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10.1126/scitranslmed.aaa7582

http://scihub22266oqcxt.onion/10.1126/scitranslmed.aaa7582
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suck abstract from ncbi


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pmid26333934      Sci+Transl+Med 2015 ; 7 (303): 303ra138
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  • Magnetic resonance image features identify glioblastoma phenotypic subtypes with distinct molecular pathway activities #MMPMID26333934
  • Itakura H; Achrol AS; Mitchell LA; Loya JJ; Liu T; Westbroek EM; Feroze AH; Rodriguez S; Echegaray S; Azad TD; Yeom KW; Napel S; Rubin DL; Chang SD; Harsh GR; Gevaert O
  • Sci Transl Med 2015[Sep]; 7 (303): 303ra138 PMID26333934show ga
  • Glioblastoma (GBM) is the most common and highly lethal primary malignant brain tumor in adults. There is a dire need for easily accessible, noninvasive biomarkers that can delineate underlying molecular activities and predict response to therapy. To this end, we sought to identify subtypes of GBM, differentiated solely by quantitative MR imaging features, that could be used for better management of GBM patients. Quantitative image features capturing the shape, texture, and edge sharpness of each lesion were extracted from MR images of 121 patients with de novo, solitary, unilateral GBM. Three distinct phenotypic ?clusters? emerged in the development cohort using consensus clustering with 10,000 iterations on these image features. These three clusters?pre-multifocal, spherical, and rim-enhancing, names reflecting their image features?were validated in an independent cohort consisting of 144 multi-institution patients with similar tumor characteristics from The Cancer Genome Atlas (TCGA). Each cluster mapped to a unique set of molecular signaling pathways using pathway activity estimates derived from analysis of TCGA tumor copy number and gene expression data with the PARADIGM algorithm. Distinct pathways, such as c-Kit and FOXA, were enriched in each cluster, indicating differential molecular activities as determined by image features. Each cluster also demonstrated differential probabilities of survival, indicating prognostic importance. Our imaging method offers a noninvasive approach to stratify GBM patients and also provides unique sets of molecular signatures to inform targeted therapy and personalized treatment of GBM.
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