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原位乳腺癌与微嵌合体。

In situ breast cancer and microchimerism.

作者信息

Eun Jinny K, Guthrie Katherine A, Zirpoli Gary, Gadi V K

机构信息

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

出版信息

Sci Rep. 2013;3:2192. doi: 10.1038/srep02192.

Abstract

Microchimeric cells of fetal origin persistent in the maternal circulation post-partum are associated with protection against invasive breast cancer. Here using quantitative genomic methods, we evaluated for the presence of male fetal microchimerism in buffy coat cells from women with a prior history of breast carcinomas in situ (CIS) and in healthy controls. Fetal microchimerism was detected in 75 of 88 controls (85%) and in 57 of 89 CIS patients (64%). The odds ratio for protection against non-invasive breast disease was 0.26 (95% confidence interval 0.12-0.56; p < 0.001 adjusted for age and body mass index). Similar to women with invasive breast cancer, women with CIS who are naturally at high risk for future invasive disease were deficient for fetal microchimerism. In addition to autologous anti-tumor immune responses, the maintenance of haploidentical microchimerism may impart an allogeneic edge in immunosurveillance.

摘要

产后持续存在于母体循环中的胎儿来源的微嵌合细胞与预防浸润性乳腺癌有关。在此,我们使用定量基因组方法,评估了有原位乳腺癌(CIS)病史的女性和健康对照者的血沉棕黄层细胞中男性胎儿微嵌合体的存在情况。在88名对照者中有75名(85%)检测到胎儿微嵌合体,在89名CIS患者中有57名(64%)检测到。预防非浸润性乳腺疾病的优势比为0.26(95%置信区间0.12 - 0.56;根据年龄和体重指数调整后p < 0.001)。与浸润性乳腺癌女性相似,未来有侵袭性疾病自然高风险的CIS女性缺乏胎儿微嵌合体。除了自体抗肿瘤免疫反应外,单倍体微嵌合体的维持可能在免疫监视中赋予异基因优势。

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