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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
被引:49
作者:

Seo, Yuki
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Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan

Ishii, Yoshiyuki
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Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan

Ochiai, Hiroki
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Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan

Fukuda, Kazumasa
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Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan

Akimoto, Shingo
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Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan

Hayashida, Tetsu
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Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan

Okabayashi, Koji
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Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan

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[1] Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan
关键词:
colorectal cancer;
epidermal growth factor receptor;
cell surface expression;
cetuximab;
antibody-dependent cell-mediated cytotoxicity;
GROWTH-FACTOR RECEPTOR;
ANTITUMOR-ACTIVITY;
WILD-TYPE;
COLON;
CYTOTOXICITY;
SURVIVAL;
LINES;
D O I:
10.3892/or.2014.3077
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
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 Fc gamma-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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页码:2115 / 2122
页数:8
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机构: Tottori Univ, Fac Med, Dept Multidisciplinary Internal Med, Div Med Oncol & Mol Respirol, Yonago, Tottori 6838504, Japan

Yamaguchi, Kosuke
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Yamasaki, Akira
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Sako, Takanori
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Touge, Hirokazu
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Makino, Haruhiko
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Takata, Miyako
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Miyata, Masanori
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Nakamoto, Masaki
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Burioka, Naoto
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Shimizu, Eiji
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[10]
Correlation of pharmacokinetics with the antitumor activity of Cetuximab in nude mice bearing the GEO human colon carcinoma xenograft
[J].
Luo, FR
;
Yang, Z
;
Dong, H
;
Camuso, A
;
McGlinchey, K
;
Fager, K
;
Flefleh, C
;
Kan, D
;
Inigo, I
;
Castaneda, S
;
Rose, WC
;
Kramer, RA
;
Wild, R
;
Lee, FY
.
CANCER CHEMOTHERAPY AND PHARMACOLOGY,
2005, 56 (05)
:455-464

Luo, FR
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h-index: 0
机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Yang, Z
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Dong, H
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h-index: 0
机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Camuso, A
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h-index: 0
机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

McGlinchey, K
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h-index: 0
机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Fager, K
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Flefleh, C
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Kan, D
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Inigo, I
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Castaneda, S
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Rose, WC
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Kramer, RA
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Wild, R
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA

Lee, FY
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机构: Bristol Myers Squibb Co, Pharmaceut Res Inst, Oncol Drug Discovery, Princeton, NJ 08543 USA