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Epidermal Growth Factor Receptor and its Oncogenic EGFRvIII Variant in Benign and Malignant Brain Tumors.
Kielbus, Michal; Rola, Radoslaw; Jarosz, Bozena; Jeleniewicz, Witold; Cybulski, Marek; Stenzel-Bembenek, Agnieszka; Podkowinski, Arkadiusz; Smok-Kalwat, Jolanta; Polberg, Krzysztof; Trojanowski, Tomasz; Stefaniuk, Dawid; Stepulak, Andrzej.
Afiliação
  • Kielbus M; Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland; michal.kielbus@umlub.pl.
  • Rola R; Department of Neurosurgery and Pediatric Neurosurgery, Medical University of Lublin, Lublin, Poland.
  • Jarosz B; Department of Neurosurgery and Pediatric Neurosurgery, Medical University of Lublin, Lublin, Poland.
  • Jeleniewicz W; Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
  • Cybulski M; Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
  • Stenzel-Bembenek A; Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
  • Podkowinski A; Department of Neurosurgery and Pediatric Neurosurgery, Medical University of Lublin, Lublin, Poland.
  • Smok-Kalwat J; Clinic of Clinical Oncology, Holycross Cancer Centre, Kielce, Poland.
  • Polberg K; Department of Otolaryngology, MSWiA Hospital, Lublin, Poland.
  • Trojanowski T; Department of Neurosurgery and Pediatric Neurosurgery, Medical University of Lublin, Lublin, Poland.
  • Stefaniuk D; Chair of Biochemistry and Biotechnology, Faculty of Biology and Biotechnology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Lublin, Poland.
  • Stepulak A; Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
Anticancer Res ; 41(2): 983-991, 2021 Feb.
Article em En | MEDLINE | ID: mdl-33517305
ABSTRACT
BACKGROUND/

AIM:

Tumorigenesis and cancer progression might be driven by abnormal activation of growth factor receptors. Importantly, molecular changes in EGFR-dependent signaling is one of the most common characteristics of brain tumors. PATIENTS AND

METHODS:

HER1 and EGFRvIII variants in meningiomas and glioblastomas were evaluated at the RNA level.

RESULTS:

EGFRvIII was found in 18.6% of glioblastomas (GBM), whereas 25% of EGFRvIII positive tumors express wild-type EGFR as well. HER1 was over-expressed in benign meningiomas compared to glioblastomas, whereas HER1 expression in meningiomas differed significantly between sub-types of meningiomas. EGFRvIII and HER1 where positively correlated in glioblastomas. Yet, the patient overall survival did not differ between high- and low-HER1 expressing glioblastomas or between EGFRvIII positive and negative GBMs.

CONCLUSION:

HER1 may be considered as an independent factor for classification of benign meningiomas. The mRNA levels of HER1 or EGFRvIII should not be used as independent prognostic factors for patients with gliomas.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Neoplasias Meníngeas / Meningioma / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Neoplasias Meníngeas / Meningioma / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article