AIM: To elucidate cell proliferation in erosive reflux disease (ERD) and non-erosive reflux disease (NERD), we evaluated markers in squamous epithelial cells. METHODS: Thirty-four consecutive patients with gastroesophageal-reflux-disease-related symptoms (21 NERD and 13 ERD) were evaluated for the enrolment into the study. All patients underwent 24-h pH monitoring, standard endoscopy, and biopsy for histological evaluation. The expression of cyclins D and A was evaluated by real-time reverse transcription polymerase chain reaction (RT-PCR) from isolated epithelial cells. In all samples, analysis of the isolated cell population revealed the presence of epithelial cells only. RESULTS: Real-time RT-PCR showed that, in patients with ERD, the relative expression of cyclin D1 mRNA in esophageal epithelium was strongly decreased in comparison with NERD patients. The mean value of relative expression of cyclin D1 mRNA in NERD patients was 3.44 ± 1.9, whereas in ERD patients, it was 1.32 ± 0.87 (P = 0.011). Real-time RT-PCR showed that, in patients with ERD, relative expression of cyclin A mRNA in esophageal epithelium was decreased in comparison with that in NERD patients (2.31 ± 2.87 vs 0.66 ± 1.11). The mean bromodeoxyurindine labeling index in the NERD patients was 5.42% ± 1.68%, whereas in ERD patients, it was 4.3% ± 1.59%. CONCLUSION: We confirmed reduced epithelial proliferation in ERD compared with NERD patients, and that individuals who develop ERD are characterized by weaker epithelial cell proliferation.

Cell proliferation of esophageal squamous epithelium in erosive and non-erosive reflux disease / C. Calabrese; L. Montanaro; G. Liguori; E. Brighenti; M. Vici; P. Gionchetti; F. Rizzello; M. Campieri; M. Derenzini; D. Trerè. - In: WORLD JOURNAL OF GASTROENTEROLOGY. - ISSN 1007-9327. - STAMPA. - 28:(2011), pp. 4496-4502. [10.3748/wjg.v17.i40.4496]

Cell proliferation of esophageal squamous epithelium in erosive and non-erosive reflux disease

CALABRESE, CARLO;MONTANARO, LORENZO;LIGUORI, GIUSEPPINA;BRIGHENTI, ELISA;VICI, MANUELA;GIONCHETTI, PAOLO;RIZZELLO, FERNANDO;CAMPIERI, MASSIMO;DERENZINI, MASSIMO;TRERE', DAVIDE
2011

Abstract

AIM: To elucidate cell proliferation in erosive reflux disease (ERD) and non-erosive reflux disease (NERD), we evaluated markers in squamous epithelial cells. METHODS: Thirty-four consecutive patients with gastroesophageal-reflux-disease-related symptoms (21 NERD and 13 ERD) were evaluated for the enrolment into the study. All patients underwent 24-h pH monitoring, standard endoscopy, and biopsy for histological evaluation. The expression of cyclins D and A was evaluated by real-time reverse transcription polymerase chain reaction (RT-PCR) from isolated epithelial cells. In all samples, analysis of the isolated cell population revealed the presence of epithelial cells only. RESULTS: Real-time RT-PCR showed that, in patients with ERD, the relative expression of cyclin D1 mRNA in esophageal epithelium was strongly decreased in comparison with NERD patients. The mean value of relative expression of cyclin D1 mRNA in NERD patients was 3.44 ± 1.9, whereas in ERD patients, it was 1.32 ± 0.87 (P = 0.011). Real-time RT-PCR showed that, in patients with ERD, relative expression of cyclin A mRNA in esophageal epithelium was decreased in comparison with that in NERD patients (2.31 ± 2.87 vs 0.66 ± 1.11). The mean bromodeoxyurindine labeling index in the NERD patients was 5.42% ± 1.68%, whereas in ERD patients, it was 4.3% ± 1.59%. CONCLUSION: We confirmed reduced epithelial proliferation in ERD compared with NERD patients, and that individuals who develop ERD are characterized by weaker epithelial cell proliferation.
2011
Cell proliferation of esophageal squamous epithelium in erosive and non-erosive reflux disease / C. Calabrese; L. Montanaro; G. Liguori; E. Brighenti; M. Vici; P. Gionchetti; F. Rizzello; M. Campieri; M. Derenzini; D. Trerè. - In: WORLD JOURNAL OF GASTROENTEROLOGY. - ISSN 1007-9327. - STAMPA. - 28:(2011), pp. 4496-4502. [10.3748/wjg.v17.i40.4496]
C. Calabrese; L. Montanaro; G. Liguori; E. Brighenti; M. Vici; P. Gionchetti; F. Rizzello; M. Campieri; M. Derenzini; D. Trerè
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/107037
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