pylori isolates. Notably, peptidyl-prolyl cis–trans isomerase (PPIase) was detected positively in 11 out of 22 (50%) gastric cancer-associated H. pylori strains. In contrast, <24% of the H. pylori strains from superficial gastritis showed positive results. Given the potential role of PPIases in cell growth, apoptosis and oncogenic transformation, our results suggest that PPIase may represent a novel marker and potential therapeutic target for gastric cancer. Helicobacter pylori is a microaerophilic Gram-negative

bacillus that colonizes the stomach in more than half of the world’s population (Parsonnet, 1995). It is the causative agent of chronic gastritis and contributes to peptic ulcer. There is strong evidence www.selleckchem.com/products/abt-199.html to indicate that H. pylori plays an important role in the pathogenesis of noncardia gastric cancer Group HaCC (2001). Once infected by this bacterium, the clinical outcome depends on the interaction of virulent effects of the bacterium, the host response and the environment. DNA fingerprinting studies revealed considerable diversity among independent H. pylori isolates (Akopyanz et al., 1992). This observation was supported by later studies using multilocus enzyme electrophoresis analysis (Go et al., 1996) and restriction fragment length polymorphisms analysis Ceritinib solubility dmso (Salaun et al., 1998). Genes that are present in one

strain and absent or substantially different in the others can be of significant biological interest. The CagA protein was one of the first several virulent determinants and disease markers identified in H. pylori. Previous studies have demonstrated that strains lacking the cagA gene, which are common in Europe and North America, are rarely implicated in overt disease (Mimuro et al., 2008). Patients with high titers of anti-CagA antibodies tend to have a higher risk of developing peptic ulcer or gastric cancer (Covacci et al., 1993). The genetic heterogeneity of H. pylori is believed to be geographical and may occur via DNA rearrangement and the introduction and deletion of foreign sequences (Achtman & Suerbaum, 2000). In

contrast to H. pylori strains from Western countries, most East Asian strains express CagA (Yamaoka et al., 2008). Furthermore, heterogeneity within CagA exists between strains from Western and East Asian countries (Yamaoka Endonuclease et al., 2000). The number of EPIYA-C repeat motifs in the C-terminus of CagA may be related to high incidences of gastric cancer, and thus, is proposed as a marker for clinical outcomes (Yamaoka et al., 1998). In an attempt to identify gastric cancer-specific H. pylori genes, we isolated H. pylori from both gastric cancer patients and superficial gastritis patients, and constructed a gastric cancer-specific gene library using a well-established suppression subtractive hybridization (SSH) method to selectively amplify target DNA fragments and simultaneously suppress nontarget DNA amplification (Diatchenko et al., 1996; Akopyants et al., 1998).