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Sökning: id:"swepub:oai:DiVA.org:liu-133696" > EGFR protein overex...

EGFR protein overexpression and gene copy number increases in oral tongue squamous cell carcinoma.

Ryott, Michael (författare)
Karolinska Institutet
Wangsa, Darawalee (författare)
Department of Oncology-Pathology, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden. Genetics Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Building 50, Bethesda, MD, USA.
Heselmeyer-Haddad, Kerstin (författare)
Genetics Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Building 50, Bethesda, MD, USA
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Lindholm, Johan (författare)
Department of Oncology-Pathology, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden
Elmberger, Göran (författare)
Karolinska Institutet
Auer, Gert (författare)
Karolinska Institutet
Åvall Lundqvist, Elisabeth (författare)
Karolinska Institutet
Ried, Thomas (författare)
Genetics Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Building 50, Bethesda, MD, USA
Munck-Wikland, Eva (författare)
Karolinska Institutet
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Karolinska Institutet Department of Oncology-Pathology, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden Genetics Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Building 50, Bethesda, MD, USA. (creator_code:org_t)
Pergamon Press, 2009
2009
Engelska.
Ingår i: European Journal of Cancer. - : Pergamon Press. - 0959-8049 .- 1879-0852. ; 45:9, s. 1700-1708
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • New promising therapeutic agents targeting epidermal growth factor receptor (EGFR) have been developed although clinical information concerning EGFR status in oral tongue squamous cell carcinoma (OTSCC) is limited. We investigated EGFR protein expression and gene copy numbers in 78 pretreatment OTSCC paraffin samples. EGFR protein expression was found in all 78 tumours, of which 72% showed an intense staining. Fifty-four percent of the tumours had high (> or =four gene copies) EGFR gene copy numbers. EGFR gene copy number was significantly associated with EGFR protein expression (P=0.002). Pretreatment EGFR staining intensity tended to be associated with non-pathological complete remission after preoperative radiotherapy for Stage II OTSCC. No correlation was found between EGFR status and survival. EGFR FISH results were significantly (P=0.003) higher in more advanced tumours (Stages II, III and IV) than in the tumours in Stage I. Non-smokers exhibited a significantly higher EGFR gene copy number and protein overexpression in Stages I and II OTSCC than smokers (P=0.001, P=0.009). In conclusion, EGFR was found to be overexpressed in all OTSCCs making this cancer type interesting for exploring new therapeutic agents targeting the EGFR receptor.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Mouth neoplasms
In situ hybridisation
Fluorescence
Immunohistochemistry

Publikations- och innehållstyp

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