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RNA结合基序蛋白22通过c-Myc途径诱导结肠癌细胞凋亡。

RNA-Binding Motif Protein 22 Induces Apoptosis via c-Myc Pathway in Colon Cancer Cells.

作者信息

Park Ye-Rin, Park So-Mi, Kim Nanyeong, Jung Jihoon, Kim Seokwoo, Kim Kwan-Il, Jang Hyeung-Jin

机构信息

College of Korean Medicine, Kyung Hee University, 26, Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Republic of Korea.

Department of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.

出版信息

Molecules. 2025 Mar 9;30(6):1227. doi: 10.3390/molecules30061227.

DOI:10.3390/molecules30061227
PMID:40142004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11945962/
Abstract

RNA-binding motif 22 (RBM22) is an RNA-binding protein involved in gene regulation, with the capacity to bind DNA and function as a transcription factor for various target genes. Recent studies demonstrated that RBM22 depletion affects cell viability and proliferation of glioblastoma and breast cancer cells. However, the role of RBM22 in colon cancer and the molecular mechanisms underlying its tumor-suppressive function remain largely unclear. In this study, we demonstrate that RBM22 induces apoptosis and suppresses colon cancer cell viability and proliferation by modulating c-Myc expression. Furthermore, RBM22 knockdown reduces c-Myc stability. Therefore, our findings suggest that RBM22 depletion regulates cancer cell proliferation and induces apoptosis via the c-Myc pathway.

摘要

RNA结合基序22(RBM22)是一种参与基因调控的RNA结合蛋白,具有结合DNA的能力,并作为各种靶基因的转录因子发挥作用。最近的研究表明,RBM22缺失会影响胶质母细胞瘤和乳腺癌细胞的细胞活力和增殖。然而,RBM22在结肠癌中的作用及其肿瘤抑制功能的分子机制仍不清楚。在本研究中,我们证明RBM22通过调节c-Myc表达诱导细胞凋亡并抑制结肠癌细胞的活力和增殖。此外,RBM22敲低降低了c-Myc的稳定性。因此,我们的研究结果表明,RBM22缺失通过c-Myc途径调节癌细胞增殖并诱导细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/5453295ab350/molecules-30-01227-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/4a3137f41ae7/molecules-30-01227-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/2bc121bc4c62/molecules-30-01227-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/bed3f7202115/molecules-30-01227-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/0427cfe0beef/molecules-30-01227-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/5453295ab350/molecules-30-01227-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/4a3137f41ae7/molecules-30-01227-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/2bc121bc4c62/molecules-30-01227-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/bed3f7202115/molecules-30-01227-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/0427cfe0beef/molecules-30-01227-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d408/11945962/5453295ab350/molecules-30-01227-g005.jpg

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本文引用的文献

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Int J Mol Sci. 2023 Dec 18;24(24):17589. doi: 10.3390/ijms242417589.
2
Ophiopogonin D increase apoptosis by activating p53 ribosomal protein L5 and L11 and inhibiting the expression of c-Myc CNOT2.麦冬皂苷D通过激活p53、核糖体蛋白L5和L11并抑制c-Myc、CNOT2的表达来增加细胞凋亡。
Front Pharmacol. 2022 Dec 9;13:974468. doi: 10.3389/fphar.2022.974468. eCollection 2022.
3
Methods of PARP-1 Determination and its Importance in Living Organisms.
PARP-1 的测定方法及其在生物活体中的重要性。
Protein Pept Lett. 2022;29(6):496-504. doi: 10.2174/0929866529666220405160715.
4
RBM22, a Key Player of Pre-mRNA Splicing and Gene Expression Regulation, Is Altered in Cancer.RBM22是前体mRNA剪接和基因表达调控的关键因子,在癌症中发生改变。
Cancers (Basel). 2022 Jan 27;14(3):643. doi: 10.3390/cancers14030643.
5
Cancer statistics in China and United States, 2022: profiles, trends, and determinants.中国和美国 2022 年癌症统计数据:概况、趋势和决定因素。
Chin Med J (Engl). 2022 Feb 9;135(5):584-590. doi: 10.1097/CM9.0000000000002108.
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Inhibition of CNOT2 Induces Apoptosis via MID1IP1 in Colorectal Cancer Cells by Activating p53.抑制 CNOT2 通过激活 p53 诱导结直肠癌细胞中的 MID1IP1 诱导细胞凋亡。
Biomolecules. 2021 Oct 10;11(10):1492. doi: 10.3390/biom11101492.
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Splicing machinery dysregulation drives glioblastoma development/aggressiveness: oncogenic role of SRSF3.剪接体调控失调驱动胶质母细胞瘤发生/侵袭:SRSF3 的致癌作用。
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