Expression of Cancer Stem Cell Marker CD44 and Its Polymorphisms in Patients with Chronic Gastritis, Precancerous Gastric Lesion, and Gastric Cancer: A Cross-Sectional Multicenter Study in Thailand. (27th December 2017)

• Record Type: Journal Article
• Authors: Tongtawee, Taweesak; Wattanawongdon, Wareeporn; Simawaranon, Theeraya; Kaewpitoon, Soraya; Kaengpenkae, Sivamate; Jintabanditwong, Nichaphat; Tangjanyatham, Pakorn; Ratchapol, Warisara; Kangwantas, Kokiet; Dechsukhum, Chavaboon; Leeanansaksiri, Wilairat; Kaewpitoon, Natthawut; Matrakool, Likit; Panpimanmas, Sukij
• Other Names: Mahady Gail B. Academic Editor.
• Is Part Of: BioMed research international. Volume 2017(2017)
• Publication Date: 2017-12-27
• Subjects: Medicine -- Periodicals; Biology -- Periodicals; Biotechnology -- Periodicals; Life sciences -- Periodicals; 610.5
• DOI: 10.1155/2017/4384823
• Languages: English
• ISSNs: 2314-6133

Abstract

Abstract : Here we investigated CD44 protein expression and its polymorphisms in patients with chronic gastritis, precancerous gastric lesions, and gastric cancer; and we evaluated our result with the risk of CD44 protein expression and clinicopathological characteristics. Our results obtained by analyzing 162 gastric cancer patients, 125 chronic gastritis, and 165 precancerous gastric lesions from three study centers in Thailand showed that CD44 expression was significantly higher in patients with precancerous gastric lesions and gastric cancer while patients with chronic gastritis were negative for CD44 staining (p = 0.036 ). We further observed the significant association of variant genotype; gastric cancer patients carrying AG or GG of CD44 rs187116 had more increased risk of CD44 expression than wild-type (WT) carriers (AG: odds ratio (OR) = 5.67; 95% CI = 1.57–7.23; p = 0 . 024 and GG: OR = 8.32; 95% CI = 2.94–11.42; p = 0 . 016 ), but no significant difference in the risk of CD44 expression due to polymorphism in patients with precancerous gastric lesions. Our results suggested that CD44 expression could be used as a marker for the prediction of gastric cancer development, particularly in patients with precancerous gastric lesions carrying AG or GG, who were selected to surveillance follow-up for gastric cancer prevention.