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. 2016 Jun 17:16:47.
doi: 10.1186/s12935-016-0325-2. eCollection 2016.

Prognostic value of CD44 expression in patients with hepatocellular carcinoma: meta-analysis

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Prognostic value of CD44 expression in patients with hepatocellular carcinoma: meta-analysis

Yangkun Luo et al. Cancer Cell Int. .

Abstract

Background: CD44 has been reported to be involved with tumor growth and metastasis and has also been implicated as a CSC marker in hepatocellular carcinoma (HCC). However, the prognostic value of CD44 still remains controversial; hence, we investigated the correlation between CD44 and the clinicopathological features of HCC by meta-analysis.

Methods: Identification and review of publications assessing clinical or prognostic significance of CD44 expression in HCC until November 1, 2015. A meta-analysis was performed to clarify the association between CD44 expression and clinical outcomes.

Results: A total of 14 publications met the criteria and comprised 2235 cases. Analysis of these data showed that CD44 expression was not significantly associated with the tumor differentiation (OR 1.48, 95 % confidence interval [CI] 0.85-2.60, P = 0.17), AFP level of HCC patients (OR 0.83, 95 % CI 0.52-1.33, P = 0.45), or disease-free survival (relative risk [RR] 1.15, 95 % CI, 0.85-1.54; P = 0.36). However, in the identified studies, CD44 expression was highly correlated with tumor TNM classification (OR 2.38, 95 % CI 1.23-4.60; P = 0.01) and decreased overall survival (RR 1.49, 95 % CI, 1.26-1.76; P < 0.00001).

Conclusions: This meta-analysis shows CD44 expression in HCC is connected with decreased overall and thus marks a worse prognosis.

Keywords: CD44; Disease-free survival; Meta-analysis; Overall survival; Prognosis.

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Figures

Fig. 1
Fig. 1
Literature search strategy and selection of articles
Fig. 2
Fig. 2
Forest plot depiction of CD44 expression and OR for clinical pathologic features. Clinicopathological parameters investigated are (a) TMN classification, (b) tumor grade (c)AFP level
Fig. 3
Fig. 3
Forest plot illustrates the association between CD44 expression and OS of HCC
Fig. 4
Fig. 4
Analysis of CD44 expression and DFS among included studies
Fig. 5
Fig. 5
Begg’s funnel plot estimated the publication bias of the included literature for OS (a) and DFS (b)
Fig. 6
Fig. 6
Sensitivity analysis of all the studies assessing OS (a) and DFS (b)

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References

    1. Ormandy LA, Hillemann T, Wedemeyer H, Manns MP, Greten TF, Korangy F. Increased populations of regulatory T cells in peripheral blood of patients with hepatocellular carcinoma. Cancer Res. 2005;65(6):2457–2464. doi: 10.1158/0008-5472.CAN-04-3232. - DOI - PubMed
    1. Lee J-S, Heo J, Libbrecht L, Chu IS, Kaposi-Novak P, Calvisi DF, Mikaelyan A, Roberts LR, Demetris AJ, Sun Z, Nevens F, Roskams T, Thorgeirsson SS. A novel prognostic subtype of human hepatocellular carcinoma derived from hepatic progenitor cells. Nat Med. 2006;12(4):410–416. doi: 10.1038/nm1377. - DOI - PubMed
    1. Malanchi I, Santamaria-Martínez A, Susanto E, Peng H, Lehr HA, Delaloye JF, Huelsken J. Interactions between cancer stem cells and their niche govern metastatic colonization. Nature. 2012;481(7379):85–89. doi: 10.1038/nature10694. - DOI - PubMed
    1. Eyler CE, Rich JN. Survival of the fittest: cancer stem cells in therapeutic resistance and angiogenesis. J Clin Oncol. 2008;26(17):2839–2845. doi: 10.1200/JCO.2007.15.1829. - DOI - PMC - PubMed
    1. Ma S. Biology and clinical implications of CD133 + liver cancer stem cells. Exp Cell Res. 2013;319(2):126–132. doi: 10.1016/j.yexcr.2012.09.007. - DOI - PubMed

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