Negin Raei

Bio: Negin Raei is an academic researcher from University of Tabriz. The author has contributed to research in topics: Helicobacter pylori & Cancer. The author has an hindex of 3, co-authored 7 publications receiving 62 citations. Previous affiliations of Negin Raei include Tehran University of Medical Sciences & University of Mohaghegh Ardabili.

Helicobacter pylori Infection and Dietary Factors Act Synergistically to Promote Gastric Cancer.

Abstract: However, the incidence of gastric cancer (GC) has been decreased in past decades; GC is the second cause of cancer related death in the world. Evidence has illustrated that several factors including Helicobacter pylori (H. pylori) infection, host genetics, and environmental factors (smoking and particularly diet) may play a crucial role in gastric carcinogenesis. It has been demonstrated that high consumption of fresh fruits, vegetables, high level of selenium and zinc in drinking water, sufficient iron, and cholesterol protect against GC, while; smoked , pickled, and preserved foods in salt, and nitrites increase the risk of GC. Epidemiological studies have also proved that H. pylori infection and a high salt diet could independently induce atrophic gastritis and intestinal metaplasia. Recently, studies have been demonstrated that dietary factors directly influence H. pylori virulence. The use of appropriate diet could reduce levels of H. pylori colonization or virulence and prevent or delay development of peptic ulcers or gastric carcinoma. This is attractive from a number of perspectives including those of cost, treatment tolerability, and cultural acceptability. This review will describe new insights into the pathogenesis of H. pylori in relation to environmental factors, especially dietary, not only to find the developed means for preventing and treating GC, but also for understanding the role of chronic inflammation in the development of other malignancies.

Helicobacter pylori cag Pathogenicity Island cagL and orf17 Genotypes Predict Risk of Peptic Ulcerations but not Gastric Cancer in Iran.

Abstract: Background Gastric cancer (GC) is the third most common cancer regarding mortality in the world. The cag pathogenicity island (PAI) of Helicobacter pylori which contains genes associated with a more aggressive phenotype may involve in the pathogenesis of gastrointestinal disease. We here aimed to examine the associations of cagH, cagL, orf17, and cagG genotypes of H. pylori cag PAI with severe gastrointestinal disease. Materials and methods A total of 242 H. pylori strains were genotyped. Histopathological examination and classification of subjects were performed. Results The frequencies of the cagH, cagL, cagG, and orf17 genotypes were 40/54 (74.1%), 53/54 (98.1%), 38/54 (70.4%), and 43/54 (79.6%), respectively, in patients with peptidic ulceration (PU),while in the control group, the frequencies were 87/147 (59.6%) for cagH, 121/146 (82.9%) for cagL, 109/146 (74.7%) for cagG, and 89/146 (61.0%) for orf17. The results of simple logistic regression analysis showed that the cagL and orf17 genotypes were significantly associated with an increased risk of PU not GC; the ORs (95% CI) were 10.950 (1.446-82.935), and 2.504 (1.193-5.253), respectively. No significant association was found between the cagH and cagG genotypes and the risk of both the PU and the GC in Iran (P>0.05). Finally, multiple logistic regression analysis showed that the cagL genotype was independently and significantly associated with the age- and sex-adjusted risk for PU; the OR (95% CI) was 9.557 (1.219-17.185). Conclusions We conclude that the orf17 and especially cagL genotypes of H. pylori cag PAI could be factors for risk prediction of PU, but not GC in Iran.

Active Immunization with Recombinant PilA protein Protects Against Pseudomonas aeruginosa Infection in a Mouse Burn Wound Model.

Abstract: Pseudomonas aeruginosa as an opportunistic human pathogen that causes lethal infections in immunocompromised patients. Type IV pili are critical factors in virulence and colonization of P. aeruginosa in acute burn wound infection. The immunogenicity and efficacy of P. aeruginosa recombinant PilA (r-PilA) was evaluated in an experimental model of burn wound sepsis as a vaccine candidate. In this study, female C57BL/6 mice were divided into five groups. Mice in the experimental groups received either r-PilA vaccine alone or in combination with the alum adjuvant or complete Freund's adjuvant (CFA). Mice in the negative control group received phosphate-buffered saline (PBS). In order to characterize the response of Th1-Th2 to immunization, the cytokine profiles of spleen cells isolated from r-PilA immunized mice were investigated. Total IgG titers and isotopes were measured using ELISA method and finally, in order to study the systemic infection, bacterial titers in the liver, spleen and blood were also determined. Active immunization with r-PilA, which is followed by two booster shots, was sufficient to generate a robust immune response in mice. Cytokine analysis demonstrated the secretion of IL-4 and INF-ɣ from splenocytes in response to in vitro antigen stimulation. The IgG response to r-PilA was a Th2 type response consis¬¬ting predominantly of the isotype IgG1 accompanied by lower levels of IgG2a. In conclusion, in this burned mouse model, vaccination with r-PilA can increase the humoral immunity, thereby leading to an effective protection against P. aeruginosa infection.

Inverse relationship between cagG-positive Helicobacter pylori status and risk of gastric ulcer.

Abstract: Helicobacter pylori is a spiral-shaped gram-negative bacterium that infects the human gastric mucosa and is associated with the development of gastrointestinal diseases such as chronic atrophic gas...

Stem Cells,Cancer and Cancer Stem Cells

Abstract: Stem cells are defined as cells able to both extensively self-renew and differentiate into progenitors. Research data show that more resistant stem cells than common cancer cells exist in cancer patients.To identify unrecognized differences between cancer stem cells and cancer cells might be able to develope effective classification,diagnose and treat ment for cancer.

Gastric cancer: Metabolic and metabolomics perspectives (Review)

Abstract: Gastric cancer is one of the most malignant tumors worldwide and remains a major health threat in Asia-Pacific regions, while its pathological mechanism is generally unknown Recent research has advanced the understanding of the relationship between metabolic reprogramming and carcinogenesis In particular, metabolic regulation and cancer research are being further brought into sharp focus with the emergence of metabolomics Not only can metabolomics provide global information on metabolic profiles of specific tumors, but it can also act as a promising tool to discover biomarkers regarding diagnosis, metastatic surveillance and chemotherapeutic sensitivity prediction Meanwhile, metabolism-based anticancer therapies will be further discovered Up to now, accumulative studies have highlighted the application of metabolomics in gastric cancer research regarding different aspects; therefore we summarized the current available results of how metabolic changes are linked to gastric carcinogenesis, and how metabolomics holds promise for the diagnosis, metastatic surveillance, treatment and prognosis prediction of gastric cancer