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A common environmental carcinogen unduly affects carriers of cancer mutations: carriers of genetic mutations in a specific protective response are more susceptible to an environmental carcinogen.

机译:常见的环境致癌物过度影响癌症突变的携带者:特定保护性反应中的遗传突变携带者更容易受到环境致癌因素的影响。

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摘要

One way an inherited cancer gene mutation may target specific tissues for cancer is by increasing susceptibility when a tissue is exposed to environmental carcinogens. An example of this may be the increased susceptibility of BRCA1 or BRCA2 mutation carriers to the carcinogen formaldehyde. Formaldehyde is now a proven cause of human myeloid leukemias. Yet millions of tons of formaldehyde are produced every year and it is everywhere. High formaldehyde levels can overwhelm normal enzyme detoxification systems and cause DNA damage. It is known that some types of formaldehyde-associated DNA damage require error-free DNA repairs mediated by pathways containing BRCA1 and BRCA2 proteins. Otherwise some formaldehyde-related DNA damage cannot be properly repaired so mutations may occur. Therefore, carriers of BRCA1 and BRCA2 gene defects should be unduly susceptible to myeloid leukemia. Studies show that inherited biallelic BRCA2 gene defects dramatically increase risks for myeloid leukemia. Heterozygous BRCA1 or BRCA2 mutations also increase risks for myeloid leukemias in 11 of 12 relevant studies. BRCA1/2 mutation carriers may reduce risks for myeloid leukemias by using available precautions to lower their exposure to formaldehyde.
机译:当组织暴露于环境致癌物时,遗传的癌症基因突变可以靶向特定癌症的一种方法是增加敏感性。例如,BRCA1或BRCA2突变携带者对致癌物甲醛的敏感性增加。现在,甲醛已被证明是人类骨髓性白血病的病因。但是,每年都会产生数百万吨的甲醛,并且无处不在。高甲醛含量会使正常的酶解毒系统不堪重负,并造成DNA损伤。众所周知,某些类型的甲醛相关的DNA损伤需要无错误的DNA修复,该修复由包含BRCA1和BRCA2蛋白的途径介导。否则,一些与甲醛有关的DNA损伤将无法正确修复,因此可能发生突变。因此,BRCA1和BRCA2基因缺陷的携带者应该对髓样白血病过度敏感。研究表明,遗传的双等位基因BRCA2基因缺陷极大地增加了髓样白血病的风险。在12项相关研究中的11项中,杂合子BRCA1或BRCA2突变也增加了髓样白血病的风险。 BRCA1 / 2突变携带者可以通过使用现有的预防措施来降低其暴露于甲醛的风险,从而降低骨髓性白血病的风险。

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