Predictive and prognostic value of human copper transporter 1 (hCtr1) in patients with stage III non-small-cell lung cancer receiving first-line platinum-based doublet chemotherapy.
Predictive and prognostic value of human copper transporter 1 (hCtr1) in patients with stage III non-small-cell lung cancer receiving first-line platinum-based doublet chemotherapy.
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DOI:
10.1016/j.lungcan.2011.06.011
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发表时间:
2012-02
期刊:
影响因子:
5.3
通讯作者:
Su, Wu-Chou
中科院分区:
文献类型:
--
作者:
Chen, Helen H. W.;Yan, Jiang-Jou;Chen, Wen-Chung;Kuo, Macus Tien;Lai, Yu-Hsuan;Lai, Wu-Wei;Liu, Hsiao-Sheng;Su, Wu-Chou
Recent studies have shown that human copper transporter 1 (hCtr1), the major copper influx transporter, is involved in the transport of platinum-based antitumor agents. We investigated the predictive and prognostic values of hCtr1, and cooper efflux transporters ATP7A and ATP7B, in patients with locally advanced non-small cell lung cancer (NSCLC) receiving first-line platinum-based chemotherapy. From 2004 to 2009, we identified 54 consecutive stage III NSCLC patients who underwent first-line platinum-based doublet chemotherapy. Immunohistochemical studies of hCtr1, ATP7A and ATP7B on the paraffin-embedded pre-treatment tumor samples were performed and correlated with chemotherapy response and survival. Overexpression of hCtr1, ATP7A and ATP7B were observed in 68%, 48% and 74% of the participants, respectively. hCtr1 overexpression was associated with better chemotherapy responses (P < 0.01); whereas ATP7A and ATP7B were not. Patients with hCtr1 overexpressing tumors had better progression-free survival (PFS) and overall survival (OS) (P = 0.01 and 0.047, respectively). In multivariate analyses for chemotherapy response and PFS, only hCtr1 overexpression emerged as a favorable independent predictive and prognostic factor (all P < 0.01). This is the first report to state that hCtr1 is not only an independent predictor of platinum-based chemotherapy response but also a prognostic factor in stage III NSCLC.
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DOI:
10.1158/1078-0432.ccr-09-0311
发表时间:
2009-07-01
期刊:
Clinical cancer research : an official journal of the American Association for Cancer Research
影响因子:
--
作者:
Blair BG;Larson CA;Safaei R;Howell SB
通讯作者:
Howell SB
影响因子:
3.6
作者:
Chen, Helen H. W.;Song, Im-Sook;Kuo, Macus Tien
通讯作者:
Kuo, Macus Tien
影响因子:
4.8
作者:
Leonhardt, Karoline;Gebhardt, Rolf;Huster, Dominik
通讯作者:
Huster, Dominik
影响因子:
45.3
作者:
Fossella, F;Pereira, JR;Belani, CP
通讯作者:
Belani, CP
影响因子:
4.8
作者:
Miyashita, H;Nitta, Y;Takebayashi, Y
通讯作者:
Takebayashi, Y