Wang Aijin, Arantes Stacey, Yan Leqin, Kiguchi Kaoru, McArthur Mark J, Sahin Aysegul, Thames Howard D, Aldaz C Marcelo, Macleod Michael C
Department of Carcinogenesis, The University of Texas M D Anderson Cancer Center, Smithville, TX, USA.
BMC Cancer. 2008 Sep 22;8:268. doi: 10.1186/1471-2407-8-268.
Overexpression of the bZip transcription factor, ATF3, in basal epithelial cells of transgenic mice under the control of the bovine cytokeratin-5 (CK5) promoter has previously been shown to induce epidermal hyperplasia, hair follicle anomalies and neoplastic lesions of the oral mucosa including squamous cell carcinomas. CK5 is known to be expressed in myoepithelial cells of the mammary gland, suggesting the possibility that transgenic BK5.ATF3 mice may exhibit mammary gland phenotypes.
Mammary glands from nulliparous mice in our BK5.ATF3 colony, both non-transgenic and transgenic, were examined for anomalies by histopathology and immunohistochemistry. Nulliparous and biparous female mice were observed for possible mammary tumor development, and suspicious masses were analyzed by histopathology and immunohistochemistry. Human breast tumor samples, as well as normal breast tissue, were similarly analyzed for ATF3 expression.
Transgenic BK5.ATF3 mice expressed nuclear ATF3 in the basal layer of the mammary ductal epithelium, and often developed squamous metaplastic lesions in one or more mammary glands by 25 weeks of age. No progression to malignancy was seen in nulliparous BK5.ATF3 or non-transgenic mice held for 16 months. However, biparous BK5.ATF3 mice developed mammary carcinomas with squamous metaplasia between 6 months and one year of age, reaching an incidence of 67%. Cytokeratin expression in the tumors was profoundly disturbed, including expression of CK5 and CK8 (characteristic of basal and luminal cells, respectively) throughout the epithelial component of the tumors, CK6 (potentially a stem cell marker), CK10 (a marker of interfollicular epidermal differentiation), and mIRSa2 and mIRSa3.1 (markers of the inner root sheath of hair follicles). Immunohistochemical studies indicated that a subset of human breast tumors exhibit high levels of nuclear ATF3 expression.
Overexpression of ATF3 in CK5-expressing cells of the murine mammary gland results in the development of squamous metaplastic lesions in nulliparous females, and in mammary tumors in biparous mice, suggesting that ATF3 acts as a mammary oncogene. A subset of human breast tumors expresses high levels of ATF3, suggesting that ATF3 may play an oncogenic role in human breast tumorigenesis, and therefore may be useful as either a biomarker or therapeutic target.
先前已表明,在牛细胞角蛋白-5(CK5)启动子控制下,bZip转录因子ATF3在转基因小鼠的基底上皮细胞中过表达会诱导表皮增生、毛囊异常以及口腔黏膜的肿瘤性病变,包括鳞状细胞癌。已知CK5在乳腺的肌上皮细胞中表达,这表明转基因BK5.ATF3小鼠可能会表现出乳腺表型。
通过组织病理学和免疫组织化学检查了我们的BK5.ATF3群体中未生育小鼠的乳腺,包括非转基因和转基因小鼠。观察未生育和已生育的雌性小鼠是否可能发生乳腺肿瘤,并通过组织病理学和免疫组织化学分析可疑肿块。同样对人乳腺肿瘤样本以及正常乳腺组织进行ATF3表达分析。
转基因BK5.ATF3小鼠在乳腺导管上皮的基底层表达核ATF3,并且在25周龄时,一个或多个乳腺中常常会发生鳞状化生病变。在饲养16个月的未生育BK5.ATF3或非转基因小鼠中未观察到恶性进展。然而,已生育的BK5.ATF3小鼠在6个月至1岁之间发生了伴有鳞状化生的乳腺癌,发病率达到67%。肿瘤中的细胞角蛋白表达受到严重干扰,包括CK5和CK8(分别为基底细胞和管腔细胞的特征性表达)在肿瘤上皮成分中的表达、CK6(可能是干细胞标志物)、CK10(毛囊间表皮分化标志物)以及mIRSa2和mIRSa3.1(毛囊内根鞘标志物)。免疫组织化学研究表明,一部分人乳腺肿瘤表现出高水平的核ATF3表达。
ATF3在小鼠乳腺的CK5表达细胞中过表达会导致未生育雌性小鼠发生鳞状化生病变,在已生育小鼠中发生乳腺肿瘤,这表明ATF3作为一种乳腺癌基因发挥作用。一部分人乳腺肿瘤表达高水平的ATF3,这表明ATF3可能在人乳腺肿瘤发生中起致癌作用,因此可能作为生物标志物或治疗靶点。