mutant KRAS, EGFR, or PIK3CA tumors were accurately distinguished using surrogate TEP mRNA profiles. Our results indicate that blood platelets provide a valuable platform for pan-cancer, multiclass cancer, and companion diagnostics, possibly enabling clinical advances in blood-based "liquid biopsies".
Mesh-Begriff(e) Adult ; Aged ; Aged, 80 and over ; Biomarkers, Tumor/blood ; Biomarkers, Tumor/genetics ; Blood Platelets/metabolism ; Class I Phosphatidylinositol 3-Kinases ; ErbB Receptors/genetics ; Female ; Gene Expression Profiling/methods ; Gene Ontology ; Humans ; Male ; Middle Aged ; Mutation ; Neoplasms/blood ; Neoplasms/diagnosis ; Neoplasms/genetics ; Pathology, Molecular/methods ; Phosphatidylinositol 3-Kinases/genetics ; Proto-Oncogene Proteins c-met/genetics ; Proto-Oncogene Proteins p21(ras)/genetics ; Receptor, ErbB-2/genetics ; Reproducibility of Results ; Sensitivity and Specificity ; Sequence Analysis, RNA/methods ; Signal Transduction/genetics ; Support Vector Machine ; Young Adult
Chemische Substanzen Biomarkers, Tumor ; KRAS protein, human ; Phosphatidylinositol 3-Kinases (EC 2.7.1.-) ; Class I Phosphatidylinositol 3-Kinases (EC 2.7.1.137) ; PIK3CA protein, human (EC 2.7.1.137) ; EGFR protein, human (EC 2.7.10.1) ; ErbB Receptors (EC 2.7.10.1) ; MET protein, human (EC 2.7.10.1) ; Proto-Oncogene Proteins c-met (EC 2.7.10.1) ; Receptor, ErbB-2 (EC 2.7.10.1) ; Proto-Oncogene Proteins p21(ras) (EC 3.6.5.2)
Sprache Englisch
Erscheinungsdatum 2015-10-29
Erscheinungsland United States
Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID 2078448-X
ISSN 1878-3686 ; 1535-6108
ISSN (online) 1878-3686
ISSN 1535-6108
DOI 10.1016/j.ccell.2015.09.018
Signatur
Zs.A 5650: Hefte anzeigen Standort:
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