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2
Annexin A1-suppressed autophagy promotes nasopharyngeal carcinoma cell invasion and metastasis by PI3K/AKT signaling activation.膜联蛋白 A1 抑制自噬通过 PI3K/AKT 信号通路激活促进鼻咽癌细胞侵袭和转移。
Cell Death Dis. 2018 Nov 20;9(12):1154. doi: 10.1038/s41419-018-1204-7.
3
Microtubule Acetylation Is Required for Mechanosensation in Drosophila.微管乙酰化对于果蝇的机械感觉至关重要。
Cell Rep. 2018 Oct 23;25(4):1051-1065.e6. doi: 10.1016/j.celrep.2018.09.075.
4
Overexpression of KIF2A is Suppressed by miR-206 and Associated with Poor Prognosis in Ovarian Cancer.KIF2A的过表达被miR-206抑制,并与卵巢癌的不良预后相关。
Cell Physiol Biochem. 2018;50(3):810-822. doi: 10.1159/000494467. Epub 2018 Oct 23.
5
Mitosis-specific MRN complex promotes a mitotic signaling cascade to regulate spindle dynamics and chromosome segregation.有丝分裂特异性 MRN 复合物促进有丝分裂信号级联反应,以调节纺锤体动力学和染色体分离。
Proc Natl Acad Sci U S A. 2018 Oct 23;115(43):E10079-E10088. doi: 10.1073/pnas.1806665115. Epub 2018 Oct 8.
6
External validity of a prognostic nomogram for locoregionally advanced nasopharyngeal carcinoma based on the 8th edition of the AJCC/UICC staging system: a retrospective cohort study.基于第 8 版 AJCC/UICC 分期系统的局部晚期鼻咽癌预后列线图的外部有效性:一项回顾性队列研究。
Cancer Commun (Lond). 2018 Sep 3;38(1):55. doi: 10.1186/s40880-018-0324-x.
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Therapy-induced stress response is associated with downregulation of pre-mRNA splicing in cancer cells.治疗诱导的应激反应与癌细胞中前体 mRNA 剪接的下调有关。
Genome Med. 2018 Jun 27;10(1):49. doi: 10.1186/s13073-018-0557-y.
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Down-regulation of KIF2A inhibits gastric cancer cell invasion via suppressing MT1-MMP.KIF2A的下调通过抑制MT1-MMP来抑制胃癌细胞的侵袭。
Clin Exp Pharmacol Physiol. 2018 Oct;45(10):1010-1018. doi: 10.1111/1440-1681.12974. Epub 2018 Jun 26.
9
Development and validation of a gene expression-based signature to predict distant metastasis in locoregionally advanced nasopharyngeal carcinoma: a retrospective, multicentre, cohort study.基于基因表达signature 预测局部晚期鼻咽癌远处转移的建立和验证:一项回顾性、多中心队列研究。
Lancet Oncol. 2018 Mar;19(3):382-393. doi: 10.1016/S1470-2045(18)30080-9. Epub 2018 Feb 7.
10
Overexpression of Nogo receptor 3 (NgR3) correlates with poor prognosis and contributes to the migration of epithelial cells of nasopharyngeal carcinoma patients.Nogo 受体 3(NgR3)的过表达与预后不良相关,并促进鼻咽癌患者上皮细胞的迁移。
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KIF2A对鼻咽癌及鼻咽癌细胞预后的影响。

Effects of KIF2A on the prognosis of nasopharyngeal carcinoma and nasopharyngeal carcinoma cells.

作者信息

Zhang Qiuchan, Lu Dongling, Liu Wenlin, Ye Shijie, Guo Huanping, Liao Tianyi, Chen Cuifang

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan People's Hospital, Qingyuan, Guangdong 511518, P.R. China.

出版信息

Oncol Lett. 2019 Sep;18(3):2718-2723. doi: 10.3892/ol.2019.10597. Epub 2019 Jul 9.

DOI:10.3892/ol.2019.10597
PMID:31452750
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6676658/
Abstract

Nasopharyngeal carcinoma (NPC) is a common tumor in south China. Kinesin family member 2A (KIF2A) belongs to the kinesin-13 family and is associated with the growth and invasion of a number of different types of human cancer, including ovarian, breast and prostate cancer. The aim of the present study was to evaluate the expression of KIF2A in NPC and explore the relationship between KIF2A and the basic characteristics of 5-8F cells. Immunohistochemistry was performed on tissues from 97 patients with NPC to assess KIF2A protein expression. KIF2A was knocked down by a specific short interfering (si)RNA in 5-8F cell lines. Cell proliferation, apoptosis and cycle were analyzed by MTT assay and flow cytometry. The invasive ability and angiogenesis were evaluated by Matrigel assay and reverse transcription-quantitative PCR. The level of KIF2A was associated with the growth and migration of primary tumor, nodal status and tumor stage. The viability of KIF2A-knockdown cells was decreased compared with that of the control cells. The number of apoptotic cells, as well as the percentage of cells in the G0/G1 phase, was higher in the KIF2A siRNA group compared with the control group. The invasive and angiogenetic ability of 5-8F cells in the KIF2A siRNA group was decreased compared with the control group. In conclusion, the expression of KIF2A correlated with the poor clinicopathological features in NPC. Therefore, KIF2A may serve an important role in the progression of NPC and proliferation of 5-8F cells, which might present a potential therapeutic target for patients with NPC.

摘要

鼻咽癌(NPC)是中国南方常见的肿瘤。驱动蛋白家族成员2A(KIF2A)属于驱动蛋白-13家族,与多种不同类型的人类癌症的生长和侵袭相关,包括卵巢癌、乳腺癌和前列腺癌。本研究的目的是评估KIF2A在鼻咽癌中的表达,并探讨KIF2A与5-8F细胞基本特征之间的关系。对97例鼻咽癌患者的组织进行免疫组织化学检测,以评估KIF2A蛋白表达。在5-8F细胞系中用特异性短发夹干扰(si)RNA敲低KIF2A。通过MTT法和流式细胞术分析细胞增殖、凋亡和周期。通过基质胶试验和逆转录-定量PCR评估侵袭能力和血管生成。KIF2A水平与原发肿瘤的生长和迁移、淋巴结状态及肿瘤分期相关。与对照细胞相比,KIF2A敲低细胞的活力降低。与对照组相比,KIF2A siRNA组的凋亡细胞数量以及G0/G1期细胞百分比更高。与对照组相比,KIF2A siRNA组5-8F细胞的侵袭和血管生成能力降低。总之,KIF2A的表达与鼻咽癌不良的临床病理特征相关。因此,KIF2A可能在鼻咽癌进展和5-8F细胞增殖中起重要作用,这可能为鼻咽癌患者提供一个潜在的治疗靶点。