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AGR2-mediated lung adenocarcinoma metastasis novel mechanism network through repression with interferon coupling cytoskeleton to steroid metabolism-dependent humoral immune response

机译:AGR2介导的肺腺癌转移新机制网络通过抑制与干扰素偶联的细胞骨架与类固醇代谢依赖的体液免疫反应

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摘要

7 anterior gradient homolog 2 (AGR2)-inhibited different molecular mutual positive correlation network was constructed in lung adenocarcinoma compared with human normal adjacent tissues by 17 overlapping molecules of 358 GRNInfer and 19 Pearson (AGR2 CC. ≤. -0.25). Based on GO, KEGG, GenMAPP, BioCarta and disease databases, we determined AGR2-mediated lung adenocarcinoma metastasis through repression with cytoskeleton of MAST1; steroid metabolism of SOAT2; humoral immune response of POU2AF1; interferon alpha-inducible of IFI6; immunoglobulin of IGKC_3, CTA_246H3.1. Thus we proposed AGR2-mediated lung adenocarcinoma metastasis novel mechanism network through repression with interferon coupling cytoskeleton to steroid metabolism-dependent humoral immune response.
机译:与人正常相邻组织相比,在肺腺癌中,通过17个重叠分子358 GRNInfer和19 Pearson(AGR2 CC。≤.-0.25),构建了7个前梯度同源物2(AGR2)抑制的不同分子相互正相关网络。基于GO,KEGG,GenMAPP,BioCarta和疾病数据库,我们通过抑制MAST1的细胞骨架来确定AGR2介导的肺腺癌转移。 SOAT2的类固醇代谢; POU2AF1的体液免疫反应; IFI6的α干扰素诱导型; IGKC_3,CTA_246H3.1的免疫球蛋白。因此,我们提出了通过抑制干扰素将细胞骨架偶联至类固醇代谢依赖的体液免疫反应来抑制AGR2介导的肺腺癌转移的新机制网络。

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