2011
DOI: 10.3342/ceo.2011.4.2.101
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The Role of Laryngopharyngeal Reflux as a Risk Factor in Laryngeal Cancer: A Preliminary Report

Abstract: ObjectivesTo evaluate the significance of laryngopharyngeal reflux (LPR) as a risk factor in laryngeal cancer.MethodsWe performed a case-control study with 29 consecutive laryngeal cancer patients who had undergone 24-hour ambulatory double pH monitoring from 2003 to 2006. The control group included 300 patients who had undergone 24-hour ambulatory double pH monitoring due to LPR-related symptoms. We analyzed the prevalence of LPR and numerous parameters from the 24-hour ambulatory double pH monitoring in the … Show more

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Cited by 47 publications
(58 citation statements)
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“…Use of coal (Sapkota et al, 2013) and silica dust exposure have also been implicated (Chen and Tsu, 2012). A similar irritation dependent mechanism might be relevant for the finding that gastrectomy for peptic ulcer disease might entail a long-term increase (Lagergren and Lindam, 2012) as does laryngopharyngeal reflux (Tae et al, 2011) but apparently not gastroesophageal reflux (Coca-Pelaz et al, 2013).…”
Section: Introductionmentioning
confidence: 99%
“…Use of coal (Sapkota et al, 2013) and silica dust exposure have also been implicated (Chen and Tsu, 2012). A similar irritation dependent mechanism might be relevant for the finding that gastrectomy for peptic ulcer disease might entail a long-term increase (Lagergren and Lindam, 2012) as does laryngopharyngeal reflux (Tae et al, 2011) but apparently not gastroesophageal reflux (Coca-Pelaz et al, 2013).…”
Section: Introductionmentioning
confidence: 99%
“…The medium was replaced with DMEM containing 20, 30 or 40 µM xanthohumol and cells were cultured for 48 h at 4˚C. SCC4 cells (1x10 6 ) were harvested, washed with PBS, and lysed with cold RIPA buffer (BestBio) containing protease inhibitors. Protein concentrations were quantified using the bicinchonic acid assay method (BestBio).…”
Section: Western Blot Analysis Scc4 Cells (24x10mentioning
confidence: 99%
“…The medium was replaced with DMEM containing 20, 30 or 40 µM xanthohumol and cells were cultured for 48 h at 4˚C. SCC4 cells (1x10 6 ) were harvested, washed with PBS and resuspended in binding buffer. A total of 1 µl fluorescent substrate [Ac-DEVD-pNA for caspase-3, Ac-IETD-pNA for caspase-8 and Ac-LEHD-pNA for caspase-9 (BestBio, Shanghai, China)] was added to each well and incubated for 1 h at 4˚C.…”
Section: Measurement Of Caspase-3 -8 and -9 Activity Scc4 Cells (2mentioning
confidence: 99%
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