TACC3 promotes colorectal cancer tumourigenesis and correlates with poor prognosis.
TACC3 promotes colorectal cancer tumourigenesis and correlates with poor prognosis.
复制标题
TACC3 促进结直肠癌肿瘤发生并与不良预后相关
DOI:
10.18632/oncotarget.9628
复制
发表时间:
2016-07-05
期刊:
影响因子:
--
通讯作者:
Liu H
中科院分区:
文献类型:
--
作者:
Du Y;Liu L;Wang C;Kuang B;Yan S;Zhou A;Wen C;Chen J;Wu Y;Yang X;Feng G;Liu B;Iwamoto A;Zeng M;Wang J;Zhang X;Liu H
Colorectal carcinoma (CRC) is a malignant epithelial tumour with tremendous invasion and metastatic capacity. Transforming acidic coiled-coil protein-3 (TACC3), a frequently aberrantly expressed oncogene, is an important biomarker in various human cancers. Our study aimed to investigate the expression and function of TACC3 in human CRC. We found that TACC3 was over-expressed at both the mRNA and protein levels in CRC cells and in biopsies of CRC tissues compared with normal controls as determined by qRT-PCR, western blot and immunohistochemical (IHC) staining assays. IHC staining of samples from 161 patients with CRC also revealed that TACC3 expression was significantly correlated with clinical stage (P = 0.045), T classification (P = 0.029) and M classification (P = 0.020). Multivariate analysis indicated that high TACC3 expression was an independent prognostic marker for CRC. Patients who had high TACC3 expression had significantly poorer overall survival (OS, P = 0.023) and disease-free survival (DFS, P = 0.019) compared to patients who had low TACC3 expression. Furthermore, TACC3 knockdown attenuated CRC cell proliferation, colony formation capability, migration and invasion capability, and tumourigenesis in nude mice; these properties were measured using a real-time cell analyser (RTCA), clonogenicity analysis, and transwell and xenograft assays, respectively. These data indicate that TACC3 promotes CRC progression and could be an independent prognostic factor and a potential therapeutic target for CRC.
登录
查看更多内容
影响因子:
--
作者:
Duncan CG;Killela PJ;Payne CA;Lampson B;Chen WC;Liu J;Solomon D;Waldman T;Towers AJ;Gregory SG;McDonald KL;McLendon RE;Bigner DD;Yan H
通讯作者:
Yan H
DOI:
10.1073/pnas.1513359112
发表时间:
2015-09-01
影响因子:
11.1
作者:
Xiong, Dan;Du, Yong;Zeng, Mu-Sheng
通讯作者:
Zeng, Mu-Sheng
影响因子:
3.7
作者:
Mahdipour M;Leitoguinho AR;Zacarias Silva RA;van Tol HT;Stout TA;Rodrigues G;Roelen BA
通讯作者:
Roelen BA
影响因子:
--
作者:
Huang ZL;Lin ZR;Xiao YR;Cao X;Zhu LC;Zeng MS;Zhong Q;Wen ZS
通讯作者:
Wen ZS
影响因子:
11.2
作者:
LeRoy, Patrick J.;Hunter, John J.;Ecsedy, Jeffrey A.
通讯作者:
Ecsedy, Jeffrey A.