文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

肿瘤微环境在结直肠癌进展中的作用 Wnt/β-catenin 通路:提供对化疗耐药复杂机制的理解。

Tumor microenvironment involvement in colorectal cancer progression Wnt/β-catenin pathway: Providing understanding of the complex mechanisms of chemoresistance.

机构信息

Departamento de Biología, Bioquímica y Farmacia, Universidad Nacional del Sur (UNS)-INBIOSUR (CONICET-UNS), Bahía Blanca 8000, Argentina.

Departamento de Química, Universidad Nacional del Sur (UNS)-INQUISUR (CONICET-UNS), Bahía Blanca 8000, Argentina.

出版信息

World J Gastroenterol. 2022 Jul 14;28(26):3027-3046. doi: 10.3748/wjg.v28.i26.3027.


DOI:10.3748/wjg.v28.i26.3027
PMID:36051330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9331520/
Abstract

Colorectal cancer (CRC) continues to be one of the main causes of death from cancer because patients progress unfavorably due to resistance to current therapies. Dysregulation of the Wnt/β-catenin pathway plays a fundamental role in the genesis and progression of several types of cancer, including CRC. In many subtypes of CRC, hyperactivation of the β-catenin pathway is associated with mutations of the gene. However, it can also be associated with other causes. In recent years, studies of the tumor microenvironment (TME) have demonstrated its importance in the development and progression of CRC. In this tumor nest, several cell types, structures, and biomolecules interact with neoplastic cells to pave the way for the spread of the disease. Cross-communications between tumor cells and the TME are then established primarily through paracrine factors, which trigger the activation of numerous signaling pathways. Crucial advances in the field of oncology have been made in the last decade. This Minireview aims to actualize what is known about the central role of the Wnt/β-catenin pathway in CRC chemoresistance and aggressiveness, focusing on cross-communication between CRC cells and the TME. Through this analysis, our main objective was to increase the understanding of this complex disease considering a more global context. Since many treatments for advanced CRC fail due to mechanisms involving chemoresistance, the data here exposed and analyzed are of great interest for the development of novel and effective therapies.

摘要

结直肠癌(CRC)仍然是癌症死亡的主要原因之一,因为患者由于对当前疗法的耐药性而病情恶化。Wnt/β-连环蛋白途径的失调在包括 CRC 在内的几种癌症的发生和进展中起着至关重要的作用。在 CRC 的许多亚型中,β-连环蛋白途径的过度激活与基因的突变有关。然而,它也可能与其他原因有关。近年来,对肿瘤微环境(TME)的研究表明,它在 CRC 的发展和进展中具有重要作用。在这个肿瘤巢中,几种细胞类型、结构和生物分子与肿瘤细胞相互作用,为疾病的传播铺平了道路。然后,肿瘤细胞和 TME 之间建立了交叉通讯,主要是通过旁分泌因子,这些因子触发了许多信号通路的激活。在过去的十年中,肿瘤学领域取得了重要的进展。这篇综述旨在阐明 Wnt/β-连环蛋白途径在 CRC 化疗耐药性和侵袭性中的核心作用,重点关注 CRC 细胞与 TME 之间的交叉通讯。通过这种分析,我们的主要目标是从更全局的角度来增加对这种复杂疾病的理解。由于许多治疗晚期 CRC 的方法因涉及化疗耐药性的机制而失败,因此这里暴露和分析的数据对于开发新的有效治疗方法具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/9331520/f6cae2ebb6a3/WJG-28-3027-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/9331520/72873cf4aab4/WJG-28-3027-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/9331520/5c33bb4cb57b/WJG-28-3027-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/9331520/63066e6d25af/WJG-28-3027-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/9331520/f6cae2ebb6a3/WJG-28-3027-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/9331520/72873cf4aab4/WJG-28-3027-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/9331520/5c33bb4cb57b/WJG-28-3027-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/9331520/63066e6d25af/WJG-28-3027-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/9331520/f6cae2ebb6a3/WJG-28-3027-g004.jpg

相似文献

[1]
Tumor microenvironment involvement in colorectal cancer progression Wnt/β-catenin pathway: Providing understanding of the complex mechanisms of chemoresistance.

World J Gastroenterol. 2022-7-14

[2]
The lncRNA CRNDE promotes colorectal cancer cell proliferation and chemoresistance via miR-181a-5p-mediated regulation of Wnt/β-catenin signaling.

Mol Cancer. 2017-1-13

[3]
MiR-30-5p suppresses cell chemoresistance and stemness in colorectal cancer through USP22/Wnt/β-catenin signaling axis.

