» Articles » PMID: 25674238

Up-regulation of ECT2 is Associated with Poor Prognosis in Gastric Cancer Patients

Overview
Specialty Pathology
Date 2015 Feb 13
PMID 25674238
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: The aim of this study was to investigate the expression of ECT2 in gastric cancer and its clinical significance.

Methods And Results: We investigated the differentially expressed genes between gastric cancer tissues and normal gastric mucosa by cDNA microarray, and then we found ECT2 was up-regulated in gastric cancer. What is more, we verified ECT2 expression level by quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR) and measured its protein level by immunohistochemistry (IHC). qRT-PCR analysis indicated ECT2 was significantly up-regulated in gastric cancer and Immunohistochemistry confirmed the percentage of ECT2-positive specimens was significantly higher in gastric carcinoma than in non-tumor tissues. Up-regulation of ECT2 is associated with the degree of histological differentiation (P = 0.007), invasion depth (P = 0.047), lymph node metastasis (P = 0.016), distant metastasis (P = 0.021) and TNM stage (P = 0.016), patients with up-regulated ECT2 had a lower overall survival rate (P = 0.000). Cox regression analysis revealed that up-regulation of ECT2 is an independent prognostic factor in gastric cancer patients (P = 0.012).

Conclusion: Up-regulation of ECT2 might contribute to the progression of gastric carcinogenesis and may be a useful prognostic indicator in gastric cancer.

Citing Articles

RHOA drives the development of diffuse gastric cancer through IGF1R-PAK1-YAP1 signaling.

Schaefer A, Hodge R, Zhang H, Hobbs G, Dilly J, Huynh M Sci Signal. 2023; 16(816):eadg5289.

PMID: 38113333 PMC: 10791543. DOI: 10.1126/scisignal.adg5289.


A Comprehensive Pan-Cancer Analysis Identifies CEP55 as a Potential Oncogene and Novel Therapeutic Target.

Zaki M, Eldeen M, K Abdulsahib W, Shati A, Alqahtani Y, Al-Qahtani S Diagnostics (Basel). 2023; 13(9).

PMID: 37175004 PMC: 10178510. DOI: 10.3390/diagnostics13091613.


Integration of Chemoinformatics and Multi-Omics Analysis Defines ECT2 as a Potential Target for Cancer Drug Therapy.

Soltan M, Eldeen M, Sajer B, Abdelhameed R, Al-Salmi F, Fayad E Biology (Basel). 2023; 12(4).

PMID: 37106813 PMC: 10135641. DOI: 10.3390/biology12040613.


Identification of key genes and carcinogenic pathways in hepatitis B virus-associated hepatocellular carcinoma through bioinformatics analysis.

Kim S, Hwang S, Song G, Jung D, Moon D, Yang J Ann Hepatobiliary Pancreat Surg. 2021; 26(1):58-68.

PMID: 34907098 PMC: 8901975. DOI: 10.14701/ahbps.21-108.


Aberrant Expression and Subcellular Localization of ECT2 Drives Colorectal Cancer Progression and Growth.

Cook D, Kang M, Martin T, Galanko J, Loeza G, Trembath D Cancer Res. 2021; 82(1):90-104.

PMID: 34737214 PMC: 9056178. DOI: 10.1158/0008-5472.CAN-20-4218.


References
1.
Gravalos C, Jimeno A . HER2 in gastric cancer: a new prognostic factor and a novel therapeutic target. Ann Oncol. 2008; 19(9):1523-9. DOI: 10.1093/annonc/mdn169. View

2.
Yang L . Incidence and mortality of gastric cancer in China. World J Gastroenterol. 2006; 12(1):17-20. PMC: 4077485. DOI: 10.3748/wjg.v12.i1.17. View

3.
Tamura G . Alterations of tumor suppressor and tumor-related genes in the development and progression of gastric cancer. World J Gastroenterol. 2006; 12(2):192-8. PMC: 4066026. DOI: 10.3748/wjg.v12.i2.192. View

4.
Gomez del Pulgar T, Benitah S, Valeron P, Espina C, Lacal J . Rho GTPase expression in tumourigenesis: evidence for a significant link. Bioessays. 2005; 27(6):602-13. DOI: 10.1002/bies.20238. View

5.
Solski P, Wilder R, Rossman K, Sondek J, Cox A, Campbell S . Requirement for C-terminal sequences in regulation of Ect2 guanine nucleotide exchange specificity and transformation. J Biol Chem. 2004; 279(24):25226-33. DOI: 10.1074/jbc.M313792200. View