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西妥昔单抗和顺铂通过使表皮生长因子受体/蛋白激酶B信号通路失活,在鼻咽癌细胞系中显示出不同的联合效应。

Cetuximab and Cisplatin Show Different Combination Effect in Nasopharyngeal Carcinoma Cells Lines via Inactivation of EGFR/AKT Signaling Pathway.

作者信息

Gu Jiajia, Yin Li, Wu Jing, Zhang Nan, Huang Teng, Ding Kai, Cao Haixia, Xu Lin, He Xia

机构信息

The Fourth Clinical School of Nanjing Medical University, Nanjing 210009, China; Department of Radiation Oncology, Nanjing Medical University Affiliated Jiangsu Cancer Hospital and Jiangsu Institute of Cancer Research, Nanjing 210009, China; Jiangsu Key Laboratory of Molecular and Translational Cancer Research, Nanjing, China.

Department of Radiation Oncology, Nanjing Medical University Affiliated Jiangsu Cancer Hospital and Jiangsu Institute of Cancer Research, Nanjing 210009, China.

出版信息

Biochem Res Int. 2016;2016:7016907. doi: 10.1155/2016/7016907. Epub 2016 May 24.

Abstract

Nasopharyngeal carcinoma (NPC) is a common malignant cancer in South China. Cisplatin is a classical chemotherapeutic employed for NPC treatment. Despite the use of cisplatin-based concurrent chemoradiotherapy, distant failure still confuses clinicians and the outcome of metastatic NPC remains disappointing. Hence, a potent systemic therapy is needed for this cancer. Epidermal growth factor receptor (EGFR) represents a promising new therapeutic target in cancer. We predicted that combining the conventional cytotoxic drug cisplatin with the novel molecular-targeted agent cetuximab demonstrates a strong antitumor effect on NPC cells. In this study, we selected HNE1 and CNE2 cells, which have been proved to possess different EGFR expression levels, to validate our conjecture. The two-drug regimen showed a significant synergistic effect in HNE1 cells but an additive effect in CNE2 cells. Our results showed that cisplatin-induced apoptosis was significantly enhanced by cetuximab in the high EGFR-expressing HNE1 cells but not in CNE2 cells. Further molecular mechanism study indicated that the EGFR/AKT pathway may play an important role in cell apoptosis via the mitochondrial-mediated intrinsic pathway and lead to the different antitumor effects of this two-drug regimen between HNE1 and CNE2 cells. Thus, the regimen may be applied in personalized NPC treatments.

摘要

鼻咽癌(NPC)是中国南方常见的恶性肿瘤。顺铂是用于鼻咽癌治疗的经典化疗药物。尽管采用了基于顺铂的同步放化疗,但远处转移仍困扰着临床医生,转移性鼻咽癌的治疗效果仍然令人失望。因此,这种癌症需要一种有效的全身治疗方法。表皮生长因子受体(EGFR)是癌症中一个有前景的新治疗靶点。我们预测,将传统细胞毒性药物顺铂与新型分子靶向药物西妥昔单抗联合使用,对鼻咽癌细胞具有强大的抗肿瘤作用。在本研究中,我们选择了已被证明具有不同EGFR表达水平的HNE1和CNE2细胞,以验证我们的推测。两药联合方案在HNE1细胞中显示出显著的协同作用,而在CNE2细胞中显示出相加作用。我们的结果表明,西妥昔单抗在高表达EGFR的HNE1细胞中显著增强了顺铂诱导的细胞凋亡,但在CNE2细胞中未增强。进一步的分子机制研究表明,EGFR/AKT通路可能通过线粒体介导的内源性途径在细胞凋亡中起重要作用,并导致该两药联合方案在HNE1和CNE2细胞之间产生不同的抗肿瘤效果。因此,该联合方案可应用于鼻咽癌的个体化治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8237/4894995/75916cf29e0d/BRI2016-7016907.001.jpg

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