1999
DOI: 10.3892/ijo.15.3.481
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Receptor for interleukin 13 is abundantly and specifically over-expressed in patients with glioblastoma multiforme.

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Cited by 50 publications
(54 citation statements)
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“…Interleukin 4 (IL4) and interleukin 13 (IL13) are two immune regulatory cytokines that can compete for binding to a heterodimeric cell surface receptor consisting of a 140-kDa IL4 receptor h subunit and a 45-kDa IL13 receptor a1 subunit (1). In contrast to most normal body tissues, high-grade gliomas can also bind IL13 in the presence of excess quantities of IL4, an effect referred to as IL4-independent IL13 binding (2)(3)(4)(5). The cell surface expression of a monomeric 42-kDa receptor capable of binding IL13 but not IL4, termed IL13 receptor a2 (IL13Ra2), was used to explain this effect (6).…”
Section: Introductionmentioning
confidence: 99%
“…Interleukin 4 (IL4) and interleukin 13 (IL13) are two immune regulatory cytokines that can compete for binding to a heterodimeric cell surface receptor consisting of a 140-kDa IL4 receptor h subunit and a 45-kDa IL13 receptor a1 subunit (1). In contrast to most normal body tissues, high-grade gliomas can also bind IL13 in the presence of excess quantities of IL4, an effect referred to as IL4-independent IL13 binding (2)(3)(4)(5). The cell surface expression of a monomeric 42-kDa receptor capable of binding IL13 but not IL4, termed IL13 receptor a2 (IL13Ra2), was used to explain this effect (6).…”
Section: Introductionmentioning
confidence: 99%
“…Data have been published indicating that the EGF receptor expression is low or absent in normal human brain tissue. [17][18][19] Other investigators have found EGF receptor expression in various cell types in the normal human brain, although not in glial cells. 20,21 Therefore, before a phase I clinical trial with 425.3-PE can be initiated, its toxicology profile may need to be determined in species other than rat or mice.…”
Section: Immunotoxin Treatment Of Xenografted Human Gliomas In Nude Rmentioning
confidence: 99%
“…Our laboratory and subsequent independent investigations have consistently demonstrated that IL13R␣2 is overexpressed in a vast majority (ϳ80%) of HGA cells in vitro and in vivo, [8][9][10][11][12][13] making it an attractive target for antiglioma molecular therapy. The potential of utilizing IL13R␣2 as a cancer target has been demonstrated by using a number of distinct delivery strategies.…”
Section: Introductionmentioning
confidence: 99%