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转化生长因子-β信号转导的调控作为治疗结直肠癌的一种治疗方法。

Regulation of transforming growth factor-β signaling as a therapeutic approach to treating colorectal cancer.

机构信息

Department of Medical and Clinical Biochemistry, Faculty of Medicine, Pavol Jozef Safarik University in Kosice, Kosice 04011, Slovakia.

First Department of Surgery, Medical Faculty of Safarik University, Kosice 04011, Kosicky kraj, Slovakia.

出版信息

World J Gastroenterol. 2022 Sep 7;28(33):4744-4761. doi: 10.3748/wjg.v28.i33.4744.


DOI:10.3748/wjg.v28.i33.4744
PMID:36156927
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9476856/
Abstract

According to data from 2020, Slovakia has long been among the top five countries with the highest incidence rate of colorectal cancer (CRC) worldwide, and the rate is continuing to rise every year. In approximately 80% of CRC cases, allelic loss (loss of heterozygosity, LOH) occurs in the long arm of chromosome 18q. The most important genes that can be silenced by 18q LOH or mutations are small mothers against decapentaplegic homolog (SMAD) 2 and SMAD4, which are intracellular mediators of transforming growth factor (TGF)-β superfamily signals. TGF-β plays an important role in the pro-oncogenic processes, including such properties as invasion, epithelial-mesenchymal transition (commonly known as EMT), promotion of angiogenesis, and immunomodulatory effects. Several recent studies have reported that activation of TGF-β signaling is related to drug resistance in CRC. Because the mechanisms of drug resistance are different between patients in different stages of CRC, personalized treatment is more effective. Therefore, knowledge of the activation and inhibition of factors that affect the TGF-β signaling pathway is very important.

摘要

根据 2020 年的数据,斯洛伐克长期以来一直是全球结直肠癌(CRC)发病率最高的五个国家之一,且发病率每年都在持续上升。在大约 80%的 CRC 病例中,18 号染色体长臂会发生等位基因缺失(杂合性丢失,LOH)。18q LOH 或突变可使小 mothers against decapentaplegic 同源物(SMAD)2 和 SMAD4 这两个最重要的基因失活,它们是转化生长因子(TGF)-β 超家族信号的细胞内介质。TGF-β 在致癌过程中发挥着重要作用,包括侵袭、上皮-间充质转化(通常称为 EMT)、促进血管生成和免疫调节作用等特性。最近的几项研究报告称,TGF-β 信号的激活与 CRC 中的耐药性有关。由于 CRC 不同阶段患者的耐药机制不同,个性化治疗更有效。因此,了解影响 TGF-β 信号通路的因素的激活和抑制非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/617012d5f238/WJG-28-4744-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/513ef788ce66/WJG-28-4744-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/f1f1ccf729ea/WJG-28-4744-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/60b9d793d9e1/WJG-28-4744-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/e3f79bd0d90c/WJG-28-4744-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/617012d5f238/WJG-28-4744-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/513ef788ce66/WJG-28-4744-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/f1f1ccf729ea/WJG-28-4744-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/60b9d793d9e1/WJG-28-4744-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/e3f79bd0d90c/WJG-28-4744-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9716/9476856/617012d5f238/WJG-28-4744-g005.jpg

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引用本文的文献

[1]
Integrating next-generation sequencing and artificial intelligence for the identification and validation of pathogenic variants in colorectal cancer.

Front Oncol. 2025-5-19

[2]
Expression of individual members of the TGF-β/SMAD signalling pathway in the progression and survival of patients with colorectal carcinoma.

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[3]
Investigating the impact of SMAD2 and SMAD4 downregulation in colorectal cancer and their correlation with immune markers, prognosis, and drug resistance and sensitivity.

Mol Biol Rep. 2024-7-22

[4]
Deciphering treatment resistance in metastatic colorectal cancer: roles of drug transports, EGFR mutations, and HGF/c-MET signaling.

Front Pharmacol. 2024-1-10

[5]
Genetic Alterations of NF-κB and Its Regulators: A Rich Platform to Advance Colorectal Cancer Diagnosis and Treatment.

Int J Mol Sci. 2023-12-21

[6]
Targeting the TGF-β Signaling Axis in Metastatic Colorectal Cancer: Where Do We Stand?

Int J Mol Sci. 2023-12-4

[7]
Stage-Dependent Levels of Brain-Derived Neurotrophic Factor and Matrix Metalloproteinase 9 in the Prognosis of Colorectal Cancer.

Biomedicines. 2023-6-26

[8]
TGFβ and the Tumor Microenvironment in Colorectal Cancer.

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[9]
Transforming Growth Factor-β1 in Cancer Immunology: Opportunities for Immunotherapy.

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[10]
Relationship between Epithelial-to-Mesenchymal Transition and Tumor-Associated Macrophages in Colorectal Liver Metastases.

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本文引用的文献

[1]
Development of DNA aptamers specific for small therapeutic peptides using a modified SELEX method.

J Microbiol. 2022-7

[2]
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Cancer Cell Int. 2022-6-8

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Silencing LncRNA CASC9 inhibits proliferation and invasion of colorectal cancer cells by MiR-542-3p/ILK.

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Int J Oncol. 2022-6

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SMAD4 mutations identified in Iranian patients with colorectal cancer and polyp.

Gastroenterol Hepatol Bed Bench. 2021

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circPTEN1, a circular RNA generated from PTEN, suppresses cancer progression through inhibition of TGF-β/Smad signaling.

Mol Cancer. 2022-2-8

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Association of SMAD7 genetic markers and haplotypes with colorectal cancer risk.

BMC Med Genomics. 2022-1-11

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