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胰腺癌细胞系MIA PaCa-2中剪接变体MUC4/Y的上调增强增殖并抑制凋亡:对MUC4转录变体存在的新认识。

Upregulation of the splice variant MUC4/Y in the pancreatic cancer cell line MIA PaCa-2 potentiates proliferation and suppresses apoptosis: new insight into the presence of the transcript variant of MUC4.

作者信息

Xie Kunling, Zhi Xiaofei, Tang Jie, Zhu Yi, Zhang Jingjing, Li Zheng, Tao Jinqiu, Xu Zekuan

机构信息

Department of General Surgery, First Affiliated Hospital, Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.

出版信息

Oncol Rep. 2014 May;31(5):2187-94. doi: 10.3892/or.2014.3113. Epub 2014 Mar 27.

Abstract

MUC4/Y, the transcript variant 4 of MUC4, lacks exon 2 as compared with the transcript variant 1 of MUC4. To date, direct evidence for the function of MU4/Y remains to be reported. Previous studies based their hypotheses regarding the function of MUC4/Y on the characteristic structure domains of this variant. The aim of the present study was to investigate the specific function of MUC4/Y. The pancreatic cancer cell line MIA PaCa-2 with low MUC4/Y expression was used to establish a stable cell model of MUC4/Y upregulation using a lentivirus vector system. Results showed that MUC4/Y anchored on the cytomembrane and affected cell morphology and cell cycle. Functional analyses indicated that MUC4/Y upregulation slightly potentiated cell proliferation and significantly suppressed apoptosis both in vivo and in vitro. Further studies revealed that the JNK and AKT signalling pathways were activated. Meanwhile, MUC4/Y upregulation elicited minimal effect on the phosphorylation level of HER2, a membrane partner of MUC4. These results suggest that MUC4/Y promotes tumour progression through its anti-apoptotic and weak mitogenic effect on MIA PaCa-2 cells.

摘要

MUC4/Y是MUC4的转录变体4,与MUC4的转录变体1相比,缺少外显子2。迄今为止,关于MUC4/Y功能的直接证据仍有待报道。以往的研究基于该变体的特征性结构域对MUC4/Y的功能提出假设。本研究的目的是探究MUC4/Y的具体功能。使用低表达MUC4/Y的胰腺癌细胞系MIA PaCa-2,通过慢病毒载体系统建立MUC4/Y上调的稳定细胞模型。结果显示,MUC4/Y锚定在细胞膜上,并影响细胞形态和细胞周期。功能分析表明,MUC4/Y上调在体内和体外均轻微增强细胞增殖并显著抑制细胞凋亡。进一步研究发现JNK和AKT信号通路被激活。同时,MUC4/Y上调对MUC4的膜伴侣HER2的磷酸化水平影响极小。这些结果表明,MUC4/Y通过对MIA PaCa-2细胞的抗凋亡和微弱的促有丝分裂作用促进肿瘤进展。

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