Anderson T I, Wooster R, Laake K, Collins N, Warren W, Skrede M, Elles R, Tveit K M, Johnston S R, Dowsett M, Olsen A O, Møller P, Stratton M R, Børresen-Dale A L
Department of Genetics, Norwegian Radnon Hospital, Oslo, Norway.
Hum Mutat. 1997;9(6):531-6. doi: 10.1002/(SICI)1098-1004(1997)9:6<531::AID-HUMU6>3.0.CO;2-4.
In the present study, leukocyte DNA from 143 patients with familial clustering of breast and/or ovarian cancer and tumour DNA from 96 breast carcinomas were screened for base mutations in the estrogen receptor gene (ESR). Three patients with a family history of cancer were carrying a Gly160Cys germline substitution. This alteration was also detected in eight (four females and four males) of 729 controls (366 female, 363 males), indicating that the substitution probably represents a polymorphism. However, in the 229 female controls in whom family history of cancer was known, one of two who had a sister with breast cancer was carrying the variant allele. Hence, a possible clinical significance of the glycine into cysteine cannot be completely ruled out and should be further investigated. Somatic mutations were not detected in any of the tumours studied, and the present data do not provide support for somatic ESR base mutations as an important mechanism for hormonal therapy resistance in estrogen receptor-positive breast carcinomas.
在本研究中,对143例有乳腺癌和/或卵巢癌家族聚集性患者的白细胞DNA以及96例乳腺癌的肿瘤DNA进行了雌激素受体基因(ESR)碱基突变筛查。3例有癌症家族史的患者携带Gly160Cys种系替代突变。在729名对照者(366名女性、363名男性)中的8人(4名女性和4名男性)也检测到了这种改变,表明该替代突变可能代表一种多态性。然而,在229名已知有癌症家族史的女性对照者中,有一个姐姐患乳腺癌的两人中有一人携带变异等位基因。因此,不能完全排除甘氨酸突变为半胱氨酸的可能临床意义,应进一步研究。在所研究的任何肿瘤中均未检测到体细胞突变,目前的数据不支持体细胞ESR碱基突变是雌激素受体阳性乳腺癌激素治疗耐药的重要机制这一观点。