• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
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
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
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 @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

结直肠癌中的信号通路及其对靶向治疗的意义。

Signaling pathways in colorectal cancer implications for the target therapies.

机构信息

Department of Biotherapy, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, No. 17, Block 3, Southern Renmin Road, Chengdu, Sichuan, 610041, People's Republic of China.

West China School of Medicine, West China Hospital, Sichuan University, No. 17, Block 3, Southern Renmin Road, Chengdu, Sichuan, 610041, People's Republic of China.

出版信息

Mol Biomed. 2024 Jun 7;5(1):21. doi: 10.1186/s43556-024-00178-y.

DOI:10.1186/s43556-024-00178-y
PMID:38844562
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11156834/
Abstract

Colorectal carcinoma (CRC) stands as a pressing global health issue, marked by the unbridled proliferation of immature cells influenced by multifaceted internal and external factors. Numerous studies have explored the intricate mechanisms of tumorigenesis in CRC, with a primary emphasis on signaling pathways, particularly those associated with growth factors and chemokines. However, the sheer diversity of molecular targets introduces complexity into the selection of targeted therapies, posing a significant challenge in achieving treatment precision. The quest for an effective CRC treatment is further complicated by the absence of pathological insights into the mutations or alterations occurring in tumor cells. This study reveals the transfer of signaling from the cell membrane to the nucleus, unveiling recent advancements in this crucial cellular process. By shedding light on this novel dimension, the research enhances our understanding of the molecular intricacies underlying CRC, providing a potential avenue for breakthroughs in targeted therapeutic strategies. In addition, the study comprehensively outlines the potential immune responses incited by the aberrant activation of signaling pathways, with a specific focus on immune cells, cytokines, and their collective impact on the dynamic landscape of drug development. This research not only contributes significantly to advancing CRC treatment and molecular medicine but also lays the groundwork for future breakthroughs and clinical trials, fostering optimism for improved outcomes and refined approaches in combating colorectal carcinoma.

摘要

结直肠癌(CRC)是一个全球性的健康问题,其特征是不成熟细胞不受控制地增殖,这受到多种内部和外部因素的影响。许多研究已经探讨了结直肠癌的肿瘤发生的复杂机制,主要集中在信号通路,特别是与生长因子和趋化因子相关的信号通路。然而,分子靶点的多样性使得靶向治疗的选择变得复杂,在实现治疗精确性方面带来了重大挑战。由于缺乏对肿瘤细胞中发生的突变或改变的病理见解,有效的 CRC 治疗方法的探索变得更加复杂。这项研究揭示了信号从细胞膜向细胞核的传递,揭示了这一关键细胞过程的最新进展。通过揭示这一新的维度,该研究增强了我们对 CRC 分子复杂性的理解,为靶向治疗策略的突破提供了潜在途径。此外,该研究全面概述了信号通路异常激活引发的潜在免疫反应,特别关注免疫细胞、细胞因子及其对药物开发动态景观的集体影响。这项研究不仅对推进 CRC 治疗和分子医学具有重要意义,也为未来的突破和临床试验奠定了基础,为改善结直肠癌的治疗效果和方法带来了乐观前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/125e9931ce25/43556_2024_178_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/52264dc0d033/43556_2024_178_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/02f3c4ea8ed6/43556_2024_178_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/8e6bd7af7477/43556_2024_178_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/a2f60d07f9cc/43556_2024_178_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/1283acbc718f/43556_2024_178_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/125e9931ce25/43556_2024_178_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/52264dc0d033/43556_2024_178_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/02f3c4ea8ed6/43556_2024_178_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/8e6bd7af7477/43556_2024_178_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/a2f60d07f9cc/43556_2024_178_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/1283acbc718f/43556_2024_178_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dee5/11156834/125e9931ce25/43556_2024_178_Fig6_HTML.jpg

