論文

査読有り 国際誌
2018年9月10日

Anti-EGFR antibody cetuximab is secreted by oral squamous cell carcinoma and alters EGF-driven mesenchymal transition.

Biochemical and biophysical research communications
  • Toshifumi Fujiwara
  • ,
  • Takanori Eguchi
  • ,
  • Chiharu Sogawa
  • ,
  • Kisho Ono
  • ,
  • Jun Murakami
  • ,
  • Soichiro Ibaragi
  • ,
  • Jun-Ichi Asaumi
  • ,
  • Kuniaki Okamoto
  • ,
  • Stuart K Calderwood
  • ,
  • Ken-Ichi Kozaki

503
3
開始ページ
1267
終了ページ
1272
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.bbrc.2018.07.035

Genetic amplification, overexpression, and increased signaling from the epidermal growth factor receptor (EGFR) are often found in oral squamous cell carcinoma (OSCC) and thus EGFR is frequently targeted molecularly by the therapeutic antibody cetuximab. We assessed effects of cetuximab in control of EGF-driven malignant traits of OSCC cells. EGF stimulation promoted progression level of mesenchymal traits in OSCC cells, which were attenuated by cetuximab but incompletely. We pursued a potential mechanism underlying such incomplete attenuation of OSCC malignant traits. Cetuximab promoted secretion of EGFR-EVs by OSCC cells and failed to inhibit EGF-driven secretion of EGFR-EVs. Cetuximab was also found to be robustly secreted with the EGFR-EVs by the OSCC cells. Thus, EGF promotes the level of mesenchymal traits of OSCC cells and secretion of EGFR-EVs, which involve cetuximab resistance.

リンク情報
DOI
https://doi.org/10.1016/j.bbrc.2018.07.035
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30017201
ID情報
  • DOI : 10.1016/j.bbrc.2018.07.035
  • PubMed ID : 30017201

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