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首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Application of open-access databases to determine functional connectivity between resveratrol-binding protein QR2 and colorectal carcinoma
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Application of open-access databases to determine functional connectivity between resveratrol-binding protein QR2 and colorectal carcinoma

机译:开放式访问数据库的应用来确定白藜芦醇结合蛋白QR2与结直肠癌之间的功能连通性

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摘要

Colorectal cancer (CRC) is a major cause of cancerassociated deaths worldwide. Recently, oral administration of resveratrol (trans-3,5,4'-trihydroxystilbene) has been reported to significantly reduce tumor proliferation in colorectal cancer patients, however, with little specific information on functional connections. The pathogenesis and development of colorectal cancer is a multistep process that can be categorized using three phenotypic pathways, respectively, chromosome instability (CIN), microsatellite instability (MSI), and CpG island methylator (CIMP). Targets of resveratrol, including a high-affinity binding protein, quinone reductase 2 (QR2), have been identified with little information on disease association. We hypothesize that the relationship between resveratrol and different CRC etiologies might be gleaned using publicly available databases. Aweb-based microarray gene expression data-mining platform, Oncomine, was selected and used to determine whether QR2 may serve as a mechanistic and functional biotarget within the various CRC etiologies. We found that QR2 messenger RNA (mRNA) is overexpressed in CRC characterized by CIN, particularly in cells showing a positive KRAS (Kirsten rat sarcoma viral oncogene homolog) mutation, as well as by the MSI but not the CIMP phenotype. Mining of Oncomine revealed an excellent correlation between QR2 mRNA expression and certain CRC etiologies. Two resveratrol-associated genes, adenomatous polyposis coli (APC) and TP53, found in CRC were further mined, using cBio portal and Colorectal Cancer Atlas which predicted a mechanistic link to exist between resveratrol -> QR2/TP53 -> CIN. Multiple web-based data mining can provide valuable insights which may lead to hypotheses serving to guide clinical trials and design of therapies for enhanced disease prognosis and patient survival. This approach resembles a BioGPS, a capability for mining web-based databases that can elucidate the potential links between compounds to provide correlations of these interactions with specific diseases.
机译:结肠直肠癌(CRC)是全球癌症死亡的主要原因。最近,据报道,白藜芦醇(Trans-3,5,4'-Trihydroxystilbene)的口服给药,以显着降低结肠直肠癌患者的肿瘤增殖,几乎没有关于功能联系的具体信息。结直肠癌的发病机制和发育是多步骤过程,可以分别使用三种表型途径分类,染色体不稳定性(CIN),微卫星不稳定性(MSI)和CPG岛甲基甲基(CIMP)。已经鉴定了白藜芦醇的靶标,包括高亲和力结合蛋白,醌还原酶2(QR2),几乎没有关于疾病协会的信息。我们假设使用公开的数据库,可能会收集白藜芦醇和不同CRC病因之间的关系。基于AWEB的微阵列基因表达数据挖掘平台,oncomsine被选择并用于确定QR2是否可以作为各种CRC病因内的机械和功能生物术。我们发现QR2信使RNA(mRNA)在CRC中过表达,其特征在于CIN,特别是在显示阳性KRAS(Kirsten大鼠Sarcoma病毒癌基因同源物)突变的细胞中,以及MSI但不是CIMP表型。 oncomine的开采揭示了QR2 mRNA表达与某些CRC病因之间的优异相关性。进一步开采了两种白藜芦醇相关基因,在CRC中发现的腺瘤性息肉(APC)和TP53,使用CBIO门尔和结直肠癌地图集,预测白藜芦醇 - > QR2 / TP53 - > CIN之间存在的机械链路。基于多个基于Web的数据挖掘可以提供有价值的见解,这可能导致假设用于指导临床试验和疗法设计,以提高疾病预后和患者存活。该方法类似于BioGPS,一种能够挖掘基于网的数据库,可以阐明化合物之间的潜在环节,以提供这些与特定疾病的这些相互作用的相关性。

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