相似文献

1
Signaling pathways in colorectal cancer implications for the target therapies.结直肠癌中的信号通路及其对靶向治疗的意义。
Mol Biomed. 2024 Jun 7;5(1):21. doi: 10.1186/s43556-024-00178-y.
2
Novel targeting approaches and signaling pathways of colorectal cancer: An insight.结直肠癌的新型靶向方法和信号通路:一个新视角。
World J Gastroenterol. 2018 Oct 21;24(39):4428-4435. doi: 10.3748/wjg.v24.i39.4428.
3
Signaling pathways involved in colorectal cancer: pathogenesis and targeted therapy.涉及结直肠癌的信号通路:发病机制和靶向治疗。
Signal Transduct Target Ther. 2024 Oct 7;9(1):266. doi: 10.1038/s41392-024-01953-7.
4
Therapeutic strategies targeting Wnt/β‑catenin signaling for colorectal cancer (Review).靶向结直肠癌 Wnt/β-连环蛋白信号通路的治疗策略(综述)。
Int J Mol Med. 2022 Jan;49(1). doi: 10.3892/ijmm.2021.5056. Epub 2021 Oct 29.
5
Deciphering the functional landscape and therapeutic implications of noncoding RNAs in the TGF-β signaling pathway in colorectal cancer: A comprehensive review.解读非编码RNA在结直肠癌转化生长因子-β信号通路中的功能格局及治疗意义:一项综述
Pathol Res Pract. 2024 Mar;255:155158. doi: 10.1016/j.prp.2024.155158. Epub 2024 Jan 22.
6
Novel and Emerging Targeted Therapies of Colorectal Cancer.结直肠癌的新型及新兴靶向治疗
Curr Clin Pharmacol. 2015;10(4):279-98. doi: 10.2174/1574884710666151020095911.
7
Molecular Targets in Precision Chemoprevention of Colorectal Cancer: An Update from Pre-Clinical to Clinical Trials.精准化学预防结直肠癌的分子靶点:从临床前到临床试验的最新进展。
Int J Mol Sci. 2020 Dec 17;21(24):9609. doi: 10.3390/ijms21249609.
8
From Molecular Biology to Clinical Trials: Toward Personalized Colorectal Cancer Therapy.从分子生物学到临床试验:迈向个性化结直肠癌治疗
Clin Colorectal Cancer. 2016 Jun;15(2):104-15. doi: 10.1016/j.clcc.2015.11.001. Epub 2015 Dec 2.
9
Epidermal growth factor receptor: pathway, therapies, and pipeline.表皮生长因子受体:通路、治疗方法和研发管线。
Clin Ther. 2013 Sep;35(9):1282-303. doi: 10.1016/j.clinthera.2013.08.007.
10
Targeting cancer stem-like cells in glioblastoma and colorectal cancer through metabolic pathways.通过代谢途径靶向胶质母细胞瘤和结直肠癌中的癌症干细胞样细胞。
Int J Cancer. 2017 Jan 1;140(1):10-22. doi: 10.1002/ijc.30259. Epub 2016 Jul 20.

引用本文的文献

1
The effectiveness of three months EGFR-CTH therapy in palliative colorectal cancer.三个月的表皮生长因子受体-循环肿瘤细胞疗法对晚期结直肠癌的疗效
Rep Pract Oncol Radiother. 2025 Aug 7;30(3):357-365. doi: 10.5603/rpor.106280. eCollection 2025.
2
From Mutation to Prognosis: AI-HOPE-PI3K Enables Artificial Intelligence Agent-Driven Integration of PI3K Pathway Data in Colorectal Cancer Precision Medicine.从突变到预后:AI-HOPE-PI3K助力人工智能驱动的PI3K通路数据在结直肠癌精准医学中的整合
Int J Mol Sci. 2025 Jul 5;26(13):6487. doi: 10.3390/ijms26136487.
3
KLHL5 Contributes to Colorectal Cancer Cell Survival by Promoting Cell Cycle Progression and Suppressing Apoptotic Cell Death.

