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Oncogenomics of Mesothelioma in Humans

机译:人间皮瘤的肿瘤基因组学

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Beginning in 1990, the Human Genome Project broughtabout a significant breakthrough in medical genetics andapplication of genetic knowledge in common diseases. Ithas revolutionized the traditional medical concept thatgenetics is involved only in extremely rare inherited diseases,to the new concept that genetic factors significantlycontribute to the mechanism and progression of mostdiseases, as well as the response and side effects of thetreatment. [1] Cancer is the best example to demonstratethe benefits of genetic knowledge. It is universallyaccepted that cancer is a genetic disorder that results inabnormal cell growth and invasiveness with the potentialto spread to other parts of the body. Better understandingof cancer genetics leads to new types of cancer diagnostictests and several novel drugs which are designed to targetspecific genetic abnormalities in cancer. Many patientswho are suffering from various cancers, such as leukemia,breast cancer and lung cancer, are now having bettertreatment outcomes, longer life expectancy and sufferingless adverse effects from treatment with those targetedtherapies.
机译:从1990年开始,人类基因组计划在医学遗传学和常见疾病的遗传学知识应用方面取得了重大突破。它彻底改变了遗传学仅涉及极少见的遗传疾病的传统医学观念,将遗传因素显着促进大多数疾病的机理和进程以及治疗的反应和副作用的新观念转变了。 [1]癌症是证明遗传知识益处的最好例证。癌症是一种遗传疾病,会导致异常的细胞生长和侵袭性,并有可能扩散到身体的其他部位,这已被普遍接受。对癌症遗传学的更好理解导致了新型的癌症诊断测试和旨在针对癌症中特定遗传异常的几种新型药物。现在,许多患有各种癌症(例如白血病,乳腺癌和肺癌)的患者因采用这些靶向疗法进行治疗而具有更好的治疗效果,更长的预期寿命和无痛苦的副作用。

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