Can histone epigenetic profiling become an alternative treatment modality for colon cancer

T. Pillai
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Abstract

Colorectal cancer (CRC) is a formidable health problem worldwide. Almost 60% of cases are encountered in developed countries. In India, the annual incidence rates (AARs) for colon cancer in men are 4.4 per 100000. The AAR for colon cancer in women is 3.9per 100000 (GLOBO. CAN 2008). There were marked developments in the chemotherapy of CRC in the last decade. Eight new drugs were approved for chemotherapy. The survival has doubled compared to 5-fluorouracil alone. KRAS testing opened an era of personalised therapy. Though on an average there are 90 genes mutated per cancer, only less than 20 pathways will actually drive cancer development. The available therapy with combinations for CRC is very expensive coming to $300000 for 24 months. Early detection of tumors and improved therapy has lead to improvement in survival. With the administration of the adjuvant 5-fluorouracil, an improvement in survival of approximately 30%, with an additional 20% improvement with the addition of oxaliplatin in stage III colon cancer is reported. Family history of CRC contributes only 25% thus most commonly occurs sporadically, suggesting a contribution for shared genes and environment. About 5-% are from inherited mutations, while the remaining of the familial forms results from gene environment interactions.
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组蛋白表观遗传分析能否成为结肠癌的一种替代治疗方式
结直肠癌(CRC)是一个全球性的严重健康问题。近60%的病例发生在发达国家。在印度,男性结肠癌的年发病率(AARs)为每10万人4.4例。女性结肠癌的AAR是3.9 / 100000 (GLOBO)。可以2008)。近十年来,结直肠癌的化疗有了显著的发展。8种新药获批用于化疗。与单独使用5-氟尿嘧啶相比,生存率提高了一倍。KRAS测试开启了个性化治疗的时代。虽然每种癌症平均有90个基因突变,但实际上只有不到20个途径会导致癌症的发展。现有的联合治疗结直肠癌的费用非常昂贵,24个月需要30万美元。早期发现肿瘤和改进治疗导致生存率的提高。据报道,在给予5-氟尿嘧啶辅助治疗后,III期结肠癌患者的生存率提高了约30%,在添加奥沙利铂的情况下,生存率又提高了20%。CRC家族史仅占25%,因此最常见的是零星发生,提示共享基因和环境的贡献。大约5%来自遗传突变,而其余的家族性形式来自基因与环境的相互作用。
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