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他莫昔芬对雌激素依赖性MCF-7乳腺癌细胞中纤连蛋白表达的调节作用。

The regulatory effect of tamoxifen on fibronectin expression in estrogen-dependent MCF-7 breast carcinoma cells.

作者信息

Horii Yoshio, Takei Hiroyuki, Koibuchi Yukio, Horiguchi Jun, Maemura Michio, Iino Yuichi, Morishita Yasuo

机构信息

Department of Thoracic and Visceral Organ Surgery, Gunma University Graduate School of Medicine, Maebashi, Gunma 371-8511, Japan.

出版信息

Oncol Rep. 2006 May;15(5):1191-5.

Abstract

We investigated the regulatory effect of tamoxifen (TAM) on fibronectin (FN) expression in estrogen-dependent MCF-7 breast carcinoma cells both in vitro and in vivo. in vitro, MCF-7 cells were cultured with 17beta-estradiol (E2) and/or TAM. In the animal experiment in vivo, MCF-7 tumors were grown in ovariectomized athymic mice by implanting a sustained release E2 pellet. The E2 pellets were removed after 3 weeks of E2 treatment. Animals were then divided into four groups: 1) an E2 (0.72 mg/pellet) pellet [E2(+)]; 2) an E2 and a TAM (5 mg/pellet) pellet [E2(+)TAM]; 3) no treatment [E2(-)] and 4) a TAM pellet [E2(-)TAM]. Following each treatment for 4 weeks, all animals were sacrificed and tumors were removed. Specimens, cells (in vitro) or tumors (in vivo), were homogenized and assayed for FN by Western blots. In the in vitro experiment, FN expression in MCF-7 cells decreased by incubating with 10(-9) M E2 and increased with 10(-6) M TAM. The effect of TAM increasing FN expression was inhibited by incubation accompanied with 10(-9) M E2 or 1 microg/ml transforming growth factor-beta (TGF-beta) neutralizing antibody. In the in vivo animal experiment FN expression in the tumors of E2(+) mice was lower than that of E2(-) mice. However, TAM increased FN expression in the tumors regardless of E2 pellet. These results suggest that TAM increases FN expression of MCF-7 breast carcinoma cells and that these regulatory effects of TAM on FN expression are partly mediated by TAM-induced TGF-beta.

摘要

我们在体外和体内研究了他莫昔芬(TAM)对雌激素依赖性MCF-7乳腺癌细胞中纤连蛋白(FN)表达的调节作用。在体外,MCF-7细胞用17β-雌二醇(E2)和/或TAM培养。在体内动物实验中,通过植入缓释E2丸粒在去卵巢的无胸腺小鼠中培养MCF-7肿瘤。E2处理3周后取出E2丸粒。然后将动物分为四组:1)E2(0.72mg/丸粒)丸粒组[E2(+)];2)E2和TAM(5mg/丸粒)丸粒组[E2(+)TAM];3)不处理组[E2(-)];4)TAM丸粒组[E2(-)TAM]。每种处理4周后,处死所有动物并取出肿瘤。对标本、细胞(体外)或肿瘤(体内)进行匀浆,并通过蛋白质免疫印迹法检测FN。在体外实验中,与10(-9)M E2孵育可使MCF-7细胞中FN表达降低,而与10(-6)M TAM孵育则使其增加。与10(-9)M E2或1μg/ml转化生长因子-β(TGF-β)中和抗体共同孵育可抑制TAM增加FN表达的作用。在体内动物实验中,E2(+)小鼠肿瘤中的FN表达低于E2(-)小鼠。然而,无论有无E2丸粒,TAM均可增加肿瘤中FN的表达。这些结果表明,TAM可增加MCF-7乳腺癌细胞中FN的表达,且TAM对FN表达的这些调节作用部分是由TAM诱导的TGF-β介导的。

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