SOX7 Target Genes and Their Contribution to Its Tumor Suppressive Function.

SOX7 Target Genes and Their Contribution to Its Tumor Suppressive Function.
复制标题

SOX7靶基因及其对肿瘤抑制功能的贡献

DOI:
10.3390/ijms19051451
复制
发表时间:
2018-05-14
影响因子:
5.6
通讯作者:
Sui G
Sui G
中科院分区:
生物学2区
文献类型:
--
作者:
Zhang Y;Stovall DB;Wan M;Zhang Q;Chou JW;Li D;Sui G

文献摘要

参考文献

相似文献

SOX 7是一种转录因子,并作为一种肿瘤抑制因子,但其在癌症中的靶基因很少探索。我们使用微阵列芯片揭示了SOX7介导的乳腺癌细胞基因表达谱,并发现了多种改变的信号通路。当结合分析来自759名乳腺癌患者的基因阵列数据集的微阵列数据时,我们确定了4个基因作为SOX 7的潜在靶点,并通过定量PCR和染色质免疫沉淀试验对其进行了验证。在这四个基因中,我们确定了SOX 7激活的SPRY1和SLIT 2,以及SOX 7抑制的TRIB 3和MTHFD 2都可以不同地促进SOX 7介导的肿瘤抑制。总的来说,我们确定了由SOX 7介导的多种癌症相关途径,并首次揭示了SOX 7在癌症相关背景下调节的靶基因。
SOX7 is a transcription factor and acts as a tumor suppressor, but its target genes in cancers are poorly explored. We revealed SOX7-mediated gene expression profile in breast cancer cells using microarray chips and discovered multiple altered signaling pathways. When combinatorially analyzing the microarray data with a gene array dataset from 759 breast cancer patients, we identified four genes as potential targets of SOX7 and validated them by quantitative PCR and chromatin immunoprecipitation assays. Among these four genes, we determined that SOX7-activated SPRY1 and SLIT2, and SOX7-repressed TRIB3 and MTHFD2 could all differentially contribute to SOX7-mediated tumor suppression. Overall, we identified multiple cancer-related pathways mediated by SOX7 and for the first time revealed SOX7-regulated target genes in a cancer-relevant context.
DOI: 10.1007/s11010-009-0359-z
发表时间: 2010-05
影响因子: 4.3
作者:
Lee, Sangjin;Nguyen, Tri M. Bui;Kovalenko, Dmitry;Adhikari, Neeta;Grindle, Suzanne;Polster, Sean P.;Friesel, Robert;Ramakrishnan, Sundaram;Hall, Jennifer L.
通讯作者: Hall, Jennifer L.
miR-9通过靶向SOX7参与TGF-β1诱导的肺癌细胞侵袭和粘附。
DOI: 10.1111/jcmm.13120
发表时间: 2017-09
影响因子: 5.3
作者:
Han L;Wang W;Ding W;Zhang L
通讯作者: Zhang L
DOI: 10.1002/dvdy.22046
发表时间: 2010-01
影响因子: 2.5
作者:
Kormish, Jay D.;Sinner, Debora;Zorn, Aaron M.
通讯作者: Zorn, Aaron M.
DOI: 10.26355/eurrev_201712_14006
发表时间: 2017-12-01
影响因子: 3.3
作者:
Bai, Q. -L.;Hu, C. -W.;Yin, G. -F.
通讯作者: Yin, G. -F.
DOI: 10.1073/pnas.1214014110
发表时间: 2013-01-29
影响因子: 11.1
作者:
Izrailit, Julia;Berman, Hal K.;Reedijk, Michael
通讯作者: Reedijk, Michael