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LRP11、FUBP1 和 TET1 在宫颈癌中的表达及临床价值。

The expression and clinical value of LRP11, FUBP1 and TET1 in cervical cancer.

机构信息

Inspection Center, the First Hospital of Hebei Medical University, Shijiazhuang, Hebei050031, China.

Department of Blood Transfusion, the First Hospital of Hebei Medical University, Shijiazhuang, Hebei050031, China.

出版信息

Cell Mol Biol (Noisy-le-grand). 2023 Jul 31;69(7):80-84. doi: 10.14715/cmb/2023.69.7.13.

DOI:10.14715/cmb/2023.69.7.13
PMID:37715422
Abstract

Cervical cancer is the second leading cause of cancer death among women worldwide. Identification of effective genes along with biological markers as targeting agents is very necessary for the diagnosis and treatment of this disease. Bioinformatics techniques along with genetic and molecular investigations have provided the possibility of studying different levels of information such as the genome, transcriptome, proteome, and metabolize with high depth and accuracy. The collection of these data provides comprehensive and valuable information about the investigated phenotypes, including complex diseases such as cancer. In this study, we examined three genes LRP11, FUBP1, and TET1 related to cervical cancer. The results of this study showed that the level of expression of these genes is high in lymph nodes and the thyroid and is less in the pancreas and liver. Also, the expression level of the FUBP1 gene is higher than that of LRP11, and the expression level of the LRP11 gene is higher than that of TET1. Regarding the structure and proteomics of the studied genes, it can be seen that due to the presence of more domains in the LRP11 and FUBP1 genes, these genes probably independently participate in various functions and have a wider range of activity than the TET1 gene. Also, the analysis of the stability of the examined genes showed that the stability of the FUBP1 gene is relatively higher than that of the TET1 gene, and this gene is also more stable than the LRP11 gene. Considering that these genes are effective key genes for the early detection of cervical cancer, it is hoped that they will be used as markers in the diagnosis and treatment of cervical cancer.

摘要

宫颈癌是全球女性癌症死亡的第二大主要原因。鉴定有效的基因和生物标志物作为靶向治疗剂对于该疾病的诊断和治疗非常必要。生物信息学技术以及遗传和分子研究为研究不同层次的信息提供了可能性,例如基因组、转录组、蛋白质组和代谢组,具有高深度和准确性。这些数据的收集提供了有关所研究表型的全面和有价值的信息,包括癌症等复杂疾病。在这项研究中,我们研究了与宫颈癌相关的三个基因 LRP11、FUBP1 和 TET1。研究结果表明,这些基因在淋巴结和甲状腺中的表达水平较高,在胰腺和肝脏中的表达水平较低。此外,FUBP1 基因的表达水平高于 LRP11,而 LRP11 基因的表达水平高于 TET1。关于研究基因的结构和蛋白质组学,可以看出由于 LRP11 和 FUBP1 基因中存在更多的结构域,这些基因可能独立参与各种功能,并且比 TET1 基因具有更广泛的活性范围。此外,对所研究基因稳定性的分析表明,FUBP1 基因的稳定性相对高于 TET1 基因,并且该基因也比 LRP11 基因更稳定。鉴于这些基因是早期检测宫颈癌的有效关键基因,希望它们能作为宫颈癌诊断和治疗的标志物。

相似文献

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The expression and clinical value of LRP11, FUBP1 and TET1 in cervical cancer.LRP11、FUBP1 和 TET1 在宫颈癌中的表达及临床价值。
Cell Mol Biol (Noisy-le-grand). 2023 Jul 31;69(7):80-84. doi: 10.14715/cmb/2023.69.7.13.
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An integrative pan-cancer analysis illustrating the key role of LRP11 in cervical cancer.一项综合的泛癌症分析表明 LRP11 在宫颈癌中的关键作用。
Medicine (Baltimore). 2023 Mar 17;102(11):e33201. doi: 10.1097/MD.0000000000033201.
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High nuclear expression of DNMT1 in correlation with inactivation of TET1 portray worst prognosis among the cervical carcinoma patients: clinical implications.高核表达的 DNMT1 与 TET1 的失活相关,预示着宫颈癌患者预后最差:临床意义。
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Overexpression of FUBP1 is associated with human cervical carcinoma development and prognosis.FUBP1 的过表达与人类宫颈癌的发生发展及预后相关。
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TNPO1-Mediated Nuclear Import of FUBP1 Contributes to Tumor Immune Evasion by Increasing NRP1 Expression in Cervical Cancer.TNPO1 介导的 FUBP1 核输入通过增加宫颈癌中 NRP1 的表达促进肿瘤免疫逃逸。
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Alterations of regulatory factors and DNA methylation pattern in thyroid cancer.甲状腺癌中调控因子和 DNA 甲基化模式的改变。
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Snail/PRMT5/NuRD complex contributes to DNA hypermethylation in cervical cancer by TET1 inhibition.蜗牛/PRMT5/NuRD 复合物通过 TET1 抑制促进宫颈癌中的 DNA 高甲基化。
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Aberrant TET1 Methylation Closely Associated with CpG Island Methylator Phenotype in Colorectal Cancer.异常的TET1甲基化与结直肠癌中的CpG岛甲基化表型密切相关。
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TET1 promotes 5hmC-dependent stemness, and inhibits a 5hmC-independent epithelial-mesenchymal transition, in cervical precancerous lesions.TET1 促进宫颈癌前病变中依赖 5hmC 的干性,并抑制非依赖 5hmC 的上皮-间充质转化。
Cancer Lett. 2019 May 28;450:53-62. doi: 10.1016/j.canlet.2019.01.033. Epub 2019 Feb 13.

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