Gastric Carcinogenesis and Potential Role of the Transient Receptor Potential Vanilloid 1 (TRPV1) Receptor: An Observational Histopathological Study

被引:0
作者
Groen, Sylvester R. [1 ]
Keszthelyi, Daniel [1 ]
Szallasi, Arpad [2 ]
van Veghel, Jara A. [1 ]
Alleleyn, Annick M. E. [1 ]
Cseko, Kata [3 ,4 ,5 ]
Helyes, Zsuzsanna [3 ,4 ,5 ]
Samarska, Iryna [6 ]
Grabsch, Heike I. [6 ,7 ]
Masclee, Ad A. M. [1 ]
Weerts, Zsa Zsa R. M. [1 ]
机构
[1] Maastricht Univ Med Ctr, NUTRIM Sch Nutr & Translat Res Metab, Dept Gastroenterol & Hepatol, NL-6629 HX Maastricht, Netherlands
[2] Semmelweis Univ, Dept Pathol & Expt Canc Res, H-1083 Budapest, Hungary
[3] Univ Pecs, Med Sch, Dept Pharmacol & Pharmacotherapy, H-7624 Pecs, Hungary
[4] Univ Pecs, HUN REN Chron Pain Res Grp, H-7624 Pecs, Hungary
[5] Natl Lab Drug Res & Dev, H-1117 Budapest, Hungary
[6] Maastricht Univ Med Ctr, Dept Pathol, NL-6629 HX Maastricht, Netherlands
[7] Univ Leeds, Leeds Inst Med Res St Jamess Univ, Div Pathol & Data Analyt, Leeds LS2 9JT, England
关键词
TRPV1; transient receptor potential vanilloid-1; gastritis; H; pylori; gastric cancer; intestinal metaplasia; CAPSAICIN; CANCER; CHANNELS; EXPRESSION; DIAGNOSIS; GENOTYPES;
D O I
10.3390/ijms25158294
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The potential role of the transient receptor potential Vanilloid 1 (TRPV1) non-selective cation channel in gastric carcinogenesis remains unclear. The main objective of this study was to evaluate TRPV1 expression in gastric cancer (GC) and precursor lesions compared with controls. Patient inclusion was based on a retrospective review of pathology records. Patients were subdivided into five groups: Helicobacter pylori (H. pylori)-associated gastritis with gastric intestinal metaplasia (GIM) (n = 12), chronic atrophic gastritis (CAG) with GIM (n = 13), H. pylori-associated gastritis without GIM (n = 19), GC (n = 6) and controls (n = 5). TRPV1 expression was determined with immunohistochemistry and was significantly higher in patients with H. pylori-associated gastritis compared with controls (p = 0.002). TRPV1 expression was even higher in the presence of GIM compared with patients without GIM and controls (p < 0.001). There was a complete loss of TRPV1 expression in patients with GC. TRPV1 expression seems to contribute to gastric-mucosal inflammation and precursors of GC, which significantly increases in cancer precursor lesions but is completely lost in GC. These findings suggest TRPV1 expression to be a potential marker for precancerous conditions and a target for individualized treatment. Longitudinal studies are necessary to further address the role of TRPV1 in gastric carcinogenesis.
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页数:11
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