TACC2 (transforming acidic coiled-coil protein 2) in breast carcinoma as a potent prognostic predictor associated with cell proliferation

被引:22
作者
Onodera, Yoshiaki [1 ]
Takagi, Kiyoshi [2 ]
Miki, Yasuhiro [1 ]
Takayama, Ken-ichi [3 ,4 ]
Shibahara, Yukiko [1 ]
Watanabe, Mika [5 ]
Ishida, Takanori [6 ]
Inoue, Satoshi [7 ,8 ]
Sasano, Hironobu [1 ,4 ]
Suzuki, Takashi [2 ]
机构
[1] Tohoku Univ, Grad Sch Med, Dept Anat Pathol, Sendai, Miyagi, Japan
[2] Tohoku Univ, Grad Sch Med, Pathol & Histotechnol, Sendai, Miyagi, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Antiaging Med, Tokyo, Japan
[4] Univ Tokyo, Grad Sch Med, Dept Geriatr Med, Tokyo, Japan
[5] Tohoku Univ Hosp, Dept Pathol, Sendai, Miyagi, Japan
[6] Tohoku Univ, Grad Sch Med, Surg Oncol, Sendai, Miyagi, Japan
[7] Saitama Med Univ, Res Ctr Genom Med, Div Gene Regulat & Signal Transduct, Hidaka, Saitama, Japan
[8] Tokyo Metropolitan Inst Gerontol, Funct Biogerontol, Tokyo, Japan
来源
CANCER MEDICINE | 2016年 / 5卷 / 08期
关键词
Breast cancer; prognostic markers; proliferation; TUMOR SUPPRESSOR; CANCER; ESTROGEN; ANDROGENS; GENES;
D O I
10.1002/cam4.736
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Transforming acidic coiled-coil protein 2 (TACC2) belongs to TACC family proteins and involved in a variety of cellular processes through interactions with some molecules involved in centrosomes/microtubules dynamics. Mounting evidence suggests that TACCs is implicated in the progression of some human malignancies, but significance of TACC2 protein in breast carcinoma is still unknown. Therefore, in this study, we examined the clinical significance of TACC2 in breast carcinoma and biological functions by immunohistochemistry and in vitro experiments. Immunohistochemistry for TACC2 was performed in 154 cases of invasive ductal carcinoma. MCF-7 and MDA-MB-453 breast carcinoma cell lines were transfected with small interfering RNA (siRNA) for TACC2, and subsequently, cell proliferation, 5-Bromo-2-deoxyuridine (BrdU), and invasion assays were performed. TACC2 immunoreactivity was detected in 78 out of 154 (51%) breast carcinoma tissues, and it was significantly associated with Ki-67 LI. The immunohistochemical TACC2 status was significantly associated with increased incidence of recurrence and breast cancer-specific death of the patients, and multivariate analyses demonstrated TACC2 status as an independent prognostic factor for both disease-free and breast cancer-specific survival. Subsequent in vitro experiments showed that TACC2 significantly increased the proliferation activity of MCF-7 and MDA-MB-453. These results suggest that TACC2 plays an important role in the cell proliferation of breast carcinoma and therefore immunohistochemical TACC2 status is a candidate of worse prognostic factor in breast cancer cases.
引用
收藏
页码:1973 / 1982
页数:10
相关论文
共 27 条
[1]   The tale of two domains - Proteomics and genomics analysis of SMYD2, a new histone methyltransferase [J].
Abu-Farha, Mohamed ;
Lambert, Jean-Philippe ;
Al-Madhoun, Ashraf S. ;
Elisma, Fred ;
Skerjanc, Ilona S. ;
Figeys, Daniel .
MOLECULAR & CELLULAR PROTEOMICS, 2008, 7 (03) :560-572
[2]   AZU-1:: A candidate breast tumor suppressor and biomarker for tumor progression [J].
Chen, HM ;
Schmeichel, KL ;
Mian, IS ;
Lelièvre, S ;
Petersen, OW ;
Bissell, MJ .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (04) :1357-1367
[3]  
Cheng Shan, 2010, Cancer Genomics & Proteomics, V7, P67
[4]   Genomic and transcriptional aberrations linked to breast cancer pathophysiologies [J].
Chin, Koei ;
DeVries, Sandy ;
Fridlyand, Jane ;
Spellman, Paul T. ;
Roydasgupta, Ritu ;
Kuo, Wen-Lin ;
Lapuk, Anna ;
Neve, Richard M. ;
Qian, Zuwei ;
Ryder, Tom ;
Chen, Fanqing ;
Feiler, Heidi ;
Tokuyasu, Taku ;
Kingsley, Chris ;
Dairkee, Shanaz ;
Meng, Zhenhang ;
Chew, Karen ;
Pinkel, Daniel ;
Jain, Ajay ;
Ljung, Britt Marie ;
Esserman, Laura ;
Albertson, Donna G. ;
Waldman, Frederic M. ;
Gray, Joe W. .
CANCER CELL, 2006, 10 (06) :529-541
[5]   Ki-67 as prognostic marker in early breast cancer: a meta-analysis of published studies involving 12 155 patients [J].
de Azambuja, E. ;
Cardoso, F. ;
de Castro, G., Jr. ;
Colozza, M. ;
Mano, M. S. ;
Durbecq, V. ;
Sotiriou, C. ;
Larsimont, D. ;
Piccart-Gebhart, M. J. ;
Paesmans, M. .
BRITISH JOURNAL OF CANCER, 2007, 96 (10) :1504-1513
[6]   An estrogen receptor-negative breast cancer subset characterized by a hormonally regulated transcriptional program and response to androgen [J].
Doane, A. S. ;
Danso, M. ;
Lal, P. ;
Donaton, M. ;
Zhang, L. ;
Hudis, C. ;
Gerald, W. L. .
ONCOGENE, 2006, 25 (28) :3994-4008
[7]   Identification of TACC1, NOV, and PTTG1 as new candidate genes associated with endocrine therapy resistance in breast cancer [J].
Ghayad, Sandra E. ;
Vendrell, Julie A. ;
Bieche, Ivan ;
Spyratos, Frederique ;
Dumontet, Charles ;
Treilleux, Isabelle ;
Lidereau, Rosette ;
Cohen, Pascale A. .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2009, 42 (1-2) :87-103
[8]   Transforming acidic coiled-coil proteins (TACCs) in human cancer [J].
Ha, Geun-Hyoung ;
Kim, Jung-Lye ;
Breuer, Eun-Kyoung Yim .
CANCER LETTERS, 2013, 336 (01) :24-33
[9]  
Hammond MEH, 2010, ARCH PATHOL LAB MED, V134, pE48, DOI 10.1043/1543-2165-134.7.e48
[10]   Systemic spread is an early step in breast cancer [J].
Huesemann, Yves ;
Geigl, Jochen B. ;
Schubert, Falk ;
Musiani, Piero ;
Meyer, Manfred ;
Burghart, Elke ;
Forni, Guido ;
Eils, Roland ;
Fehm, Tanja ;
Riethmueller, Gert ;
Klein, Christoph A. .
CANCER CELL, 2008, 13 (01) :58-68