2012
DOI: 10.1016/j.ijrobp.2010.08.036
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High-Grade Glioma Relationship to the Neural Stem Cell Compartment: A Retrospective Review of 104 Cases

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Cited by 11 publications
(6 citation statements)
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“…First, the relatively small number of patients with grade IV astrocytomas and the fact that we combined the data for astrocytoma grades I and II, and grades III and IV might have affected the grade-specific patient-based SVZ-contact rates. However, the increase in SVZ-contact rates with increasing WHO grade of gliomas was reasonable in theory, and in agreement with previous reports [ 19 , 27 , 39 ]. Second, not all SCMs were pathologically verified.…”
Section: Discussionsupporting
confidence: 93%
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“…First, the relatively small number of patients with grade IV astrocytomas and the fact that we combined the data for astrocytoma grades I and II, and grades III and IV might have affected the grade-specific patient-based SVZ-contact rates. However, the increase in SVZ-contact rates with increasing WHO grade of gliomas was reasonable in theory, and in agreement with previous reports [ 19 , 27 , 39 ]. Second, not all SCMs were pathologically verified.…”
Section: Discussionsupporting
confidence: 93%
“…These findings suggested that the SVZ is intimately associated with the occurrence and development of gliomas. The overall SVZ-contact rate for astrocytomas was 75.2% in our study, which is lower than the rates reported by Barami et al [ 19 ] and Marsh et al [ 27 ]. There are several potential explanations for the difference between the above studies and ours.…”
Section: Discussioncontrasting
confidence: 85%
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“…The hypothesis is based on previous preclinical and clinical research which showed that the SVZ might support the growth of LGG and HGG by providing the tumor with NSCs. 5–7 , 14 , 41 However, it remains controversial, as there is a limited number of previous studies that in contrast report that irradiation of the SVZ decreases OS for patients with HGG. 42–45 A preclinical study by Achanta et al reported a decrease of the proliferating cell marker Ki67 in a mouse model when the SVZ was irradiated, 46 indicating a deteriorated repair capacity.…”
Section: Discussionmentioning
confidence: 99%
“…The hypothesis is based on previous pre-clinical and clinical research which showed that the SVZ might support the growth of LGG and HGG by providing the tumor with NSCs. [5][6][7][8]39 However, it remains controversial, as there is a limited number of previous studies that in contrast report that irradiation of the SVZ decreases OS for patients with HGG. [40][41][42][43] A preclinical study by Achanta et al reported a decrease of the proliferating cell marker Ki67 in a mouse model when the SVZ was irradiated, 44 41,42 Our study describes this negative correlation between SVZ irradiation and OS in HGG patients as well, involving a large number of patients (n = 226).…”
Section: Discussionmentioning
confidence: 99%