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Hypofolatemia as a risk factor for head and neck cancer.

机译:低叶酸血症是头颈癌的危险因素。

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Head and neck cancer (HNSCC) includes squamous cell carcinomas of the oral cavity, pharynx and larynx. Approximately 38,500 cases of HNSCC are estimated to occur in the USA in 2004, with 11,000 deaths. HNSCCs represent about 3% of all malignant tumors in the USA. However, in other parts of the world, as India, Southeast Asia or Brazil, the disease is much more prevalent. The standard therapeutic approach, focused on surgery, irradiation and chemotherapy, alone or in combination, has been in part modified in the last 30 years, but the overall survival of HNSCC patients has not substantially improved. To characterize and thus identify high-risk mucosal areas and preclinical tumors, molecular abnormalities in head and neck carcinogenesis have been extensively studied. Metabolic aspects in head and neck carcinogenesis have been less extensively studied. Nevertheless, we know that metabolic alterations, often aspecific, are frequently associated with cancer. These may be secondary or may precede tumor development and favorite progression. In particular, based upon our results, a role for folate deficiency as a risk factor in head and neck carcinogenesis seems plausible. A chemoprevention protocol with folate is at present feasible and ethically correct and is already in progress at our institution. Homocysteine levels in cancer patients are probably largely affected by the HNSCC phenotype. An accumulation of homocysteine might reveal a genetic defect which is theoretically a target for pharmacological therapy, for example by antifolic drugs.
机译:头颈癌(HNSCC)包括口腔,咽和喉的鳞状细胞癌。据估计,2004年美国大约发生38,500例HNSCC病例,死亡11,000人。在美国,HNSCC约占所有恶性肿瘤的3%。但是,在世界其他地区,例如印度,东南亚或巴西,该病更为普遍。在过去的30年中,针对单独,或结合手术,放疗和化疗的标准治疗方法进行了部分修改,但是HNSCC患者的总体生存率并未得到实质性改善。为了表征并确定高风险的粘膜区域和临床前肿瘤,已对头颈部致癌作用中的分子异常进行了广泛研究。头部和颈部癌变过程中的代谢方面尚未得到广泛研究。然而,我们知道,代谢变化(通常是非特异性的)经常与癌症相关。这些可能是继发性的,也可能在肿瘤发展和最喜欢的进展之前。特别是,根据我们的研究结果,叶酸缺乏作为头颈部癌变危险因素的作用似乎是合理的。目前,叶酸的化学预防方案是可行的,并且在伦理上是正确的,并且已经在我们机构进行中。癌症患者的同型半胱氨酸水平可能在很大程度上受到HNSCC表型的影响。同型半胱氨酸的积累可能揭示遗传缺陷,这在理论上是药理学治疗的目标,例如抗叶酸药物。

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