The In Vitro Effect of Acidic-Pepsin on Nuclear Factor KappaB Activation and Its Related Oncogenic Effect on Normal Human Hypopharyngeal Cells.

ABSTRACT:

Background

Extra-esophageal carcinogenesis has been widely discussed in relation to the chronic effects of laryngopharyngeal reflux and most prominently with pepsin historically central to this discussion. With refluxate known to include gastric (pepsin) and duodenal (bile) fluids, we recently demonstrated the mechanistic role of NF-?B in mediating the preneoplastic effects of acidic-bile. However, the role of pepsin in promoting hypopharyngeal premalignant events remains historically unclear. Here, we investigate the in vitro effect of acidic-pepsin on the NF-?B oncogenic pathway to better define its potential role in hypopharyngeal neoplasia.

Methods

Human hypopharyngeal primary cells (HHPC) and keratinocytes (HHK) were repetitively exposed to physiologic pepsin concentrations (0.1 mg/ml) at pH 4.0, 5.0 and 7.0. Cellular localization of phospho-NF-?B and bcl-2 was determined using immunofluorescence and western blotting. NF-?B transcriptional activity was tested by luc reporter and qPCR. Analysis of DNA content of pepsin treated HHK and HHPC was performed using Fluorescence-activated-cell sorting assay. To explore a possible dose related effect, pepsin concentration was reduced from 0.1 to 0.05 and 0.01 mg/ml.

Results

At physiologic concentration, acidic-pepsin (0.1 mg/ml at pH 4.0) is lethal to most normal hypopharyngeal cells. However, in surviving cells, no NF-?B transcriptional activity is noted. Acidic-pepsin fails to activate the NF-?B or bcl-2, TNF-?, EGFR, STAT3, and wnt5? but increases the Tp53 mRNAs, in both HHPC and HHK. Weakly acidic-pepsin (pH 5.0) and neutral-pepsin (pH 7.0) induce mild activation of NF-?B with increase in TNF-? mRNAs, without oncogenic transcriptional activity. Lower concentrations of pepsin at varying pH do not produce NF-?B activity or transcriptional activation of the analyzed genes.

Conclusion

Our findings in vitro do not support the role of acidic-pepsin in NF-?B related hypopharyngeal carcinogenesis.

SUBMITTER: Sasaki CT 

PROVIDER: S-EPMC5156414 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature