首页> 外文期刊>British Journal of Dermatology >Naevus count and MC1R R MC1R R alleles contribute to melanoma risk
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Naevus count and MC1R R MC1R R alleles contribute to melanoma risk

机译:Naevus Count和MC1R R MC1R R等位基因有助于黑色素瘤风险

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Summary Melanoma is the most dangerous form of skin cancer: around 15% of cases worldwide are fatal, but with early detection, survival rates are better than 95%. Having many large moles or having red hair increases a person's risk of developing melanoma; having certain versions of the MC1R gene, called R alleles, the main cause of red hair, also increases melanoma risk. This study, from Australia, aimed to find out if having both those risk factors increased melanoma risk more than the two risk levels simply added together. 611 people with melanoma and 656 who had never had melanoma donated a DNA sample, and researchers recorded the number of large moles, their skin and eye colour, and hair colour at age 21. The authors found that people with red hair and 20+ large moles were 10 times more likely to have melanoma than people with 0‐4 moles and dark brown hair. Looking specifically at the types of the MC1R gene that people carried, people with 20+ moles and MC1R R/R genotype were 25 times more likely to have melanoma than people with 0‐4 moles and MC1R wildtype/wildtype (consensus) genotype. While the R/R genotype, with or without the red hair phenotype, and a high mole count are both strong melanoma risk factors on their own, when combined they result in an extremely high‐risk profile for melanoma. The absolute lifetime risk to age 75 of getting melanoma in Australia is 23.3% for men and 19.3% for women who have 20+ moles and MC1R R/R genotype, compared to just 0.8% for men and 0.7% for women with 0‐4 moles and MC1R wildtype/wildtype genotype. This is higher than the risk threshold for screening in other cancers, so the authors suggest that people with many moles and red hair should be regularly checked for melanoma by a doctor, and that people with many moles but non‐red hair should also be checked to determine if they have an MC1R R/R genotype.
机译:摘要黑素瘤是最危险的皮肤癌症形式:大约15%的全世界病例是致命的,但随着早期发现,生存率优于95%。拥有许多大痣或红头发会增加一个人发展黑素瘤的风险;具有某些版本的MC1R基因,称为R等位基因,红发的主要原因,也增加了黑色素瘤的风险。来自澳大利亚的这项研究旨在发现具有这些风险因素的危险因素增加了黑色素瘤的风险超过了两个风险水平,只需一起添加两个风险。 Melanoma和656人的611人从未患过黑素瘤捐赠了DNA样本,研究人员在21岁时记录了大摩尔,皮肤和眼睛颜色的大量,头发颜色。作者发现,红发的人和20多个大Moles比用0-4摩尔和深棕色的毛发的人更容易获得黑素瘤的10倍。特别是在携带人们携带的MC1R基因的类型中,具有20多个痣和MC1R R / R基因型的人比0-4摩尔和MC1R野生型/野生型(共有)基因型(共有)基因型的人更可能产生25倍。虽然R / R基因型,有或没有红发表型,并且高痣计数都是强烈的黑色素瘤风险因素,当时它们导致黑色素瘤的极高风险概况。澳大利亚Melanoma年龄75岁的绝对寿命风险为23.3%,男性和20毫米且MC1R R / R基因型的女性为19.3%,而男性为0.8%,女性为0-4的女性为0.7% Moles和MC1R野生型/野生型基因型。这高于其他癌症筛查的风险阈值,因此作者表明,应该通过医生定期检查有许多痣和红发的人,并且还应该检查许多痣但非红发的人确定它们是否具有MC1R R / R基因型。

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