Nemzeti Gyógyszerkutatási és Fejlesztési Laboratórium (PharmaLab)(RRF-2.3.1-21-2022-00015)
Támogató: NKFIH
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.