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Systemic Mechanisms of Ionic Regulation in Carcinogenesis.

作者信息

Zamay Tatiana N, Zamay Sergey S, Zamay Galina S, Kolovskaya Olga S, Kichkailo Anna S, Berezovski Maxim V

机构信息

Federal Research Center "Krasnoyarsk Science Center" of the Siberian Branch of the Russian Academy of Sciences, Laboratory for Digital Controlled Drugs and Theranostics, Molecular Electronics Department, 660036 Krasnoyarsk, Russia.

Prof. V.F. Voino-Yasenetsky Krasnoyarsk State Medical University Laboratory for Biomolecular and Medical Technologies, 660022 Krasnoyarsk, Russia.

出版信息

Cancers (Basel). 2025 Jan 17;17(2):286. doi: 10.3390/cancers17020286.


DOI:10.3390/cancers17020286
PMID:39858068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11764231/
Abstract

Cancer is a complex disease characterized by uncontrolled cell proliferation at various levels, leading to tumor growth and spread. This review focuses on the role of ion homeostasis in cancer progression. It describes a model of ion-mediated regulation in both normal and cancerous cell proliferation. The main function of this system is to maintain the optimal number of cells in the body by regulating intra- and extracellular ion content. The review discusses the key points of ion regulation and their impact on tumor growth and spread during cancer development. It explains that normal levels of sodium, potassium, calcium, chloride, and hydrogen ions are regulated at different levels. Damage to ion transport mechanisms during carcinogenesis can lead to an increase in sodium cations and water content in cells, disrupting the balance of calcium and hydrogen ions. This, in turn, can lead to chromatin compaction reduction, gene overexpression, and instability at the epigenetic and genomic levels, resulting in increased cell proliferation and mutagenesis. Restoring normal ion balance can reduce the proliferative potential of both normal and tumor cell populations. The proposed model of systemic ionic regulation of proliferation aims to reconcile diverse data related to cell mitotic activity in various physiological conditions and explain tumor growth. Understanding the mechanisms behind pathological cell proliferation is important for developing new approaches to control ion homeostasis in the body, potentially leading to more effective cancer treatment and prevention.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/2695b45fbb62/cancers-17-00286-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/4636f180be1b/cancers-17-00286-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/55e8fedc006b/cancers-17-00286-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/93580a92dfb7/cancers-17-00286-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/2a43143eda2f/cancers-17-00286-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/eec3855aa2c5/cancers-17-00286-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/97c9d59716c2/cancers-17-00286-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/2695b45fbb62/cancers-17-00286-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/4636f180be1b/cancers-17-00286-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/55e8fedc006b/cancers-17-00286-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/93580a92dfb7/cancers-17-00286-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/2a43143eda2f/cancers-17-00286-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/eec3855aa2c5/cancers-17-00286-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/97c9d59716c2/cancers-17-00286-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de8/11764231/2695b45fbb62/cancers-17-00286-g006.jpg

相似文献

[1]
Systemic Mechanisms of Ionic Regulation in Carcinogenesis.

Cancers (Basel). 2025-1-17

[2]
Ion transport in chondrocytes: membrane transporters involved in intracellular ion homeostasis and the regulation of cell volume, free [Ca2+] and pH.

Histol Histopathol. 1998-7

[3]
[Electrolyte and acid-base balance disorders in advanced chronic kidney disease].

Nefrologia. 2008

[4]
Effect of elevated potassium on the ion content of mouse astrocytes and neurons.

Can J Physiol Pharmacol. 1992

[5]
The plasma membrane sodium-hydrogen exchanger and its role in physiological and pathophysiological processes.

Circ Res. 1985-6

[6]
Role of ion channels in gastrointestinal cancer.

World J Gastroenterol. 2019-10-14

[7]
Monovalent ions control proliferation of Ehrlich Lettre ascites cells.

Am J Physiol Cell Physiol. 2010-6-30

[8]
Ion Channel Profiling in Prostate Cancer: Toward Cell Population-Specific Screening.

Rev Physiol Biochem Pharmacol. 2021

[9]
Main Cations and Cellular Biology of Traumatic Spinal Cord Injury.

Cells. 2022-8-11

[10]
Ion transporters in brain tumors.

Curr Med Chem. 2015

本文引用的文献

[1]
Eukaryotic cell size regulation and its implications for cellular function and dysfunction.

Physiol Rev. 2024-10-1

[2]
Application of calcium overload-based ion interference therapy in tumor treatment: strategies, outcomes, and prospects.

Front Pharmacol. 2024-2-15

[3]
Ranolazine: a potential anti-metastatic drug targeting voltage-gated sodium channels.

Br J Cancer. 2024-5

[4]
Inhibition of Na+/H+ exchanger (NHE) 7 by 5-(N-ethyl-N-isopropyl)-Amiloride displays anti-cancer activity in non-small cell lung cancer by disrupting cancer stem cell activity and downregulating PD-L1 expression.

Am J Cancer Res. 2023-10-15

[5]
Effect of Cell Cycle on Cell Surface Expression of Voltage-Gated Sodium Channels and Na,K-ATPase.

Cells. 2022-10-15

[6]
The relationships between growth rate and mitochondrial metabolism varies over time.

Sci Rep. 2022-9-27

[7]
The Role of Targeted Osmotic Lysis in the Treatment of Advanced Carcinoma in Companion Animals: A Case Series.

Case Rep Vet Med. 2022-8-2

[8]
Potassium Channels as a Target for Cancer Therapy: Current Perspectives.

Onco Targets Ther. 2022-7-20

[9]
Na riboswitches regulate genes for diverse physiological processes in bacteria.

Nat Chem Biol. 2022-8

[10]
Alkalization of cellular pH leads to cancer cell death by disrupting autophagy and mitochondrial function.

Oncogene. 2022-7

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