Expression of cytoskeleton-associated protein 4 is associated with poor prognosis and metastasis in nasopharyngeal carcinoma

被引:2
|
作者
Cai, Manbo [1 ]
Wu, Weijun [1 ]
Deng, Shengling [2 ]
Yang, Qiao [1 ]
Wu, Haibiao [1 ]
Wang, Haiyun [3 ]
Zhang, Jiaxing [3 ]
Feng, Qisheng [3 ]
Shao, Jianyong [3 ]
Zeng, Yixin [3 ]
Li, Jianjun [4 ]
机构
[1] Univ South China, Affiliated Hosp 1, Hengyang Med Sch, Dept Radiotherapy, Hengyang 421001, Peoples R China
[2] Univ South China, Affiliated Hosp 2, Hengyang Med Sch, Dept Anesthesia, Hengyang 421001, Peoples R China
[3] Sun Yat Sen Univ, Canc Ctr, State Key Lab Oncol South China, Guangzhou 510060, Peoples R China
[4] Univ South China, Affiliated Hosp 2, Hengyang Med Sch, Dept Urol Surg, Hengyang 421001, Peoples R China
关键词
Nasopharyngeal carcinoma; CKAP4; prognosis; metastasis; EMT; CKAP4;
D O I
10.1177/15353702231167940
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cytoskeleton-associated protein 4 (CKAP4) acts as a key transmembrane protein that connects the endoplasmic reticulum (ER) to microtubule dynamics. Researchers have not examined the roles of CKAP4 in nasopharyngeal carcinoma (NPC). The study aimed at evaluating the prognostic value and metastasis-regulating effect of CKAP4 in NPC. CKAP4 protein could be observed in 86.36% of 557 NPC specimens but not in normal nasopharyngeal epithelial tissue. According to immunoblot assays, NPC cell lines presented high CKAP4 expression relative to NP69 immortalized nasopharyngeal epithelial cells. Moreover, CKAP4 was highly expressed at the NPC tumor front and in matched liver, lung, and lymph node metastasis samples. Furthermore, high CKAP4 expression reported poor overall survival (OS) and presented a positive relevance to tumor (T) classification, recurrence, and metastasis. According to multivariate analysis, CKAP4 could independently and negatively predict patients' prognosis. Stable knockdown of CKAP4 expression in NPC cells inhibited cell migration, invasion and metastasis in vitro and in vivo. Moreover, CKAP4 promoted epithelial-mesenchymal transition (EMT) in NPC cells. CKAP4 knockdown was followed by the downregulation of the interstitial marker vimentin, and upregulation of the epithelial marker E-cadherin. In NPC tissues, high CKAP4 expression exhibited a positive relevance to vimentin expression and a negative relevance to E-cadherin expression. In conclusion, CKAP4 is an independent predictor of NPC, and CKAP4 might contribute NPC progression and metastasis, which may be involved in EMT with vimentin and E-cadherin.
引用
收藏
页码:1085 / 1094
页数:10
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