Russo J, Reina D, Frederick J, Russo I H
Department of Pathology, Michigan Cancer Foundation, Detroit 48201.
Cancer Res. 1988 May 15;48(10):2837-57.
In order to determine whether human breast epithelial cells undergo malignant transformation when treated with chemical carcinogens in vitro, and how host factors, such as degree of gland development, affect their response to that treatment, twenty-two reduction mammoplasty specimens from women ranging in age from 18 to 63 years and with different parity history were studied in their morphology and in their response to carcinogen treatment in vitro. Fixed tissues were processed for whole mount preparations; it was found that the lobules of the nonpregnant or resting breast tissue could be classified into three types based upon their size and number of alveolar buds composing each one of them, lobules type 1 being the least and lobules type 3 the most differentiated ones. Breast tissues were classified according to the relative proportion of lobules composing it and the reproductive and clinical history of the patient into groups A, B, or C. Fresh tissues from these three groups were digested for obtention of mammary epithelium organoids, which were plated in Dulbecco's minimal essential medium:Ham's F12 (1:1), with 5% horse serum to enhance attachment. When they reached confluence, the cells were replated in serum-free medium; 48 h postplating they were treated with 1.0 microgram/ml 7,12-dimethylbenz(a)anthracene for 24 h, or with 1.0 microgram/ml N-methyl-nitrosourea for 3 h. At every passage, the cells were monitored for colony formation efficiency, survival efficiency in agar-methocel, multinucleation assay, karyotyping, immunocytochemical detection of tumor associated antigens, lectin reactivity, and tumorigenic assay by injection into nude mice. By the fourth passage after treatment, both carcinogens induced increased survival, colony formation in agar-methocel, multinucleation, and increased reactivity with the tumor associated antigen B1:1, an epitope of carcinoembryonic antigen, and the lectins concanavalin A, Dolichos biflorus, and soybean agglutinin. This response was observed only in human breast epithelial cells obtained from less differentiated breasts (Groups A and B), whereas human breast epithelial cells from breasts exhibiting good lobular development (Group C) did not exhibit those changes. No karyotypic abnormalities were detected in treated cells, and they failed to induce tumors when injected into nude mice. It was concluded that mammary gland development is independent of age but is strongly influenced by both the reproductive and clinical history of the donor.(ABSTRACT TRUNCATED AT 400 WORDS)
为了确定人乳腺上皮细胞在体外经化学致癌物处理后是否会发生恶性转化,以及宿主因素(如腺体发育程度)如何影响其对该处理的反应,研究了22份来自年龄在18至63岁、妊娠史不同的女性的缩乳术标本的形态学及其在体外对致癌物处理的反应。对固定组织进行整装制片;发现未孕或静止乳腺组织的小叶可根据其大小和组成每个小叶的腺泡芽数量分为三种类型,1型小叶分化程度最低,3型小叶分化程度最高。根据组成乳腺组织的小叶相对比例以及患者的生育和临床病史,将乳腺组织分为A、B或C组。对这三组的新鲜组织进行消化以获得乳腺上皮类器官,将其接种于含5%马血清的杜氏改良伊格尔培养基:哈姆F12(1:1)中以增强贴壁。当细胞达到汇合时,将其重新接种于无血清培养基中;接种后48小时,用1.0微克/毫升的7,12 - 二甲基苯并(a)蒽处理24小时,或用1.0微克/毫升的N - 甲基 - N - 亚硝基脲处理3小时。在每次传代时,监测细胞的集落形成效率、在琼脂 - 甲基纤维素中的存活效率、多核化测定、核型分析、肿瘤相关抗原的免疫细胞化学检测、凝集素反应性以及通过注射到裸鼠体内进行致瘤性测定。处理后传至第四代时,两种致癌物均诱导细胞存活增加、在琼脂 - 甲基纤维素中形成集落、多核化增加,以及与肿瘤相关抗原B1:1(癌胚抗原的一个表位)、伴刀豆球蛋白A、双花扁豆凝集素和大豆凝集素的反应性增加。仅在取自分化程度较低乳腺的人乳腺上皮细胞(A组和B组)中观察到这种反应,而取自小叶发育良好乳腺的人乳腺上皮细胞(C组)未表现出这些变化。在处理后的细胞中未检测到核型异常,并且将其注射到裸鼠体内时未能诱导肿瘤形成。得出的结论是,乳腺发育与年龄无关,但受供体的生育和临床病史的强烈影响。(摘要截断于400字)