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鉴定3T3-L1前脂肪细胞分泌的对人MCF-7乳腺癌细胞系具有抑制作用的一种蛋白质因子。

Identification of a protein factor secreted by 3T3-L1 preadipocytes inhibitory for the human MCF-7 breast cancer cell line.

作者信息

Johnston P G, Rondinone C M, Voeller D, Allegra C J

机构信息

National Cancer Institute-Navy Medical Oncology Branch, NIH, Bethesda 20889.

出版信息

Cancer Res. 1992 Dec 15;52(24):6860-5.

PMID:1458474
Abstract

The 3T3-L1 cell line is a preadipocyte cell line derived from the Swiss 3T3 mouse fibroblast cell line. We have compared the effect of 3T3-L1 conditioned medium (3T3-L1 CM) and Swiss 3T3 conditioned medium (3T3 CM) on the growth of normal mouse mammary cells (NMMG) and the human MCF-7 breast carcinoma cell line. 3T3 CM increased the growth of both NMMG and MCF-7 cells by 19 +/- 2% (SD) and 24 +/- 3%, respectively, and increased thymidine incorporation by 74 +/- 4% and 104 +/- 8%, respectively. Conditioned medium from 3T3-L1 cells stimulated the growth of NMMG cells by 64 +/- 2%; in contrast, 3T3-L1 CM inhibited the growth of MCF-7 cells by 36 +/- 1%. In parallel with these growth studies, thymidine incorporation increased by 20 +/- 4% in NMMG cells and decreased by 72 +/- 5% in the MCF-7 cells. Moreover, a similar effect was also noted in NCI H630 colon cancer cells, where 3T3-L1 CM produced a 58 +/- 4% decrease in growth and a 82 +/- 6% decrease in thymidine incorporation. Heating the 3T3-L1 CM at 100 degrees C for 30 min destroyed all inhibitory activity. Several known inhibitory growth factors (fibroblast growth factor, 20 ng/ml; interleukin 6, 1000 units/ml; tumor necrosis factor alpha, 15 ng/ml; transforming growth factor beta, 1 ng/ml) were tested for activity in the MCF-7 cells. Tumor necrosis factor alpha and transforming growth factor beta produced a 97% and 67% inhibition of thymidine uptake, respectively, whereas interleukin 6 and fibroblast growth factor had no effect. Neither transforming growth factor beta nor tumor necrosis factor alpha activity was detectable in 3T3-L1 CM using an enzyme-linked immunosorbent assay. High-performance liquid chromatography fractionation of the 3T3-L1 CM revealed that the inhibitory activity eluted at a molecular weight of 67,000; moreover, silver staining of these eluates on a denaturing polyacrylamide gel revealed that M(r) 69,000 peptide was the predominant protein band in the inhibitory fractions. Thus 3T3-L1 CM stimulates the growth of normal breast epithelial cells and inhibits the growth of MCF-7 breast cancer cells. This inhibitory activity appears to be due to a protein secreted by 3T3-L1 preadipocytes.

摘要

3T3-L1细胞系是一种从前脂肪细胞系,源自瑞士3T3小鼠成纤维细胞系。我们比较了3T3-L1条件培养基(3T3-L1 CM)和瑞士3T3条件培养基(3T3 CM)对正常小鼠乳腺细胞(NMMG)和人MCF-7乳腺癌细胞系生长的影响。3T3 CM使NMMG和MCF-7细胞的生长分别增加了19±2%(标准差)和24±3%,并使胸苷掺入分别增加了74±4%和104±8%。3T3-L1细胞的条件培养基使NMMG细胞的生长增加了64±2%;相比之下,3T3-L1 CM使MCF-7细胞的生长受到36±1%的抑制。与这些生长研究并行的是,NMMG细胞中的胸苷掺入增加了20±4%,而MCF-7细胞中的胸苷掺入减少了72±5%。此外,在NCI H630结肠癌细胞中也观察到了类似的效应,其中3T3-L1 CM使生长减少了58±4%,胸苷掺入减少了82±6%。将3T3-L1 CM在100℃加热30分钟可破坏所有抑制活性。测试了几种已知的抑制生长因子(成纤维细胞生长因子,20 ng/ml;白细胞介素6,1000单位/ml;肿瘤坏死因子α,15 ng/ml;转化生长因子β,1 ng/ml)在MCF-7细胞中的活性。肿瘤坏死因子α和转化生长因子β分别使胸苷摄取受到97%和67%的抑制,而白细胞介素6和成纤维细胞生长因子则没有作用。使用酶联免疫吸附测定法在3T3-L1 CM中未检测到转化生长因子β或肿瘤坏死因子α的活性。对3T3-L1 CM进行高效液相色谱分离显示,抑制活性在分子量为67,000时洗脱;此外,在变性聚丙烯酰胺凝胶上对这些洗脱物进行银染显示,M(r) 69,000肽是抑制组分中的主要蛋白条带。因此,3T3-L1 CM刺激正常乳腺上皮细胞的生长并抑制MCF-7乳腺癌细胞的生长。这种抑制活性似乎是由于3T3-L1前脂肪细胞分泌的一种蛋白质所致。

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