Literature DB >> 24626880

Cetuximab-mediated ADCC activity is correlated with the cell surface expression level of EGFR but not with the KRAS/BRAF mutational status in colorectal cancer.

Yuki Seo1, Yoshiyuki Ishii1, Hiroki Ochiai1, Kazumasa Fukuda1, Shingo Akimoto1, Tetsu Hayashida1, Koji Okabayashi1, Masashi Tsuruta1, Hirotoshi Hasegawa1, Yuko Kitagawa1.   

Abstract

Cetuximab, an IgG1 monoclonal antibody against the epidermal growth factor receptor (EGFR), is widely used for the treatment of metastatic colorectal cancer (mCRC). One of the mechanisms of action is considered to be antibody-dependent cell-mediated cytotoxicity (ADCC) triggered by Fcγ-R on natural killer cells. However, whether ADCC is associated with EGFR expression and/or the mutational status of EGF downstream effectors (KRAS and BRAF) in colorectal cancer (CRC) remains unclear. The aim of the present study was to verify whether ADCC activities are associated with the cell surface expression levels of EGFR and/or the mutational status of KRAS and BRAF. Five human CRC cell lines with different cell surface expression levels of EGFR and different KRAS and BRAF mutational statuses were selected to evaluate ADCC activity using peripheral blood mononuclear cells (PBMCs) from healthy human donors. Furthermore, tumor cells from resected specimens of CRC patients were used to evaluate the cell surface expression level of EGFR using immunohistochemistry and the KRAS and BRAF mutational statuses using direct sequencing, while the ADCC activity was examined using PBMCs from the same CRC patients. A strong correlation was observed between the expression levels of EGFR and the ADCC activities in the cell lines (correlation coefficient: 0.949; P=0.003). Of the 13 resected specimens, a high ADCC activity level was significantly observed in tumor cells with high expression levels of cell surface EGFR, when compared with that in the tumor cells with low expression levels (P=0.027). In both CRC cell lines and tumor cells from CRC patients, the ADCC activities were significantly associated with the cell surface expression levels of EGFR [standard partial regression coefficients: 0.911 (P=0.017) and 0.660 (P=0.018), respectively], but not with the mutational status of KRAS and BRAF [standard partial regression coefficient: -0.101 (P=0.631) and 0.160 (P=0.510), respectively]. Cetuximab-mediated ADCC activity may be correlated with the cell surface expression level of EGFR, regardless of the mutational statuses of KRAS and BRAF, in CRC.

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Year:  2014        PMID: 24626880     DOI: 10.3892/or.2014.3077

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  24 in total

1.  Evaluation of antibody-dependent cell-mediated cytotoxicity activity and cetuximab response in KRAS wild-type metastatic colorectal cancer patients.

Authors:  Cristiana Lo Nigro; Vincenzo Ricci; Daniela Vivenza; Martino Monteverde; Giuliana Strola; Francesco Lucio; Federica Tonissi; Emanuela Miraglio; Cristina Granetto; Mirella Fortunato; Marco Carlo Merlano
Journal:  World J Gastrointest Oncol       Date:  2016-02-15

Review 2.  Prognostic and predictive biomarkers in metastatic colorectal cancer anti-EGFR therapy.

Authors:  Cristiana Lo Nigro; Vincenzo Ricci; Daniela Vivenza; Cristina Granetto; Teresa Fabozzi; Emanuela Miraglio; Marco C Merlano
Journal:  World J Gastroenterol       Date:  2016-08-14       Impact factor: 5.742

3.  Targeting secondary immune responses to cetuximab: CD137 and the outside story.

Authors:  Julie E Bauman; Jennifer R Grandis
Journal:  J Clin Invest       Date:  2014-05-16       Impact factor: 14.808

4.  Resistance to obinutuzumab-induced antibody-dependent cellular cytotoxicity caused by abnormal Fas signaling is overcome by combination therapies.

Authors:  Natsumi Kawasaki; Yoriko Yamashita-Kashima; Takaaki Fujimura; Shigeki Yoshiura; Naoki Harada; Osamu Kondoh; Yasushi Yoshimura
Journal:  Mol Biol Rep       Date:  2022-02-26       Impact factor: 2.742

5.  Efficacy of aerosol therapy of lung cancer correlates with EGFR paralysis induced by AvidinOX-anchored biotinylated Cetuximab.

Authors:  Rita De Santis; Antonio Rosi; Anna Maria Anastasi; Caterina Chiapparino; Claudio Albertoni; Barbara Leoni; Angela Pelliccia; Daniela Santapaola; Valeria Carollo; Emanuele Marra; Luigi Aurisicchio; Brunilde Arseni; Maria Lucrezia Pacello; Gabriella Palmieri; Simone Battella; Fiorella Petronzelli; Ferdinando Maria Milazzo
Journal:  Oncotarget       Date:  2014-10-15

6.  Cetuximab intensifies the ADCC activity of adoptive NK cells in a nude mouse colorectal cancer xenograft model.

Authors:  Shanshan Chen; Xuechun Li; Rongming Chen; Mingang Yin; Qiuhong Zheng
Journal:  Oncol Lett       Date:  2016-07-11       Impact factor: 2.967

Review 7.  Recent Advances in Targeting the EGFR Signaling Pathway for the Treatment of Metastatic Colorectal Cancer.

Authors:  Yuji Miyamoto; Koichi Suyama; Hideo Baba
Journal:  Int J Mol Sci       Date:  2017-04-02       Impact factor: 5.923

8.  Expression of the chemokine CXCL14 and cetuximab-dependent tumour suppression in head and neck squamous cell carcinoma.

Authors:  T Kondo; S Ozawa; T Ikoma; X-Y Yang; K Kanamori; K Suzuki; H Iwabuchi; Y Maehata; C Miyamoto; T Taguchi; T Kiyono; E Kubota; R-I Hata
Journal:  Oncogenesis       Date:  2016-07-11       Impact factor: 7.485

9.  The impact of co-expression of wild-type EGFR and its ligands determined by immunohistochemistry for response to treatment with cetuximab in patients with metastatic colorectal cancer.

Authors:  Said Khelwatty; Sharadah Essapen; Izhar Bagwan; Margaret Green; Alan Seddon; Helmout Modjtahedi
Journal:  Oncotarget       Date:  2017-01-31

10.  Combined Effect of Anti-SSEA4 and Anti-Globo H Antibodies on Breast Cancer Cells.

Authors:  Ruey-Herng Lee; Yu-Jen Wang; Ting-Yen Lai; Tsui-Ling Hsu; Po-Kai Chuang; Han-Chung Wu; Chi-Huey Wong
Journal:  ACS Chem Biol       Date:  2021-08-09       Impact factor: 4.634

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