2009
DOI: 10.1002/hed.21061
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Receptor tyrosine kinases in sinonasal undifferentiated carcinomas—Evaluation for EGFR, c‐KIT, and HER2/neu expression

Abstract: c-KIT is frequently expressed in SNUC. However, the overexpression is not due to activating mutations or gene amplification.

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Cited by 30 publications
(23 citation statements)
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References 45 publications
(39 reference statements)
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“…Novel therapies that have been attempted include boron neutron capture therapy [21], autologous bone marrow transplant [22], and neoadjuvant selective intra-arterial cisplatin with concurrent radiation therapy [23], both of which showed limited success. A recent histo-biochemical study of a small series of SNUC patients showed that these tumours have a strong expression c-KIT, which is a tyrosine kinase receptor typically expressed in gastrointestinal stromal tumours [24]. However, over-expression was not due to an activating mutation in the c-kit gene, and thus, the authors argued that use of TK-inhibitors targeting c-KIT (e.g.…”
Section: Discussionmentioning
confidence: 99%
“…Novel therapies that have been attempted include boron neutron capture therapy [21], autologous bone marrow transplant [22], and neoadjuvant selective intra-arterial cisplatin with concurrent radiation therapy [23], both of which showed limited success. A recent histo-biochemical study of a small series of SNUC patients showed that these tumours have a strong expression c-KIT, which is a tyrosine kinase receptor typically expressed in gastrointestinal stromal tumours [24]. However, over-expression was not due to an activating mutation in the c-kit gene, and thus, the authors argued that use of TK-inhibitors targeting c-KIT (e.g.…”
Section: Discussionmentioning
confidence: 99%
“…A nomogram to aid the decision process for or against adjuvant chemoradiation in oral squamous cell includes age, sex, surgical margin status, and tobacco use . Beyond these factors, biological features that reflect the aggressiveness of the disease have proven to be relevant . Exploring the function of different biomarkers offers the opportunity to move from a tumor model of temporal determinism to one of biological determinism, as carcinogenesis is not defined by what stage the patient is in at detection but rather by molecular characteristics of the tumor and the host.…”
Section: Discussionmentioning
confidence: 99%
“…There is a strong and diffuse expression of epithelial markers (AE1/AE3, CK7, OSCAR, CAM5.2, EMA; Figure 6), consistent p16 and CD117 reactions, and only focal, patchy nuclear reaction with p63, whereas CK5/6, p40, CEA, EBER, CD34, desmin, S100 protein, and calretinin are consistently negative. 53,[56][57][58][59][60][61] Focal, patchy, and/or weak reactions with neuroendocrine markers (NSE, synaptophysin, chromogranin, CD56) may be present, but there is no corresponding neuroendocrine morphology.…”
Section: Mesenchymal Chondrosarcomamentioning
confidence: 99%