Davies Michael P A, O'Neill Penny A, Innes Helen, Sibson D Ross
Clatterbridge Cancer Research Trust, JK Douglas Laboratories, Clatterbridge Hospital, Bebington, Wirral, UK.
Breast Cancer Res. 2005;7(1):R113-8. doi: 10.1186/bcr965. Epub 2004 Nov 23.
Genetic abnormalities or mutations in premalignant breast lesions may have a role in progression toward malignancy or influence the behaviour of subsequent disease. The A908G (Lys303-->Arg) change in the gene encoding oestrogen receptor-alpha (ER-alpha) creates a hypersensitivity to oestradiol and would have significant consequences if present in breast carcinoma, especially those treated with endocrine therapy. We have therefore examined a panel of endocrine-treated invasive carcinomas for the presence of this mutation.
Sequencing of control DNA was shown to detect mutation present in as little as 15% of the starting material. Enrichment for the mutation by using MboII restriction digestion allowed the detection of mutant present at 1% or less. We applied these techniques to genomic DNA and cDNA from 136 invasive breast carcinomas.
No evidence of the A908G mutation was found with either technique. The incidence of this mutation in our panel of tumours is therefore significantly less than previously reported.
The fact that the mutation was not found leads us to believe that this mutation is absent from most cells in invasive carcinomas and furthermore that the major expression product of the ER-alpha gene in cancers does not contain the K303R mutation. It is therefore unlikely to influence the effectiveness of endocrine treatment.
癌前乳腺病变中的基因异常或突变可能在向恶性肿瘤进展过程中起作用,或影响后续疾病的行为。编码雌激素受体α(ER-α)的基因中的A908G(Lys303→Arg)变化会导致对雌二醇超敏,如果存在于乳腺癌中,尤其是接受内分泌治疗的乳腺癌中,将产生重大后果。因此,我们检测了一组接受内分泌治疗的浸润性癌,以确定是否存在这种突变。
对对照DNA进行测序显示,能检测到起始材料中低至15%的突变。通过使用MboII限制性消化富集突变,可检测到含量为1%或更低的突变体。我们将这些技术应用于136例浸润性乳腺癌的基因组DNA和cDNA。
两种技术均未发现A908G突变的证据。因此,我们检测的肿瘤组中该突变的发生率明显低于先前报道。
未发现该突变这一事实使我们相信,浸润性癌的大多数细胞中不存在这种突变,而且癌中ER-α基因的主要表达产物不包含K303R突变。因此,它不太可能影响内分泌治疗的效果。