首页> 外文期刊>The Journal of Steroid Biochemistry and Molecular Biology >Sex hormone binding globulin mRNA in human breast cancer: detection in cell lines and tumor samples.
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Sex hormone binding globulin mRNA in human breast cancer: detection in cell lines and tumor samples.

机译:人乳腺癌中性激素结合球蛋白的mRNA:在细胞系和肿瘤样品中的检测。

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Sex hormone binding globulin (SHBG) is a high affinity binding protein for estrogens and androgens. SHBG has been found in breast tissue and cell lines through immunostaining. The goal of this series of experiments was to determine whether mRNA for SHBG is expressed in breast cancer cell lines and tumor tissue. Reverse transcriptase-polymerase chain reaction (RT-PCR) was used to detect SHBG and beta-2 microglobulin (control for tissue extractions). Three breast cancer cell lines, ZR-75-1, MCF-7, and MDA-MB-231 and 56 breast tissue samples were collected and analysed for SHBG mRNA expression. mRNA was successfully extracted from 30 of these breast tissue samples. SHBG mRNA was detected in ZR-75-1, MCF-7 and MDA-MB-231 cells, and in 11 of the breast tissue samples. Two PCR products were routinely amplified from the breast cancer cell line RNA, one at approximately 500 bp and another at approximately 300 bp. The DNA sequence of the 300 bp PCR produce was consistent with alternate splicing of the SHBG mRNA, where exon 7 is deleted, and is accompanied by a point deletion at the beginning of exon 8. SHBG protein production from the three breast cancer cell lines was detected by immunoprecipitation using an affinity purified SHBG antibody. SHBG mRNA was found in 11 of 30 samples of breast tissue. Some samples expressed only the 500 bp or the 300 bp PCR product, whereas others expressed both PCR products. The presence of SHBG mRNA in these samples was not associated with either the presence or absence of steroid receptors. SHBG mRNA is thus expressed in breast cancer cell lines, and in some breast tissue samples.
机译:性激素结合球蛋白(SHBG)是雌激素和雄激素的高亲和力结合蛋白。通过免疫染色在乳腺组织和细胞系中发现了SHBG。这一系列实验的目的是确定SHBG的mRNA是否在乳腺癌细胞系和肿瘤组织中表达。逆转录聚合酶链反应(RT-PCR)用于检测SHBG和β-2微球蛋白(用于组织提取的对照)。收集了三个乳腺癌细胞系ZR-75-1,MCF-7和MDA-MB-231和56个乳腺癌组织样品,并分析了SHBG mRNA的表达。从30个这些乳腺组织样本中成功提取了mRNA。在ZR-75-1,MCF-7和MDA-MB-231细胞以及11个乳腺组织样品中检测到SHBG mRNA。从乳腺癌细胞系RNA常规扩增两种PCR产物,一种以约500bp,另一种以约300bp。 300 bp PCR产物的DNA序列与SHBG mRNA的可变剪接一致,其中第7外显子被删除,并且在第8外显子的开始处有一个点缺失。使用亲和纯化的SHBG抗体通过免疫沉淀法检测。在30个乳腺组织样本中有11个发现了SHBG mRNA。一些样品仅表达500 bp或300 bp PCR产物,而其他样品则表达两种PCR产物。这些样品中SHBG mRNA的存在与类固醇受体的存在与否无关。因此,SHBG mRNA在乳腺癌细胞系和某些乳腺癌组织样品中表达。

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