» Articles » PMID: 26379819

Clinicopathological and Prognostic Significance of MUC4 Expression in Cancers: Evidence from Meta-analysis

Overview
Specialty General Medicine
Date 2015 Sep 18
PMID 26379819
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Mucin4 (MUC4) is a secreted glycoprotein. Numerous studies had indicated that MUC4 was an attractive prognostic tumor biomarker. However, the results of different studies have been inconsistent. So we conducted this meta-analysis to explore the association between MUC4 expression and cancer prognosis. A systematically comprehensive search was performed through PubMed, EMBASE and CNKI (Chinese National Knowledge Infrastructure). Prognostic value of MUC4 expression in malignancy patients was evaluated by pooled hazard ratios (HRs) and their 95% confidence intervals (CIs). Meanwhile, pooled odds ratio (OR) with 95% CI was appropriate for the association between MUC4 expression and clinicopathological parameters. Eighteen studies including 1,933 patients were enrolled in this meta-analysis. Significant association was found between elevated MUC4 expression and poorer overall survival (OS) with pooled hazard ratio (HR) of 1.87 [95% confidence interval (CI): 1.58-2.23, P<0.001]. Significant associations were also detected in biliary tract carcinoma (HR: 2.41, 95% CI: 1.69-3.42, P<0.001), pancreatic cancer (HR: 2.01, 95% CI: 1.42-2.86, P<0.001) and colorectal cancer (HR: 1.73, 95% CI: 1.17-2.54, P=0.006). Moreover, combined odds ratio (OR) of MUC4 indicated that MUC4 overexpression was associated with tumor stage, tumor invasion and lymph node metastasis. Our results demonstrated that MUC4 may be exploited as a novel prognostic biomarker for cancer patients.

Citing Articles

Molecular genetic analysis of colorectal carcinoma with an aggressive extraintestinal immunohistochemical phenotype.

Hrudka J, Kalinova M, Fiserova H, Jelinkova K, Nikov A, Waldauf P Sci Rep. 2024; 14(1):22241.

PMID: 39333321 PMC: 11437151. DOI: 10.1038/s41598-024-72687-3.


Potential Cause-and-Effect Relationship between Gut Microbiota and Childhood Neuroblastoma: A Mendelian Randomization Analysis.

Chu J Indian J Pediatr. 2024; .

PMID: 38536652 DOI: 10.1007/s12098-024-05065-6.


MUC13 negatively regulates tight junction proteins and intestinal epithelial barrier integrity via protein kinase C.

Segui-Perez C, Stapels D, Ma Z, Su J, Passchier E, Westendorp B J Cell Sci. 2024; 137(5).

PMID: 38345099 PMC: 10984281. DOI: 10.1242/jcs.261468.


Genetic variants of MUC4 are associated with susceptibility to and mortality of colorectal cancer and exhibit synergistic effects with LDL-C levels.

Kwon M, Lee J, Kim E, Ko E, Ryu C, Cho H PLoS One. 2023; 18(6):e0287768.

PMID: 37384668 PMC: 10310026. DOI: 10.1371/journal.pone.0287768.


Radiomics models based on multi-sequence MRI for preoperative evaluation of MUC4 status in pancreatic ductal adenocarcinoma: a preliminary study.

Deng Y, Li Y, Wu J, Zhou T, Tang M, Chen Y Quant Imaging Med Surg. 2022; 12(11):5129-5139.

PMID: 36330180 PMC: 9622441. DOI: 10.21037/qims-22-112.


References
1.
Higashi M, Yokoyama S, Yamamoto T, Goto Y, Kitazono I, Hiraki T . Mucin expression in endoscopic ultrasound-guided fine-needle aspiration specimens is a useful prognostic factor in pancreatic ductal adenocarcinoma. Pancreas. 2015; 44(5):728-34. PMC: 4464972. DOI: 10.1097/MPA.0000000000000362. View

2.
Jepson S, Komatsu M, Haq B, Arango M, Huang D, Carraway C . Muc4/sialomucin complex, the intramembrane ErbB2 ligand, induces specific phosphorylation of ErbB2 and enhances expression of p27(kip), but does not activate mitogen-activated kinase or protein kinaseB/Akt pathways. Oncogene. 2002; 21(49):7524-32. DOI: 10.1038/sj.onc.1205970. View

3.
Tierney J, Stewart L, Ghersi D, Burdett S, Sydes M . Practical methods for incorporating summary time-to-event data into meta-analysis. Trials. 2007; 8:16. PMC: 1920534. DOI: 10.1186/1745-6215-8-16. View

4.
Chauhan S, Singh A, Ruiz F, Johansson S, Jain M, Smith L . Aberrant expression of MUC4 in ovarian carcinoma: diagnostic significance alone and in combination with MUC1 and MUC16 (CA125). Mod Pathol. 2006; 19(10):1386-94. DOI: 10.1038/modpathol.3800646. View

5.
Polyak K, Kato J, Solomon M, Sherr C, Massague J, Roberts J . p27Kip1, a cyclin-Cdk inhibitor, links transforming growth factor-beta and contact inhibition to cell cycle arrest. Genes Dev. 1994; 8(1):9-22. DOI: 10.1101/gad.8.1.9. View