Increased tensin 4 expression is related to the histological type of gastric cancer

被引:3
作者
Niziol, Marcin [1 ]
Zinczuk, Justyna [2 ]
Zareba, Konrad [3 ]
Guzinska-Ustymowicz, Katarzyna [1 ]
Pryczynicz, Anna [1 ]
机构
[1] Med Univ Bialystok, Dept Gen Pathomorphol, Kilinskiego 1, PL-15089 Bialystok, Poland
[2] Med Univ Bialystok, Dept Clin Lab Diagnost, PL-15089 Bialystok, Poland
[3] Med Univ Bialystok, Clin Dept Gen & Gastroenterol Surg 2, PL-15089 Bialystok, Poland
来源
WORLD JOURNAL OF CLINICAL ONCOLOGY | 2021年 / 12卷 / 12期
关键词
Gastric cancer; Tensin; 4; Adhesion proteins; Immunohistochemistry; MESSENGER-RNA EXPRESSION; TUMOR PROGRESSION; CELL MOTILITY; CTEN; CLASSIFICATION; CARCINOMA; PROGNOSIS; PROMOTES; ONCOGENE; KINASE;
D O I
10.5306/wjco.v12.i12.1202
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUNDGastric cancer (GC) is one of the most common malignant tumors worldwide. Tensin 4 (TNS4) is an adhesive protein belonging to the tensin family. This protein is located in focal adhesion sites. The TNS4 gene is considered an oncogene in numerous cancers. This protein plays an important role in adhesion, migration and proliferation of cells.AIMTo evaluate expression of TNS4 protein in GC tissues and analysis of the clinical and histopathological parameters as well as the overall survival rate of patients.METHODSThe expression of TNS4 was assessed in 89 patients using immunohistochemistry.RESULTSPositive expression of TNS4 was observed in 49 of 89 patients (55.06%). Higher TNS4 expression was more common in GC tumors with a diameter & GE; 5 cm (P = 0.040). We demonstrated that an increase in TNS4 expression was more frequent in tumors of the histological type without mucinous components than in tumors from mucosal cancers (P = 0.023). Furthermore, TNS4 expression was higher in moderately differentiated tumors than in poorly differentiated and non-differentiated tumors (P = 0.002). Increased TNS4 expression was also noted in the intestinal type of GC according to Lauren's classification (P = 0.020). No statistically significant correlation was found between the expression of TNS4 and the overall survival rate of patients.CONCLUSIONTNS4 expression was significantly higher in tumors with a diameter & GE; 5 cm of the moderately differentiated intestinal type (according to Lauren's classification) of GC without a mucinous component. Therefore, increased TNS4 expression is related to the histological type of GC with a better prognosis.
引用
收藏
页码:1202 / 1214
页数:13
相关论文
共 37 条
[1]  
Adachi Y, 2000, CANCER-AM CANCER SOC, V89, P1418
[2]   C-Terminal Tensin-Like Gene Functions as an Oncogene and Promotes Cell Motility in Pancreatic Cancer [J].
Al-Ghamdi, Saleh ;
Cachat, Julien ;
Albasri, Abdulkader ;
Ahmed, Mohammed ;
Jackson, Darryl ;
Zaitoun, Abed ;
Guppy, Naomi ;
Otto, William R. ;
Alison, Malcolm R. ;
Kindle, Karin B. ;
Ilyas, Mohammad .
PANCREAS, 2013, 42 (01) :135-140
[3]   Cten signals through integrin-linked kinase (ILK) and may promote metastasis in colorectal cancer [J].
Albasri, A. ;
Al-Ghamdi, S. ;
Fadhil, W. ;
Aleskandarany, M. ;
Liao, Y-C ;
Jackson, D. ;
Lobo, D. N. ;
Lo, S. H. ;
Kumari, R. ;
Durrant, L. ;
Watson, S. ;
Kindle, K. B. ;
Ilyas, M. .
ONCOGENE, 2011, 30 (26) :2997-3002
[4]  
Albasri A, 2014, ANTICANCER RES, V34, P3969
[5]   CTEN (C-terminal tensin-like), a novel oncogene overexpressed in invasive breast carcinoma of poor prognosis [J].
Albasri, Abdulkader ;
Aleskandarany, Mohammed ;
Benhasouna, Ahmed ;
Powe, Desmond G. ;
Ellis, Ian O. ;
Ilyas, Mohammad ;
Green, Andrew R. .
BREAST CANCER RESEARCH AND TREATMENT, 2011, 126 (01) :47-54
[6]   C-terminal Tensin-like (CTEN) is an oncogene which alters cell motility possibly through repression of E-cadherin in colorectal cancer [J].
Albasri, Abdulkader ;
Seth, Rashmi ;
Jackson, Darryl ;
Benhasouna, Ahmed ;
Crook, Simon ;
Nateri, Abdolrahman S. ;
Chapman, Roger ;
Ilyas, Mohammad .
JOURNAL OF PATHOLOGY, 2009, 218 (01) :57-65
[7]  
Aratani Kenichi, 2019, Oncotarget, V10, P5726, DOI 10.18632/oncotarget.27229
[8]   Cten promotes Epithelial-Mesenchymal Transition (EMT) in colorectal cancer through stabilisation of Src [J].
Asiri, Abdulaziz ;
Toss, Michael S. ;
Raposo, Teresa Pereira ;
Akhlaq, Maham ;
Thorpe, Hannah ;
Alfahed, Abdulaziz ;
Asiri, Abutaleb ;
Ilyas, Mohammad .
PATHOLOGY INTERNATIONAL, 2019, 69 (07) :381-391
[9]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[10]  
Chan LK, 2015, ONCOTARGET, V6