A pilot study of the impact of Vitamin C supplementation with neoadjuvant chemoradiation on regulators of inflammation and carcinogenesis in esophageal cancer patients

被引:13
作者
Abdel-Latif, Mohamed M. M. [1 ,2 ]
Babar, Mawash [2 ]
Kelleher, Dermot [3 ]
Reynolds, John V. [2 ,4 ]
机构
[1] Assiut Univ, Dept Clin Pharm, Fac Pharm, Assiut, Egypt
[2] St James Hosp, Trinity Ctr Hlth Sci, Dept Clin Surg, Dublin 8, Ireland
[3] St James Hosp, Trinity Ctr Hlth Sci, Dept Clin Med, Dublin, Ireland
[4] Trinity Coll Dublin, Dublin 8, Ireland
关键词
Cytokines; esophageal cancer; neoadjuvant chemoradiation; nuclear factor-kappa B; Vitamin C; NF-KAPPA-B; NEOPLASTIC PROGRESSION; BARRETTS-ESOPHAGUS; GASTRIC CARDIA; ADENOCARCINOMA; RISK; ANTIOXIDANT; PREVENTION; CELLS; INHIBITION;
D O I
10.4103/jcrt.JCRT_763_16
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Aims: Vitamin C plays a role in chemoprevention in cancer treatment, and Vitamin C modulates many regulators of inflammation in in vitro studies. The aim of this study is to assess the effect of Vitamin C supplementation with neoadjuvant chemoradiation in esophageal adenocarcinoma on the nuclear factor-kappa B (NF-kappa B) and associated cytokines. Materials and Methods: A total of 20 patients undergoing multimodal treatment for esophageal adenocarcinoma were randomized to receive Vitamin C (1000 mg/day) orally for 4 weeks or no supplementation. Pre-and post-Vitamin C endoscopic biopsies were used for the study of NF-kappa B activity and cytokine analysis. Results: NF-kappa B activity along with cytokines was activated in the cancer tissue pretreatment. Down-regulation in NF-kappa B activity was observed in 25% of cases, two from the Vitamin C arm posttreatment. There was a significant reduction in cytokines levels in the cancer group, and this effect was more pronounced in the Vitamin C group (P < 0.05). Conclusions: Vitamin C supplementation had a mild protective effect in modulating of regulators of inflammation and carcinogenesis. Further studies with larger numbers of endpoints are needed to evaluate its effect on modulation of chemoradiation responses.
引用
收藏
页码:185 / 191
页数:7
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