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Clinicopathological and Prognostic Significance of SMAD4 in Non-small Cell Lung Cancer: A Meta-analysis and Database Validation

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Specialty General Medicine
Date 2023 Jul 21
PMID 37478236
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Abstract

Background: The relationship between SMAD family member 4 (SMAD4) and the clinicopathological and prognostic significance of non-small cell lung cancer (NSCLC) patients is unclear. Our aim was to investigate the association between SMAD4 expression and clinicopathological parameters and NSCLC prognosis.

Methods: We searched articles in databases from inception to July 2022 to retrieve literature related to SMAD4 expression and the clinicopathological and/or prognostic significance of NSCLC patients. Odds ratios (ORs), hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated. We evaluated the expression of SMAD4 and overall survival (OS) in NSCLC using the Kaplan-Meier plotter database.

Results: Eight articles with 1461 NSCLC patients were included. SMAD4 expression was related to tumor differentiation (OR = 0.359, 95% CI: 0.238-0.543, P = .000), lymph node metastasis (OR = 0.469, 95% CI: 0.04-0.725, P = .001), tumor node metastasis stage (OR = 0.238, 95% CI: 0.156-0.362, P = .000) and good OS (HR = 0.592, 95% CI: 0.332-0.853, P = .000) in NSCLC. There was no significant association between SMAD4 expression and age (OR = 0.822, 95% CI: 0.515-1.312, P = .411) or sex (OR = 1.056, 95% CI: 0.675-1.653, P = .811). Furthermore, SMAD4 expression was lower in NSCLC, and a good prognosis in NSCLC (HR = 0.6, 95% CI = 0.51-0.72, P = 4.2 e-9) was shown to correlate with higher SMAD4 expression using the Kaplan-Meier Plotter database.

Conclusion: SMAD4 expression is lower in NSCLC and correlated with lymph node metastasis, tumor differentiation, tumor node metastasis stage and good OS for NSCLC patients.

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References
1.
Liu J, Ren G, Li K, Liu Z, Wang Y, Chen T . The Smad4-MYO18A-PP1A complex regulates β-catenin phosphorylation and pemigatinib resistance by inhibiting PAK1 in cholangiocarcinoma. Cell Death Differ. 2021; 29(4):818-831. PMC: 8990017. DOI: 10.1038/s41418-021-00897-7. View

2.
Tong X, Liu H, Zhao H, Xu S, Li Y, Han L . [The role of Smad4 and MAPK proteins in signal transduction pathway in non-small cell lung cancer]. Zhonghua Zhong Liu Za Zhi. 2007; 28(10):741-5. View

3.
Javle M, Li Y, Tan D, Dong X, Chang P, Kar S . Biomarkers of TGF-β signaling pathway and prognosis of pancreatic cancer. PLoS One. 2014; 9(1):e85942. PMC: 3896410. DOI: 10.1371/journal.pone.0085942. View

4.
Ding Z, Wu C, Chu G, Xiao Y, Ho D, Zhang J . SMAD4-dependent barrier constrains prostate cancer growth and metastatic progression. Nature. 2011; 470(7333):269-73. PMC: 3753179. DOI: 10.1038/nature09677. View

5.
Wang Y, Xue Q, Zheng Q, Jin Y, Shen X, Yang M . SMAD4 mutation correlates with poor prognosis in non-small cell lung cancer. Lab Invest. 2020; 101(4):463-476. DOI: 10.1038/s41374-020-00517-x. View