Overexpression of the pituitary tumor transforming gene upregulates metastasis in malignant neoplasms of the human salivary glands

被引:7
作者
Liu, Jia [1 ,2 ,3 ,4 ]
Wang, Yuguang [5 ]
He, Hong [2 ,3 ]
Jin, Wulong [1 ,4 ]
Zheng, Rong [4 ]
机构
[1] Wuhan Univ, State Key Lab Breeding Base Basic Sci Stomatol Hu, Wuhan 430079, Hubei, Peoples R China
[2] Wuhan Univ, Key Lab Oral Biomed Minist Educ, Wuhan 430079, Hubei, Peoples R China
[3] Wuhan Univ, Sch & Hosp Stomatol, Dept Orthodont, Wuhan 430079, Hubei, Peoples R China
[4] Inner Mongolia Med Univ, Affiliated Hosp, Dept Stomatol, Hohhot 010050, Inner Mongolia, Peoples R China
[5] Inner Mongolia Med Univ, Affiliated Hosp 2, Dept Diagnost Imaging, Hohhat 010030, Inner Mongolia, Peoples R China
基金
芬兰科学院;
关键词
pituitary tumor transforming gene; proliferation; metastasis; salivary glands malignant neoplasm; GROWTH-FACTOR RECEPTOR; MUCOEPIDERMOID CARCINOMA; EXPRESSION; CANCER; PTTG; PATHWAY;
D O I
10.3892/etm.2015.2566
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
Salivary gland malignant neoplasms (SGMNs) represent a group of malignant solid tumors with heterogeneity in their cellular make-up, which causes difficulty with regard to the immunohistochemical confirmation of their cytological features. In the present study, overexpression of the pituitary tumor transforming gene (PTTG) was evaluated in human mucoepidermoid carcinoma specimens with a submaxillary salivary gland origin by immunohistochemical analysis, western blot analysis and reverse transcription quantitative polymerase chain reaction. In addition, a SGMN cell line was constructed, namely A-253 PTTG (+), which overexpressed PTTG. Subsequently, the regulatory role of PTTG in the proliferation and migration of A-253 cells was investigated. The immunohistochemical results demonstrated that there was a higher rate of PTTG-positive cells in the SGMN tissues when compared with the control submaxillary salivary gland tissues. Furthermore, PTTG expression at a mRNA and protein level was significantly higher in the SGMN specimens when compared with the control specimens. In addition, the rates of proliferation and migration of the A-253 PTTG (+) cells were significantly higher compared with the A-253 PTTG (-) cells. Therefore, PTTG was demonstrated to play an important role in SGMN cell proliferation and migration, and may subsequently be a notable marker for SGMN diagnosis and a potential target for anticancer therapy.
引用
收藏
页码:763 / 768
页数:6
相关论文
共 24 条
[1]   Immunohistochemical expression of retinoblastoma pathway proteins in normal salivary glands and in salivary gland tumours [J].
Etges, A ;
Nunes, FD ;
Ribeiro, KCB ;
Araújo, VC .
ORAL ONCOLOGY, 2004, 40 (03) :326-331
[2]   Overexpression of EGFR and absence of C-KIT expression correlate with poor prognosis in salivary gland carcinomas [J].
Ettl, T. ;
Schwarz, S. ;
Kleinsasser, N. ;
Hartmann, A. ;
Reichert, T. E. ;
Driemel, O. .
HISTOPATHOLOGY, 2008, 53 (05) :567-577
[3]   Expression of pituitary-tumour transforming gene in colorectal tumours [J].
Heaney, AP ;
Singson, R ;
McCabe, CJ ;
Nelson, V ;
Nakashima, M ;
Melmed, S .
LANCET, 2000, 355 (9205) :716-719
[4]   Prognostic factors in major salivary gland cancer [J].
Hocwald, E ;
Korkmaz, H ;
Yoo, GH ;
Adsay, V ;
Shibuya, TY ;
Abrams, J ;
Jacobs, JR .
LARYNGOSCOPE, 2001, 111 (08) :1434-1439
[5]  
Honda S, 2003, ANTICANCER RES, V23, P3775
[6]   Securin is required for chromosomal stability in human cells [J].
Jallepalli, PV ;
Waizenegger, IC ;
Bunz, F ;
Langer, S ;
Speicher, MR ;
Peters, JM ;
Kinzler, KW ;
Vogelstein, B ;
Lengauer, C .
CELL, 2001, 105 (04) :445-457
[7]   Six1 Promotes Proliferation of Pancreatic Cancer Cells via Upregulation of Cyclin D1 Expression [J].
Li, Zhaoming ;
Tian, Tian ;
Lv, Feng ;
Chang, Yu ;
Wang, Xinhua ;
Zhang, Lei ;
Li, Xin ;
Li, Ling ;
Ma, Wang ;
Wu, Jingjing ;
Zhang, Mingzhi .
PLOS ONE, 2013, 8 (03)
[8]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408
[9]  
Lopes MA, 1998, HEAD NECK-J SCI SPEC, V20, P699, DOI 10.1002/(SICI)1097-0347(199812)20:8<699::AID-HED7>3.0.CO
[10]  
2-P