Guzman R C, Osborn R C, Bartley J C, Nandi S
Cancer Research Laboratory, University of California, Berkeley 94720.
Cancer Lett. 1988 Jun 15;40(2):123-32. doi: 10.1016/0304-3835(88)90002-x.
Mammary epithelial cells from 3-4-month-old BALB/c virgin mice were cultured inside collagen gels in the following serum-free media: Dulbecco's Modified Eagle's Medium/Ham's F-12 (1:1) supplemented with (A) insulin, bovine serum albumin, epidermal growth factor; (B) insulin, bovine serum albumin, progesterone, prolactin; (C) insulin, bovine serum albumin, progesterone, prolactin, linoleic acid. Cell number increased with all media used. At day 7 of culture, [3H]dimethylbenz[a]anthracene (DMBA) was added to the cultures and its metabolism to water soluble and organic soluble compounds was determined. Mouse mammary epithelial cells were able to metabolize [3H]DMBA to water and organosoluble metabolites. By 72 h, 77-94% of the added DMBA had been metabolized by the epithelial cells in the three media to water and organosoluble metabolites in equivalent amounts. The distribution between water soluble and organosoluble metabolites was approximately equivalent. The high pressure liquid chromatography profiles of organosoluble fractions from the media indicated that the major products appeared to be the phenols, 2-,3-, or 4-hydroxydimethylbenz[a]anthracene, the hydroxymethyl derivatives, 7-methylbenz[a]anthracene and 7-hydroxymethylbenz[a]anthracene, trans-3,4-dihydro-3,4-dihydroxydimethylbenz[a]anthracene and one or two major fractions eluting just behind the marker cis-5,6-dihydro-5,6-dihydroxydimethylbenz[a]anthracene. The major fraction eluting just ahead of the cis-5,6-dihydro-5,6-dihydroxydimethylbenz[a]anthracene was most likely trans-8,9-dihydro 8,9-dihydroxydimethylbenz[a]anthracene. The profiles were similar for the cells cultured in all three serum-free media. The results demonstrate that mouse mammary epithelial cells cultured inside collagen gels with serum-free media can metabolize DMBA to putative carcinogenic forms.
取自3 - 4月龄BALB/c处女小鼠的乳腺上皮细胞,在以下无血清培养基中于胶原凝胶内进行培养:杜尔贝科改良伊格尔培养基/哈姆F - 12培养基(1:1),添加(A)胰岛素、牛血清白蛋白、表皮生长因子;(B)胰岛素、牛血清白蛋白、孕酮、催乳素;(C)胰岛素、牛血清白蛋白、孕酮、催乳素、亚油酸。使用的所有培养基均使细胞数量增加。培养第7天时,向培养物中加入[3H]二甲基苯并[a]蒽(DMBA),并测定其代谢为水溶性和有机溶性化合物的情况。小鼠乳腺上皮细胞能够将[3H]DMBA代谢为水溶性和有机溶性代谢物。到72小时时,三种培养基中的上皮细胞已将77 - 94%添加的DMBA代谢为等量的水溶性和有机溶性代谢物。水溶性和有机溶性代谢物之间的分布大致相等。培养基中有机溶性部分的高压液相色谱图谱表明,主要产物似乎是酚类、2 -、3 - 或4 - 羟基二甲基苯并[a]蒽、羟甲基衍生物、7 - 甲基苯并[a]蒽和7 - 羟甲基苯并[a]蒽、反式 - 3,4 - 二氢 - 3,4 - 二羟基二甲基苯并[a]蒽以及在标记物顺式 - 5,6 - 二氢 - 5,6 - 二羟基二甲基苯并[a]蒽之后洗脱的一两个主要组分。恰好在顺式 - 5,6 - 二氢 - 5,6 - 二羟基二甲基苯并[a]蒽之前洗脱的主要组分很可能是反式 - 8,9 - 二氢 - 8,9 - 二羟基二甲基苯并[a]蒽。在所有三种无血清培养基中培养的细胞的图谱相似。结果表明,在胶原凝胶内用无血清培养基培养的小鼠乳腺上皮细胞可将DMBA代谢为推定的致癌形式。