J Cell Mol Med. 2018-10-19

[4]
Gankyrin sustains PI3K/GSK-3β/β-catenin signal activation and promotes colorectal cancer aggressiveness and progression.

Oncotarget. 2016-12-6

[5]
Interaction of the Wnt/β-catenin and RAS-ERK pathways involving co-stabilization of both β-catenin and RAS plays important roles in the colorectal tumorigenesis.

Adv Biol Regul. 2018-5

[6]
Paired-like homeodomain transcription factor 2 strengthens chemoresistance in colorectal cancer by activating the Wnt/β-catenin axis.

Neoplasma. 2021-5

[7]
Knockdown of aquaporin-5 sensitizes colorectal cancer cells to 5-fluorouracil via inhibition of the Wnt-β-catenin signaling pathway.

Biochem Cell Biol. 2018-10

[8]
Role of Wnt/-Catenin Signaling in the Chemoresistance Modulation of Colorectal Cancer.

Biomed Res Int. 2020

[9]
LncRNA HOTAIR is a Prognostic Biomarker for the Proliferation and Chemoresistance of Colorectal Cancer via MiR-203a-3p-Mediated Wnt/ß-Catenin Signaling Pathway.

Cell Physiol Biochem. 2018

[10]
MicroRNA-494 promotes cancer progression and targets adenomatous polyposis coli in colorectal cancer.

Mol Cancer. 2018-1-5

引用本文的文献

[1]
Visceral adipose tissue is associated with occult synchronous peritoneal metastasis in colorectal cancer.

Pleura Peritoneum. 2025-4-24

[2]
Suppressor protein plasma levels and inflammatory indices in colorectal cancer patients.

BMC Cancer. 2025-4-25

[3]
Effect of CDX2 on proliferation, invasion, migration, and apoptosis of duodenal cancer cells.

Eur J Histochem. 2025-4-7

[4]
Unveiling the future of cancer stem cell therapy: a narrative exploration of emerging innovations.

Discov Oncol. 2025-3-22

[5]
Identification of Candidate Alterations Mediating KRASG12C Inhibitor Resistance in Advanced Colorectal and Pancreatic Cancers.

Clin Cancer Res. 2025-3-3

[6]
From silent partners to potential therapeutic targets: macrophages in colorectal cancer.

Cancer Immunol Immunother. 2025-2-25

[7]
miR-1226-5p is involved in radioresistance of colorectal cancer by activating M2 macrophages through suppressing IRF1.

J Transl Med. 2024-10-29

[8]
Arctigenin inhibits the progression of colorectal cancer through epithelial-mesenchymal transition via PI3K/Akt/mTOR signaling pathway.

PLoS One. 2024

[9]
SLC11A1 predicts the overall survival of patients with colorectal cancer.

Am J Cancer Res. 2024-6-15

[10]
Molecular Biomarkers and Signaling Pathways of Cancer Stem Cells in Colorectal Cancer.

Technol Cancer Res Treat. 2024

本文引用的文献

[1]
Colorectal Cancer: The Contribution of CXCL12 and Its Receptors CXCR4 and CXCR7.

Cancers (Basel). 2022-4-2

[2]
Tumor Microenvironment Shapes Colorectal Cancer Progression, Metastasis, and Treatment Responses.

Front Med (Lausanne). 2022-3-23

[3]
Circular RNA ITCH: An Emerging Multifunctional Regulator.

Biomolecules. 2022-2-24

[4]
Diagnostic and therapeutic biomarkers in colorectal cancer: a review.

Am J Cancer Res. 2022-2-15

[5]
Alterations in the Gut Microbiota and Their Metabolites in Colorectal Cancer: Recent Progress and Future Prospects.

Front Oncol. 2022-2-11

[6]
Non-Coding RNAs Regulate the Resistance to Anti-EGFR Therapy in Colorectal Cancer.

Front Oncol. 2022-1-17

[7]
Wnt/β-catenin signaling in colorectal cancer: Is therapeutic targeting even possible?

Biochimie. 2022-4

[8]
Involvement of parathyroid hormone-related peptide in the aggressive phenotype of colorectal cancer cells.

World J Gastroenterol. 2021-11-7

[9]
Recent Updates on Mechanisms of Resistance to 5-Fluorouracil and Reversal Strategies in Colon Cancer Treatment.

Biology (Basel). 2021-8-31

[10]
Toll-Like Receptors (TLRs): Structure, Functions, Signaling, and Role of Their Polymorphisms in Colorectal Cancer Susceptibility.

Biomed Res Int. 2021

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索