» Articles » PMID: 27698811

Expression of FoxM1 and the EMT-associated Protein E-cadherin in Gastric Cancer and Its Clinical Significance

Overview
Journal Oncol Lett
Specialty Oncology
Date 2016 Oct 5
PMID 27698811
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

The aim of the present study was to investigate the expression of forkhead box M1 (FoxM1) and E-cadherin in tissues of gastric cancer in order to reveal any correlation between FoxM1, E-cadherin and clinicopathological parameters. The association between FoxM1 and E-cadherin in the development and progression of gastric cancer was also investigated. The expression of FoxM1 and E-cadherin in gastric cancer and adjacent normal tissue on tissue microarray was detected using immunohistochemistry. The clinicopathological significance of FoxM1 and E-cadherin in gastric cancer was explored, and the association between FoxM1 and E-cadherin was further examined using statistical techniques. In gastric cancer tissues, the expression of FoxM1 and E-cadherin was strongly positive, but it was weak in normal gastric mucosa. Overexpression of FoxM1 was evident in gastric cancer, and was associated with poor tumor differentiation (P<0.05), advanced tumor state (P<0.05) and lymph node (or distant) metastasis (P<0.05), whereas E-cadherin had the opposite effects. Furthermore, the correlation between FoxM1 and E-cadherin expression in gastric cancer tissue was negative. In conclusion, the high FoxM1 expression and low E-cadherin expression in gastric cancer tissue suggests that these proteins play a critical role in the development and progression of gastric cancer.

Citing Articles

Laminarin Attenuates ROS-Mediated Cell Migration and Invasiveness through Mitochondrial Dysfunction in Pancreatic Cancer Cells.

Lee W, Song G, Bae H Antioxidants (Basel). 2022; 11(9).

PMID: 36139787 PMC: 9495390. DOI: 10.3390/antiox11091714.


A narrative review of research progress on FoxM1 in breast cancer carcinogenesis and therapeutics.

Zhang Y, Ma Y, Zeng Y, Liu Y, He E, Liu Y Ann Transl Med. 2022; 9(22):1704.

PMID: 34988213 PMC: 8667115. DOI: 10.21037/atm-21-5271.


Downregulation of lncRNA inhibits proliferation and migration of mesothelioma cells by targeting .

Fujii Y, Amatya V, Kushitani K, Suzuki R, Kai Y, Kambara T Oncol Rep. 2021; 47(2).

PMID: 34859258 PMC: 8674703. DOI: 10.3892/or.2021.8238.


Epithelial expression of epithelia-cadherin in different grades of oral squamous cell carcinoma.

Kar D, Banerjee S J Oral Maxillofac Pathol. 2021; 25(2):253-257.

PMID: 34703118 PMC: 8491325. DOI: 10.4103/0973-029X.325123.


Circular PVT1 regulates cell proliferation and invasion via miR-149-5p/FOXM1 axis in ovarian cancer.

Li M, Chi C, Zhou L, Chen Y, Tang X J Cancer. 2021; 12(2):611-621.

PMID: 33391456 PMC: 7738991. DOI: 10.7150/jca.52234.


References
1.
Yatsuya H, Toyoshima H, Mizoue T, Kondo T, Tamakoshi K, Hori Y . Family history and the risk of stomach cancer death in Japan: differences by age and gender. Int J Cancer. 2002; 97(5):688-94. DOI: 10.1002/ijc.10101. View

2.
Kong F, Zhu Y, Yuan H, Wang J, Zhao M, Gong X . FOXM1 regulated by ERK pathway mediates TGF-β1-induced EMT in NSCLC. Oncol Res. 2015; 22(1):29-37. PMC: 7592790. DOI: 10.3727/096504014X14078436004987. View

3.
Halasi M, Gartel A . Targeting FOXM1 in cancer. Biochem Pharmacol. 2012; 85(5):644-652. DOI: 10.1016/j.bcp.2012.10.013. View

4.
Tang W, Zhu Y, Gao J, Fu J, Liu C, Liu Y . MicroRNA-29a promotes colorectal cancer metastasis by regulating matrix metalloproteinase 2 and E-cadherin via KLF4. Br J Cancer. 2013; 110(2):450-8. PMC: 3899762. DOI: 10.1038/bjc.2013.724. View

5.
Wang Y, Yao B, Wang Y, Zhang M, Fu S, Gao H . Increased FoxM1 expression is a target for metformin in the suppression of EMT in prostate cancer. Int J Mol Med. 2014; 33(6):1514-22. DOI: 10.3892/ijmm.2014.1707. View