The incidence of Cancer is still increasing worldwide, specially, at an alarming rate in the developing countries and remain one of the major cause of morality worldwide. The role of different antioxidants, both in fruits and vegetable and in synthetic form as chemo-preventive measure is now well established from different studies. The incidence of cancer is lower in those countries where the traditional diet provides plenty of antioxidants. The aim of this study is to evaluate standard modalities of patients with different neoplastic diseases. Three identically designed, open and multi-centric studies were conducted at the same time in Bangladesh in 2008-2009. Efficacy of antioxidant rich product, Oncoxin, in head and throat, breast and uterine cervix cancer, when administered with conventional oncologic therapy Each study included 30 patient couples with similar stages of cancer. One patient of each couple received the standard treatment for their stage (reference group). The other (experimental group) also received Oncoxin for 365 days. The result gathered in the 3 studies showed that the administration of Oncoxin led to a significant improvement of the quality of life of patients, fewer episodes of depression and increased optimism. These patients handled better the radiotherapy and chemotherapy sessions with fewer and less intense adverse reactions. During the final visit, it was observed a 59.26% increase in the Karnofsky index in the experimental group compared to 30.38% in the reference group, and a 16.05% drop (76.93% due to deaths) in the experimental group for 39.24% (64.52% due to deaths) in the reference group. Survival rates were greater in the experimental group in all three studies (87.65% versus 74.68%). The treatment with ONCOXIN Solution proves its effectiveness as a treatment modality associated with complex oncological treatment, the short and medium terms.TAJ 2009; 22(1): 172-175
Tobacco consumption in various forms is one of the major risk factor for the development of head and neck squamous cell carcinoma. Polymorphisms in XRCC1 and XRCC2 genes may alter an individual's susceptibility to tobacco-related cancers. Here, we have investigated the interaction of XRCC1 (Arg399Gln) and XRCC2 (Arg188His) polymorphism and tobacco exposure in the progression of HNSCC in northeast Indian population. The population-based case-control study includes 110 HNSCC patients and 140 controls. The polymorphisms of XRCC1 and XRCC2 were studied by means of PCR-RFLP, and the results were confirmed by DNA sequencing. Smokers and tobacco-betel quid chewers were significantly higher in cases (P = 0.045 and 0.033). The variant homozygote AA genotype of XRCC1 Arg399Gln and heterozygote GA genotype of XRCC2 Arg188His has an increased risk toward HNSCC (OR 2.43; P = 0.031 and OR 3.29; P < 0.01, respectively). The interaction between tobacco-betel quid chewing and variant genotypes of XRCC1 and XRCC2 resulted in several fold increase the risk of HNSCC, when compared to non-chewers. Heavy smokers carrying XRCC1 AA and XRCC2 GA genotypes had a significantly higher risk of HNSCC compared to never smokers (P = 0.017 and 0.003, respectively). Upon gene-gene interaction analysis, individuals carrying both XRCC1 GA (Arg/Gln) and XRCC2 GA (Arg/His) genotypes had the highest risk of HNSCC (P = 0.001).Our finding suggests that interaction of tobacco and polymorphisms of XRCC1 and XRCC2 increases the risk of HNSCC. Furthermore, cross talk between these two DNA repair genes might modulate susceptibility toward HNSCC.
Genetic polymorphisms in tobacco-metabolizing genes may modulate the risk of head and neck cancer (HNC). In Northeast India, head and neck cancers and tobacco consumption remains most prevalent. The aim of the study was to investigate the combined effect of cytochrome P450 1A1 (CYP1A1) T3801C, glutathione S-transferases (GSTs) genes polymorphisms and smoking and tobacco-betel quid chewing in the risk of HNC. The study included 420 subjects (180 cases and 240 controls) from Northeast Indian population. Polymorphisms of CYP1A1 T3801C and GST (M1 & T1) were studied by polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) and multiplex PCR, respectively. Logistic regression (LR) and multifactor dimensionality reduction (MDR) approach were applied for statistical analysis. LR analysis revealed that subjects carrying CYP1A1 TC/CC + GSTM1 null genotypes had 3.52-fold (P < 0.001) increase the risk of head and neck squamous cell carcinoma (HNSCC). Smokers carrying CYP1A1 TC/CC + GSTM1 null and CYP1A1 TC/CC + GSTT1 null genotypes showed significant association with HNC risk (odds ratio [OR] = 6.42; P < 0.001 and 3.86; P = 0.005, respectively). Similarly, tobacco-betel quid chewers carrying CYP1A1 TC/CC + GSTM1 null genotypes also had several fold increased risk of HNC (P < 0.001). In MDR analysis, the best model for HNSCC risk was the four-factor model of tobacco-betel quid chewing, smoking, CYP1A1 TC/CC, and GSTM1 null genotypes (testing balance accuracy [TBA] = 0.6292; cross-validation consistency [CVC] = 9/10 and P < 0.0001). These findings suggest that interaction of combined genotypes of carcinogen-metabolizing genes with environmental factors might modulate susceptibility of HNC in Northeast Indian population.
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