本文引用的文献

1
Genome-wide characterization of the TGF-β gene family and their expression in different tissues during tail regeneration in the Schlegel's Japanese gecko Gekko japonicus.基因组范围内鉴定 TGF-β 基因家族及其在 Schlegel 的日本壁虎 Gekko japonicus 尾部再生过程中不同组织中的表达。
Int J Biol Macromol. 2024 Jan;255:128127. doi: 10.1016/j.ijbiomac.2023.128127. Epub 2023 Nov 19.
2
Vactosertib potently improves anti-tumor properties of 5-FU for colon cancer.伏他西特联合氟尿嘧啶显著改善结肠癌的抗肿瘤特性。
Daru. 2023 Dec;31(2):193-203. doi: 10.1007/s40199-023-00474-y. Epub 2023 Sep 23.
3
TGF-β signaling in health and disease.
KLHL5通过促进细胞周期进程和抑制凋亡性细胞死亡来促进结肠癌细胞存活。
Cancer Sci. 2025 Sep;116(9):2444-2456. doi: 10.1111/cas.70108. Epub 2025 Jul 1.
4
Constructing Cell-Specific Causal Networks of Individual Cells for Depicting Dynamical Biological Processes.构建单个细胞的细胞特异性因果网络以描绘动态生物学过程。
Research (Wash D C). 2025 Jun 27;8:0743. doi: 10.34133/research.0743. eCollection 2025.
5
RSU1 Mediates Caco-2 Colorectal Cancer Cells Proliferation and Migration via PI3K/AKT Signaling Pathway.RSU1通过PI3K/AKT信号通路介导Caco-2结肠癌细胞的增殖和迁移。
Cell Biochem Biophys. 2025 Jun 21. doi: 10.1007/s12013-025-01809-z.
6
Signalomics for molecular tumor boards and precision oncology of breast and gynecological cancers.用于分子肿瘤委员会以及乳腺癌和妇科癌症精准肿瘤学的信号组学。
Mol Syst Biol. 2025 Jun 9. doi: 10.1038/s44320-025-00125-1.
7
A computed tomography-based radiomics prediction model for BRAF mutation status in colorectal cancer.一种基于计算机断层扫描的结直肠癌BRAF突变状态的影像组学预测模型。
Abdom Radiol (NY). 2025 May 15. doi: 10.1007/s00261-025-04983-z.
8
Eudragit S 100 Assisted Molecular Solid Dispersion of Andrographolide Tendered Augmented Drug Delivery and Apoptosis in Human Colon Cancer, HT-29 Cells.Eudragit S 100辅助的穿心莲内酯分子固体分散体促进了人结肠癌HT-29细胞中的药物递送增强及细胞凋亡。
AAPS PharmSciTech. 2025 Mar 11;26(3):82. doi: 10.1208/s12249-025-03073-z.
9
Colorectal Cancer: Current and Future Therapeutic Approaches and Related Technologies Addressing Multidrug Strategies Against Multiple Level Resistance Mechanisms.结直肠癌:针对多重耐药机制的多药策略的当前及未来治疗方法和相关技术
Int J Mol Sci. 2025 Feb 4;26(3):1313. doi: 10.3390/ijms26031313.
10
Alternative Splicing at the Crossroad of Inflammatory Bowel Diseases and Colitis-Associated Colon Cancer.炎症性肠病与结肠炎相关结肠癌交叉路口的可变剪接
Cancers (Basel). 2025 Jan 11;17(2):219. doi: 10.3390/cancers17020219.
转化生长因子-β 信号在健康和疾病中的作用。
Cell. 2023 Sep 14;186(19):4007-4037. doi: 10.1016/j.cell.2023.07.036.
4
A Phase I Study of the Pan-Notch Inhibitor CB-103 for Patients with Advanced Adenoid Cystic Carcinoma and Other Tumors.一项针对晚期腺样囊性癌和其他肿瘤患者的泛 Notch 抑制剂 CB-103 的 I 期研究。
Cancer Res Commun. 2023 Sep 14;3(9):1853-1861. doi: 10.1158/2767-9764.CRC-23-0333.
5
SMAD Proteins in TGF-β Signalling Pathway in Cancer: Regulatory Mechanisms and Clinical Applications.癌症中TGF-β信号通路中的SMAD蛋白:调控机制与临床应用
Diagnostics (Basel). 2023 Aug 26;13(17):2769. doi: 10.3390/diagnostics13172769.
6
Targeting transforming growth factor beta (TGF-β) using Pirfenidone, a potential repurposing therapeutic strategy in colorectal cancer.靶向转化生长因子β(TGF-β)的吡非尼酮,一种结直肠癌潜在的再利用治疗策略。
Sci Rep. 2023 Sep 1;13(1):14357. doi: 10.1038/s41598-023-41550-2.
7
MHC Class II is Induced by IFNγ and Follows Three Distinct Patterns of Expression in Colorectal Cancer Organoids.MHC Ⅱ类分子由 IFNγ诱导,并在结直肠类器官中呈现三种不同的表达模式。
Cancer Res Commun. 2023 Aug 9;3(8):1501-1513. doi: 10.1158/2767-9764.CRC-23-0091. eCollection 2023 Aug.
8
Loss of Pkd1 limits susceptibility to colitis and colorectal cancer.多囊蛋白1的缺失限制了对结肠炎和结直肠癌的易感性。
Oncogenesis. 2023 Aug 5;12(1):40. doi: 10.1038/s41389-023-00486-y.
9
Peripheral Neuron-Organoid Interaction Induces Colonic Epithelial Differentiation via Non-Synaptic Substance P Secretion.外周神经元-类器官相互作用通过非突触性P物质分泌诱导结肠上皮分化。
Int J Stem Cells. 2023 Aug 30;16(3):269-280. doi: 10.15283/ijsc23026. Epub 2023 Jun 30.
10
Using patient-derived tumor organoids from common epithelial cancers to analyze personalized T-cell responses to neoantigens.利用源自常见上皮癌的患者源性肿瘤类器官分析新抗原的个体化 T 细胞反应。
Cancer Immunol Immunother. 2023 Oct;72(10):3149-3162. doi: 10.1007/s00262-023-03476-6. Epub 2023 Jun 27.