Inhibition of KIAA0101 Expression Can Regulate Cell Proliferation and Apoptosis in Colon Cancer.

IF 2.4 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
YanWei Yu, Xingchun Xiao, Fushu Jin
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引用次数: 0

Abstract

Background: Colon cancer is a prevalent malignant tumor of digestive tract occurring in the colon. In the people with cancer, colon cancer is the third leading cause of deaths in the world. Basic research on colon cancer is of great importance to patients with the disease. Methods: In this article, the authors observed the KIAA0101 expression in different types of cancers in public database (GEPIA2), found a gene network associated with KIAA0101 in STRING database, and explored the correlation of these genes with KIAA0101 at the expression level and the immune cells associated with the expression of KIAA0101. Then the authors detected the affection of KIAA0101 to the proliferation and apoptosis of cancer cells and verified the consistency of KIAA0101 expression in 31 tumor patient tissues using the database. Results: KIAA0101 is differentially expressed in all kinds of tumor cells, and it shows high expression in colorectal cancer tissues. The authors found 10 genes related to KIAA0101, including CDC20, TOP2A, CCNB2, CCNA2, and so on, all of which show positive correlation with KIAA0101 expression. In addition, the result of this study showed that KIAA0101 expression had a positive correlation with the infiltration of Th1 and Th2 cells, with correlation coefficients of 0.371 and 0.627, respectively. KIAA0101 gene shows high expression in both HCT15 and SW480 cell lines. Inhibition of KIAA0101 expression can increase caspase 3/7 activity in both HCT15 and SW480 cell lines, inhibit the proliferation ability of the two cell lines, and inhibit Bcl-2 gene expression. KIAA0101 also has tumor-suppressing effects in mice. The expression of KIAA0101 gene also shows a significant increase in the tissues collected from 31 patients with tumor. Conclusions: Inhibition of KIAA0101 expression can regulate cell proliferation and apoptosis in colorectal cancer.

抑制KIAA0101表达可调节结肠癌细胞增殖和凋亡。
背景:结肠癌是发生在结肠的一种常见的消化道恶性肿瘤。在癌症患者中,结肠癌是世界上第三大死亡原因。结肠癌的基础研究对结肠癌患者具有重要意义。方法:本文通过在公共数据库(GEPIA2)中观察KIAA0101在不同类型癌症中的表达,在STRING数据库中发现与KIAA0101相关的基因网络,探讨这些基因与KIAA0101在表达水平上的相关性以及与KIAA0101表达相关的免疫细胞。然后检测KIAA0101对癌细胞增殖和凋亡的影响,并利用数据库验证KIAA0101在31例肿瘤患者组织中表达的一致性。结果:KIAA0101在各类肿瘤细胞中均有差异表达,且在结直肠癌组织中呈高表达。作者发现了10个与KIAA0101相关的基因,包括CDC20、TOP2A、CCNB2、CCNA2等,它们都与KIAA0101的表达呈正相关。此外,本研究结果显示KIAA0101表达与Th1、Th2细胞浸润呈正相关,相关系数分别为0.371、0.627。KIAA0101基因在HCT15和SW480细胞系中均有高表达。抑制KIAA0101表达可提高HCT15和SW480细胞系caspase 3/7活性,抑制两种细胞系的增殖能力,抑制Bcl-2基因表达。KIAA0101在小鼠中也有抑制肿瘤的作用。KIAA0101基因的表达也在31例肿瘤患者的组织中显著增加。结论:抑制KIAA0101表达可调节结直肠癌细胞增殖和凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
2.90%
发文量
87
审稿时长
3 months
期刊介绍: Cancer Biotherapy and Radiopharmaceuticals is the established peer-reviewed journal, with over 25 years of cutting-edge content on innovative therapeutic investigations to ultimately improve cancer management. It is the only journal with the specific focus of cancer biotherapy and is inclusive of monoclonal antibodies, cytokine therapy, cancer gene therapy, cell-based therapies, and other forms of immunotherapies. The Journal includes extensive reporting on advancements in radioimmunotherapy, and the use of radiopharmaceuticals and radiolabeled peptides for the development of new cancer treatments.
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