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神经酰胺如何影响结肠癌的发展:从正常结肠到癌。

How ceramides affect the development of colon cancer: from normal colon to carcinoma.

机构信息

Goethe-University Frankfurt, Institute of Clinical Pharmacology, Theodor Stern Kai 7, 60590, Frankfurt, Germany.

Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Theodor-Stern-Kai 7, 60596, Frankfurt Am Main, Germany.

出版信息

Pflugers Arch. 2024 Dec;476(12):1803-1816. doi: 10.1007/s00424-024-02960-x. Epub 2024 Apr 18.


DOI:10.1007/s00424-024-02960-x
PMID:38635059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11582153/
Abstract

The integrity of the colon and the development of colon cancer depend on the sphingolipid balance in colon epithelial cells. In this review, we summarize the current knowledge on how ceramides and their complex derivatives influence normal colon development and colon cancer development. Ceramides, glucosylceramides and sphingomyelin are essential membrane components and, due to their biophysical properties, can influence the activation of membrane proteins, affecting protein-protein interactions and downstream signalling pathways. Here, we review the cellular mechanisms known to be affected by ceramides and their effects on colon development. We also describe which ceramides are deregulated during colorectal carcinogenesis, the molecular mechanisms involved in ceramide deregulation and how this affects carcinogenesis. Finally, we review new methods that are now state of the art for studying lipid-protein interactions in the physiological environment.

摘要

结肠的完整性和结肠癌的发展取决于结肠上皮细胞中的鞘脂平衡。在这篇综述中,我们总结了目前关于神经酰胺及其复杂衍生物如何影响正常结肠发育和结肠癌发展的知识。神经酰胺、葡萄糖神经酰胺和神经鞘磷脂是必需的膜成分,由于它们的物理特性,能够影响膜蛋白的激活,影响蛋白质-蛋白质相互作用和下游信号通路。在这里,我们综述了已知受神经酰胺影响的细胞机制及其对结肠发育的影响。我们还描述了在结直肠癌变过程中哪些神经酰胺失调,神经酰胺失调涉及的分子机制以及这如何影响癌变。最后,我们综述了目前用于研究生理环境中脂-蛋白相互作用的最新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/b9800aed4a4c/424_2024_2960_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/8a0b42a5a5c6/424_2024_2960_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/3d62d78936ec/424_2024_2960_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/f456ba2d6d5a/424_2024_2960_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/38250c4534a6/424_2024_2960_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/b9800aed4a4c/424_2024_2960_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/8a0b42a5a5c6/424_2024_2960_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/3d62d78936ec/424_2024_2960_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/f456ba2d6d5a/424_2024_2960_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/38250c4534a6/424_2024_2960_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11582153/b9800aed4a4c/424_2024_2960_Fig5_HTML.jpg

相似文献

[1]
How ceramides affect the development of colon cancer: from normal colon to carcinoma.

Pflugers Arch. 2024-12

[2]
Anticancer compounds and sphingolipid metabolism in the colon.

In Vivo. 2005

[3]
Ceramide: a simple sphingolipid with unique biophysical properties.

Prog Lipid Res. 2014-2-7

[4]
Role of neutral ceramidase in colon cancer.

FASEB J. 2016-12

[5]
Ceramide signalling: regulatory role in cell proliferation, differentiation and apoptosis in human epidermis.

Arch Dermatol Res. 1997-9

[6]
Cyclooxygenase-2 inhibition sensitizes human colon carcinoma cells to TRAIL-induced apoptosis through clustering of DR5 and concentrating death-inducing signaling complex components into ceramide-enriched caveolae.

Cancer Res. 2005-12-15

[7]
Diverse Sphingolipid Profiles in Rectal and Colon Cancer.

Int J Mol Sci. 2023-6-29

[8]
Sphingosine kinase isoforms regulate oxaliplatin sensitivity of human colon cancer cells through ceramide accumulation and Akt activation.

J Biol Chem. 2009-4-17

[9]
Expression of Ceramide Synthase 6 Transcriptionally Activates Acid Ceramidase in a c-Jun N-terminal Kinase (JNK)-dependent Manner.

J Biol Chem. 2015-5-22

[10]
Ablation of ceramide synthase 2 exacerbates dextran sodium sulphate-induced colitis in mice due to increased intestinal permeability.

J Cell Mol Med. 2017-7-12

引用本文的文献

[1]
A Comprehensive Review on the Molecular Mechanism of Lycopene in Cancer Therapy.

Food Sci Nutr. 2025-7-13

[2]
Lipid signaling: facets of a versatile cell communication strategy in health and disease.

Pflugers Arch. 2024-12

本文引用的文献

[1]
Hypoxia induced deregulation of sphingolipids in colon cancer is a prognostic marker for patient outcome.

Biochim Biophys Acta Mol Basis Dis. 2024-1

[2]
Ceramide synthase CERS4 gene downregulation is associated with KRAS mutation in colorectal cancer.

Sci Rep. 2023-9-27

[3]
Staging of colorectal cancer using lipid biomarkers and machine learning.

Metabolomics. 2023-9-20

[4]
NLRP12 downregulates the Wnt/β-catenin pathway via interaction with STK38 to suppress colorectal cancer.

J Clin Invest. 2023-10-2

[5]
Ceramides Increase Fatty Acid Utilization in Intestinal Progenitors to Enhance Stemness and Increase Tumor Risk.

Gastroenterology. 2023-11

[6]
Diverse Sphingolipid Profiles in Rectal and Colon Cancer.

Int J Mol Sci. 2023-6-29

[7]
Establishment of gastrointestinal assembloids to study the interplay between epithelial crypts and their mesenchymal niche.

Nat Commun. 2023-5-25

[8]
Activated EGFR and PDGFR internalize in separate vesicles and downstream AKT and ERK1/2 signaling are differentially impacted by cholesterol depletion.

Biochem Biophys Res Commun. 2023-7-12

[9]
MYC-activated CERS6-AS1 sponges miR-6838-5p and regulates the expression of RUBCNL in colorectal cancer.

Cell Mol Biol (Noisy-le-grand). 2022-12-31

[10]
Genome-wide identification of A-to-I RNA editing events provides the functional implications in PDAC.

Front Oncol. 2023-2-21

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