2012
DOI: 10.1016/j.oraloncology.2012.06.010
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Prognostic value of the chemokine receptor CXCR4 and epithelial-to-mesenchymal transition in patients with squamous cell carcinoma of the mobile tongue

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Cited by 31 publications
(35 citation statements)
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“…Immunohistochemistry studies have found that CXCR4 expression levels are significantly higher in the tumors of patients with regional involvement at the initial evaluation (N?) [10,11,[15][16][17][18]. Considering the transcriptional expression, Ueda et al [12] found a significant relationship in HNSCC patients between CXCR4 mRNA values measured by RT-PCR and the regional status.…”
Section: Discussionmentioning
confidence: 99%
“…Immunohistochemistry studies have found that CXCR4 expression levels are significantly higher in the tumors of patients with regional involvement at the initial evaluation (N?) [10,11,[15][16][17][18]. Considering the transcriptional expression, Ueda et al [12] found a significant relationship in HNSCC patients between CXCR4 mRNA values measured by RT-PCR and the regional status.…”
Section: Discussionmentioning
confidence: 99%
“…An elimination of epithelial markers, including E-cadherin and β-catenin, and an increase in mesenchymal markers, including vimentin, SNAIL, and NG-cadherin, facilitate the degradation of the extracellular matrix, which relies on matrix metalloproteinases (MMPs) [75] . The CXCL12/CXCR4 axis was significantly correlated with EMT-associated proteins in OSCC [46] . Ou et al [76] suggested that the EMT-related transcription factor TWIST regulates CXCR4 expression and that TWIST overexpression was associated with lymph node metastasis.…”
Section: Clinical Implications Of Cxcr4 Pathway In Hnsccmentioning
confidence: 93%
“…HNSCC patients with high levels of CXCR4 protein and/or RNA expression demonstrated a higher rate of lymph node and distant metastases, and loco-regional recurrence, and a significantly reduced chance of being metastasis free and the likelihood of overall survival. Interestingly, the clinical outcome in patients with high levels of CXCL12 expression, the reverse was observed [46,51,66,[81][82][83][84][85] . Since CXCL12/CXCR4 was demonstrated to be involved in more than 20 different human cancers, it has been thought that CXCR4 antagonism could reduce tumour cell growth, migration, and chemotaxis [86] .…”
Section: Clinical Implications Of Cxcr4 Pathway In Hnsccmentioning
confidence: 96%
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“…Meng et al, 2010;Albert et al, 2012 CD166 (ALCAM) -Recently recognized as a potential membrane associated stem cell marker. -In HNSCC, over expression of CD166+ cells demonstrate a greater sphere formation ability in vitro, tumour formation ability in vivo and are positively correlated with poor patient outcome & higher tumour recurrence rates.…”
Section: Sabine Et Al 2008)mentioning
confidence: 99%