Adam Paul J, Berry Joanne, Loader Julie A, Tyson Kerry L, Craggs Graham, Smith Paul, De Belin Jackie, Steers Graham, Pezzella Francesco, Sachsenmeir Kris F, Stamps Alasdair C, Herath Athula, Sim Edith, O'Hare Michael J, Harris Adrian L, Terrett Jonathan A
Oxford Glycosciences, Abingdon, Oxon, United Kingdom.
Mol Cancer Res. 2003 Sep;1(11):826-35.
Comparative two-dimensional proteome analysis was used to identify proteins differentially expressed in multiple clinical normal and breast cancer tissues. One protein, the expression of which was elevated in invasive ductal and lobular breast carcinomas when compared with normal breast tissue, was arylamine N-acetyltransferase-1 (NAT-1), a Phase II drug-metabolizing enzyme. NAT-1 overexpression in clinical breast cancers was confirmed at the mRNA level and immunohistochemical analysis of NAT-1 in 108 breast cancer donors demonstrated a strong association of NAT-1 staining with estrogen receptor-positive tumors. Analysis of the effect of active NAT-1 overexpression in a normal luminal epithelial-derived cell line demonstrated enhanced growth properties and etoposide resistance relative to control cells. Thus, NAT-1 may not only play a role in the development of cancers through enhanced mutagenesis but may also contribute to the resistance of some cancers to cytotoxic drugs.
采用比较二维蛋白质组分析来鉴定在多种临床正常组织和乳腺癌组织中差异表达的蛋白质。有一种蛋白质,与正常乳腺组织相比,其在浸润性导管癌和小叶癌中的表达升高,该蛋白质为芳胺N - 乙酰转移酶-1(NAT-1),一种II期药物代谢酶。在mRNA水平上证实了NAT-1在临床乳腺癌中的过表达,并且对108名乳腺癌供体的NAT-1进行免疫组织化学分析表明,NAT-1染色与雌激素受体阳性肿瘤密切相关。对正常管腔上皮来源的细胞系中活性NAT-1过表达的影响进行分析表明,相对于对照细胞,其生长特性增强且对依托泊苷具有抗性。因此,NAT-1不仅可能通过增强诱变作用在癌症发展中发挥作用,还可能导致某些癌症对细胞毒性药物产生抗性。