首页> 外文期刊>Japanese journal of clinical oncology. >Recent progress in carcinogenesis, progression and therapy of breast cancer: the 20th Hiroshima Cancer Seminar--the 4th Three Universities' Consortium International Symposium, October 2010: 31 October 2010, International Conference Center Hiroshima.
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Recent progress in carcinogenesis, progression and therapy of breast cancer: the 20th Hiroshima Cancer Seminar--the 4th Three Universities' Consortium International Symposium, October 2010: 31 October 2010, International Conference Center Hiroshima.

机译:乳腺癌的致癌,进展和治疗的最新进展:第20届广岛癌研讨会-第四届三大大学联盟国际研讨会,2010年10月:2010年10月31日,广岛国际会议中心。

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The 20th Hiroshima Cancer seminar focused upon breast cancer research and treatment particularly on the mechanism of tumorigenesis and drug resistance and development of novel therapeutics. Several molecules such as retinoblastoma and p16 were raised as key factors in tumorigenesis and invasiveness. Estrogen-related pathways seem to be closely involved in the process. For the tumor lacking hormone receptor and human epidermal growth factor 2, some other mechanisms could be responsible. It seems that MicroRNA 22 directing some putative targets such as SIRT1, Sp1 and CDK6 plays a crucial role in breast tumor growth and metastasis. In addition, ribophorin and the associated molecules might be engaged in breast cancer stemness. Obviously, these molecules provide potential for therapeutic targets. It was also discussed about new drug development such as anti-human epidermal growth factor 2 therapy, anti-angiogenesis, pro-tumor aspects of anti-cancer therapy and application of circulating markers for monitoring, imaging and health-care system. Furthermore, we discussed risk factors, prevention and screening to reduce invasive cancers as well. Throughout the conference, panelists and attendee indicated the importance of translational research and biomarker exploration in order to realize efficient and individualized therapy for breast cancer.
机译:第20届广岛癌症研讨会的重点是乳腺癌的研究和治疗,尤其是肿瘤发生和耐药的机制以及新型疗法的开发。诸如视网膜母细胞瘤和p16的几种分子被提出作为肿瘤发生和侵袭性的关键因素。雌激素相关途径似乎与该过程密切相关。对于缺乏激素受体和人类表皮生长因子2的肿瘤,其他一些机制可能是负责任的。似乎指导某些假定靶标(如SIRT1,Sp1和CDK6)的MicroRNA 22在乳腺肿瘤的生长和转移中起着至关重要的作用。另外,核糖蛋白和相关分子可能参与了乳腺癌的干性。显然,这些分子为治疗靶标提供了潜力。还讨论了新药的开发,例如抗人类表皮生长因子2治疗,抗血管生成,抗癌治疗的肿瘤前体以及循环标记物在监测,成像和医疗保健系统中的应用。此外,我们还讨论了风险因素,预防和筛查以减少浸润性癌症。在整个会议期间,小组成员和与会者指出了转化研究和生物标记物探索的重要性,以实现高效,个性化的乳腺癌治疗。

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