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Sökning: WFRF:(Wiles C) > (2010-2014)

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1.
  • Glover, Katherine C., et al. (författare)
  • Deglaciation, basin formation and post-glacial climate change from a regional network of sediment core sites in Ohio and eastern Indiana
  • 2011
  • Ingår i: Quaternary Research. - : Cambridge University Press (CUP). - 0033-5894 .- 1096-0287. ; 76:3, s. 401-410
  • Tidskriftsartikel (refereegranskat)abstract
    • Many paleoclimate and landscape change studies in the American Midwest have focused on the Gate Glacial and early Holocene time periods (similar to 16-11 ka), but little work has addressed landscape change in this area between the Last Glacial Maximum and the Late Glacial (similar to 22-16 ka). Sediment cores were collected from 29 new lake and bog sites in Ohio and Indiana to address this gap. The basal radiocarbon dates from these cores show that initial ice retreat from the maximal last-glacial ice extent occurred by 22 ka, and numerous sites that are similar to 100 km inside this limit were exposed by 18.9 ka. Post-glacial environmental changes were identified as stratigraphic or biologic changes in select cores. The strongest signal occurs between 18.5 and 14.6 ka. These Midwestern events correspond with evidence to the northeast, suggesting that initial deglaciation of the ice sheet, and ensuing environmental changes, were episodic and rapid. Significantly, these changes predate the onset of the Belling postglacial warming (14.8 ka) as recorded by the Greenland ice cores. Thus, deglaciation and landscape change around the southern margins of the Laurentide Ice Sheet happened similar to 7 ka before postglacial changes were felt in central Greenland. (C) 2011 University of Washington.
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2.
  • Hung, Noelyn, et al. (författare)
  • Increased paired box transcription factor 8 has a survival function in Glioma
  • 2014
  • Ingår i: BMC Cancer. - : Springer Science and Business Media LLC. - 1471-2407 .- 1471-2407. ; 14, s. 159-
  • Tidskriftsartikel (refereegranskat)abstract
    • Background:The molecular basis to overcome therapeutic resistance to treat glioblastoma remains unclear. The anti-apoptotic b cell lymphoma 2 (BCL2) gene is associated with treatment resistance, and is transactivated by the paired box transcription factor 8 (PAX8). In earlier studies, we demonstrated that increased PAX8 expression in glioma cell lines was associated with the expression of telomerase. In this current study, we more extensively explored a role for PAX8 in gliomagenesis.Methods:PAX8 expression was measured in 156 gliomas including telomerase-negative tumours, those with the alternative lengthening of telomeres (ALT) mechanism or with a non-defined telomere maintenance mechanism (NDTMM), using immunohistochemistry and quantitative PCR. We also tested the affect of PAX8 knockdown using siRNA in cell lines on cell survival and BCL2 expression.Results:Seventy-two percent of glioblastomas were PAX8-positive (80% telomerase, 73% NDTMM, and 44% ALT). The majority of the low-grade gliomas and normal brain cells were PAX8-negative. The suppression of PAX8 was associated with a reduction in both cell growth and BCL2, suggesting that a reduction in PAX8 expression would sensitise tumours to cell death.Conclusions:PAX8 is increased in the majority of glioblastomas and promoted cell survival. Because PAX8 is absent in normal brain tissue, it may be a promising therapeutic target pathway for treating aggressive gliomas.
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