Tight junction proteins in glial tumors development and progression

Tight junctions form a paracellular barrier in epithelial and endothelial cells, and they regulate the diffusion of fluids, molecules, and the penetration of cells across tissue compartments. Tight junctions are composed of a group of integral membrane proteins, which include the claudin family, tig...

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Main Authors: Jakub Moskal, Slawomir Michalak
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-02-01
Series:Frontiers in Cellular Neuroscience
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Online Access:https://www.frontiersin.org/articles/10.3389/fncel.2025.1541885/full
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author Jakub Moskal
Slawomir Michalak
Slawomir Michalak
author_facet Jakub Moskal
Slawomir Michalak
Slawomir Michalak
author_sort Jakub Moskal
collection DOAJ
description Tight junctions form a paracellular barrier in epithelial and endothelial cells, and they regulate the diffusion of fluids, molecules, and the penetration of cells across tissue compartments. Tight junctions are composed of a group of integral membrane proteins, which include the claudin family, tight junction-associated Marvel protein family, junctional adhesion molecule family, and proteins that anchor the cytoskeleton, such as zonula occludens proteins and the cingulin family. Several factors, such as neurotransmitters or cytokines, and processes like ischemia/hypoxia, inflammation, tumorigenesis, phosphorylation/dephosphorylation, ubiquitination, and palmitoylation, regulate tight junction proteins. Claudins are involved in tumorigenesis processes that lead to glioma formation. In gliomas, there is a noticeable dysregulation of claudins, occludin, and zonula occludens-1 abundance, and their dislocation has been observed. The weakening of intercellular adhesion and cell detachment is responsible for glioma infiltration into surrounding tissues. Furthermore, the paracellular permeability of the blood–brain barrier, formed with the involvement of tight junction proteins, influences the development of peritumoral edema – and, simultaneously, the rate of drug delivery to the glial tumor. Understanding the junctional and paracellular environments in brain tumors is crucial to predicting glial tumor progression and the feasibility of chemotherapeutic drug delivery. This knowledge may also illuminate differences between high and low-grade gliomas.
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spelling doaj-art-4758d77af178402a80b7a3c7952922d82025-02-03T06:33:49ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022025-02-011910.3389/fncel.2025.15418851541885Tight junction proteins in glial tumors development and progressionJakub Moskal0Slawomir Michalak1Slawomir Michalak2Department of Neurosurgery and Neurotraumatology, Poznan University of Medical Sciences, Poznan, PolandDepartment of Neurosurgery and Neurotraumatology, Poznan University of Medical Sciences, Poznan, PolandDepartment of Neurochemistry and Neuropathology, Poznan University of Medical Sciences, Poznan, PolandTight junctions form a paracellular barrier in epithelial and endothelial cells, and they regulate the diffusion of fluids, molecules, and the penetration of cells across tissue compartments. Tight junctions are composed of a group of integral membrane proteins, which include the claudin family, tight junction-associated Marvel protein family, junctional adhesion molecule family, and proteins that anchor the cytoskeleton, such as zonula occludens proteins and the cingulin family. Several factors, such as neurotransmitters or cytokines, and processes like ischemia/hypoxia, inflammation, tumorigenesis, phosphorylation/dephosphorylation, ubiquitination, and palmitoylation, regulate tight junction proteins. Claudins are involved in tumorigenesis processes that lead to glioma formation. In gliomas, there is a noticeable dysregulation of claudins, occludin, and zonula occludens-1 abundance, and their dislocation has been observed. The weakening of intercellular adhesion and cell detachment is responsible for glioma infiltration into surrounding tissues. Furthermore, the paracellular permeability of the blood–brain barrier, formed with the involvement of tight junction proteins, influences the development of peritumoral edema – and, simultaneously, the rate of drug delivery to the glial tumor. Understanding the junctional and paracellular environments in brain tumors is crucial to predicting glial tumor progression and the feasibility of chemotherapeutic drug delivery. This knowledge may also illuminate differences between high and low-grade gliomas.https://www.frontiersin.org/articles/10.3389/fncel.2025.1541885/fulltight junctionclaudin familyTJ-associated Marvel protein familyjunctional adhesion molecule familyzonula occludens proteinglial tumors
spellingShingle Jakub Moskal
Slawomir Michalak
Slawomir Michalak
Tight junction proteins in glial tumors development and progression
Frontiers in Cellular Neuroscience
tight junction
claudin family
TJ-associated Marvel protein family
junctional adhesion molecule family
zonula occludens protein
glial tumors
title Tight junction proteins in glial tumors development and progression
title_full Tight junction proteins in glial tumors development and progression
title_fullStr Tight junction proteins in glial tumors development and progression
title_full_unstemmed Tight junction proteins in glial tumors development and progression
title_short Tight junction proteins in glial tumors development and progression
title_sort tight junction proteins in glial tumors development and progression
topic tight junction
claudin family
TJ-associated Marvel protein family
junctional adhesion molecule family
zonula occludens protein
glial tumors
url https://www.frontiersin.org/articles/10.3389/fncel.2025.1541885/full
work_keys_str_mv AT jakubmoskal tightjunctionproteinsinglialtumorsdevelopmentandprogression
AT slawomirmichalak tightjunctionproteinsinglialtumorsdevelopmentandprogression
AT slawomirmichalak tightjunctionproteinsinglialtumorsdevelopmentandprogression