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CXCL8在结直肠癌中过表达,增强了结直肠癌细胞对失巢凋亡的抗性。

CXCL8, overexpressed in colorectal cancer, enhances the resistance of colorectal cancer cells to anoikis.

作者信息

Xiao You-Chuan, Yang Zhi-Bin, Cheng Xian-Shuo, Fang Xing-Bao, Shen Tao, Xia Cui-Feng, Liu Ping, Qian Hai-Hua, Sun Bin, Yin Zheng-Feng, Li Yun-Feng

机构信息

Colorectal Cancer Clinical Research Center, Third Affiliated Hospital, Kunming Medical University, Kunming 650118, China; Molecular Oncology Laboratory, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China; Medical Oncology, First People's Hospital of Qujing, Qujing 655000, China.

Colorectal Cancer Clinical Research Center, Third Affiliated Hospital, Kunming Medical University, Kunming 650118, China.

出版信息

Cancer Lett. 2015 May 28;361(1):22-32. doi: 10.1016/j.canlet.2015.02.021. Epub 2015 Feb 14.

Abstract

Anoikis is a form of apoptosis which occurs when anchorage-dependent cells either show loss of adhesion or inappropriate adhesion. Only a few cancer cells that detach from the primary site of the tumor acquire the ability to resist anoikis and form metastasis. The mechanism underlying the resistance of colorectal cancer (CRC) cells to anoikis remains unclear. Interleukin-8 (alternatively known as CXCL8) is associated with CRC angiogenesis and progression. Here, we found that a high abundance of CXCL8 or TOPK strongly correlated with poor overall and disease-free survival of 186 patients with CRC. A combination of high CXCL8 and high TOPK expressions had the worst prognosis. We showed that CXCL8 expression was negatively correlated with anoikis in CRC cells. CXCL8 treatment enhanced the resistance of CRC cells to apoptosis, which was accompanied by the increase of TOPK, and the activation of AKT and ERK. Moreover, we demonstrated that the inhibition of either ERK or AKT by specific chemical inhibitors attenuated the CXCL8-mediated resistance to anoikis. Treatment with AKT inhibitor abolished the effects of CXCL8 on TOPK expression, suggesting that TOPK was downstream of AKT in the process of anoikis. Taken together, we demonstrated that CXCL8 is strongly implicated in the resistance of CRC cells to anoikis, and that the AKT, TOPK and ERK pathway may be a potential therapeutic target for CRC.

摘要

失巢凋亡是一种细胞凋亡形式,当锚定依赖性细胞出现黏附丧失或黏附不当的情况时就会发生。只有少数从肿瘤原发部位脱离的癌细胞获得抵抗失巢凋亡并形成转移的能力。结直肠癌(CRC)细胞抵抗失巢凋亡的机制仍不清楚。白细胞介素-8(也称为CXCL8)与CRC血管生成和进展相关。在此,我们发现186例CRC患者中,高丰度的CXCL8或TOPK与较差的总生存期和无病生存期密切相关。CXCL8高表达和TOPK高表达共同出现时预后最差。我们发现CRC细胞中CXCL8表达与失巢凋亡呈负相关。CXCL8处理增强了CRC细胞对凋亡抵抗,这伴随着TOPK增加以及AKT和ERK激活。此外,我们证明用特异性化学抑制剂抑制ERK或AKT可减弱CXCL8介导的对失巢凋亡的抵抗。用AKT抑制剂处理消除了CXCL8对TOPK表达的影响,表明在失巢凋亡过程中TOPK位于AKT下游。综上所述,我们证明CXCL8与CRC细胞对失巢凋亡的抵抗密切相关,且AKT、TOPK和ERK通路可能是CRC的潜在治疗靶点。

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