Aspirin Inhibits Brain Metastasis of Lung Cancer via Upregulation of Tight Junction Protein Expression in Microvascular Endothelial Cells

Background: The brain is one of the most vulnerable metastasis sites in lung cancer; approximately 40–50% of lung cancer patients develop brain metastasis during the disease course, contributing to the poor prognosis and high mortality of lung cancer patients. Therefore, it is important to clarify t...

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Main Authors: Dianfang Wei, Ming Tang, Weibo Gong, Jingshuo Liu, Lijuan Qin
Format: Article
Language:English
Published: IMR Press 2023-11-01
Series:Frontiers in Bioscience-Landmark
Subjects:
Online Access:https://www.imrpress.com/journal/FBL/28/11/10.31083/j.fbl2811320
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author Dianfang Wei
Ming Tang
Weibo Gong
Jingshuo Liu
Lijuan Qin
author_facet Dianfang Wei
Ming Tang
Weibo Gong
Jingshuo Liu
Lijuan Qin
author_sort Dianfang Wei
collection DOAJ
description Background: The brain is one of the most vulnerable metastasis sites in lung cancer; approximately 40–50% of lung cancer patients develop brain metastasis during the disease course, contributing to the poor prognosis and high mortality of lung cancer patients. Therefore, it is important to clarify the molecular mechanism underlying brain metastasis of lung cancer for improving the overall survival of lung cancer patients. The present study aimed to investigate the potential role of blood-brain barrier (BBB) permeability in the development of brain metastasis of lung cancer and explore the effect of aspirin in an in-vitro BBB model. Methods: An in-vitro BBB model was established. The expression of heat shock protein 70 (HSP 70), zonula occludens-1 (ZO-1), and occludin in rat brain microvascular endothelial cells was detected using Western blot at different time points following the administration of aspirin. Results: HSP70, ZO-1, and occludin expressions did not show significant changes before aspirin administration, but increased noticeably after aspirin administration. Tumor necrosis factor-α (TNF-α) could significantly attenuate the increased expression of these proteins induced by aspirin. Additionally, TNF-α also significantly reversed the aspirin-induced decrease of BBB permeability. Conclusions: Aspirin may inhibit brain metastasis of lung cancer in a time-dependent manner via upregulating tight junction proteins to reduce BBB permeability, and this effect can be reversed by TNF-α.
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spelling doaj.art-dea6a3f505ee414abfe9b1f1b9a0a9242023-12-08T07:49:20ZengIMR PressFrontiers in Bioscience-Landmark2768-67012023-11-01281132010.31083/j.fbl2811320S2768-6701(23)00997-8Aspirin Inhibits Brain Metastasis of Lung Cancer via Upregulation of Tight Junction Protein Expression in Microvascular Endothelial CellsDianfang Wei0Ming Tang1Weibo Gong2Jingshuo Liu3Lijuan Qin4Department of Basic Medicine, Qilu Medical University, 255300 Zibo, Shandong, ChinaDepartment of Basic Medicine, Qilu Medical University, 255300 Zibo, Shandong, ChinaDepartment of Basic Medicine, Qilu Medical University, 255300 Zibo, Shandong, ChinaDepartment of Basic Medicine, Qilu Medical University, 255300 Zibo, Shandong, ChinaSchool of Basic Medical Sciences, North China University of Science and Technology, 063210 Tangshan, Hebei, ChinaBackground: The brain is one of the most vulnerable metastasis sites in lung cancer; approximately 40–50% of lung cancer patients develop brain metastasis during the disease course, contributing to the poor prognosis and high mortality of lung cancer patients. Therefore, it is important to clarify the molecular mechanism underlying brain metastasis of lung cancer for improving the overall survival of lung cancer patients. The present study aimed to investigate the potential role of blood-brain barrier (BBB) permeability in the development of brain metastasis of lung cancer and explore the effect of aspirin in an in-vitro BBB model. Methods: An in-vitro BBB model was established. The expression of heat shock protein 70 (HSP 70), zonula occludens-1 (ZO-1), and occludin in rat brain microvascular endothelial cells was detected using Western blot at different time points following the administration of aspirin. Results: HSP70, ZO-1, and occludin expressions did not show significant changes before aspirin administration, but increased noticeably after aspirin administration. Tumor necrosis factor-α (TNF-α) could significantly attenuate the increased expression of these proteins induced by aspirin. Additionally, TNF-α also significantly reversed the aspirin-induced decrease of BBB permeability. Conclusions: Aspirin may inhibit brain metastasis of lung cancer in a time-dependent manner via upregulating tight junction proteins to reduce BBB permeability, and this effect can be reversed by TNF-α.https://www.imrpress.com/journal/FBL/28/11/10.31083/j.fbl2811320aspirinlung cancertight junction proteinblood-brain barrierbrain metastasis
spellingShingle Dianfang Wei
Ming Tang
Weibo Gong
Jingshuo Liu
Lijuan Qin
Aspirin Inhibits Brain Metastasis of Lung Cancer via Upregulation of Tight Junction Protein Expression in Microvascular Endothelial Cells
Frontiers in Bioscience-Landmark
aspirin
lung cancer
tight junction protein
blood-brain barrier
brain metastasis
title Aspirin Inhibits Brain Metastasis of Lung Cancer via Upregulation of Tight Junction Protein Expression in Microvascular Endothelial Cells
title_full Aspirin Inhibits Brain Metastasis of Lung Cancer via Upregulation of Tight Junction Protein Expression in Microvascular Endothelial Cells
title_fullStr Aspirin Inhibits Brain Metastasis of Lung Cancer via Upregulation of Tight Junction Protein Expression in Microvascular Endothelial Cells
title_full_unstemmed Aspirin Inhibits Brain Metastasis of Lung Cancer via Upregulation of Tight Junction Protein Expression in Microvascular Endothelial Cells
title_short Aspirin Inhibits Brain Metastasis of Lung Cancer via Upregulation of Tight Junction Protein Expression in Microvascular Endothelial Cells
title_sort aspirin inhibits brain metastasis of lung cancer via upregulation of tight junction protein expression in microvascular endothelial cells
topic aspirin
lung cancer
tight junction protein
blood-brain barrier
brain metastasis
url https://www.imrpress.com/journal/FBL/28/11/10.31083/j.fbl2811320
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