Literature DB >> 16530697

High-grade glioma: can we teach an old dogma new tricks?

Richard J Gilbertson1.   

Abstract

The best efforts of clinicians and biologists battling high-grade glioma (HGG) have been overshadowed by two cruel facts: these tumors are essentially incurable and will kill most patients within months, and emergent knowledge of the genetic alterations in HGG has done nothing to ease this burden of suffering. In this issue of Cancer Cell, Phillips et al. report an extensive study of the gene expression profiles of a large cohort of HGG. Their data provide new clues to the origins of this disease and suggest potential targets for novel therapies.

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Year:  2006        PMID: 16530697     DOI: 10.1016/j.ccr.2006.02.024

Source DB:  PubMed          Journal:  Cancer Cell        ISSN: 1535-6108            Impact factor:   31.743


  3 in total

1.  Inhibition of sphingosine kinase 1 suppresses proliferation of glioma cells under hypoxia by attenuating activity of extracellular signal-regulated kinase.

Authors:  H Zhang; W Li; S Sun; S Yu; M Zhang; F Zou
Journal:  Cell Prolif       Date:  2012-01-30       Impact factor: 6.831

2.  Differential expression of p42.3 in low- and high-grade gliomas.

Authors:  Weiqing Wan; Xiaoqing Xu; Guijun Jia; Wenmei Li; Junmei Wang; Tong Ren; Zhen Wu; Junting Zhang; Liwei Zhang; Youyong Lu
Journal:  World J Surg Oncol       Date:  2014-06-14       Impact factor: 2.754

3.  Up-regulation of ANKDR49, a poor prognostic factor, regulates cell proliferation of gliomas.

Authors:  Chunyan Hao; Hubin Duan; Hao Li; Mingyang Pei; Yueting Liu; Yimin Fan; Ce Zhang
Journal:  Biosci Rep       Date:  2017-08-04       Impact factor: 3.840

  3 in total

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