Aloe-emodin mediates the inhibitory effect of LncRNA D63785 on the PI3K/Akt/mTOR pathway in nasopharyngeal carcinoma

BackgroundLong non-coding RNAs (lncRNAs) are dysregulated in nasopharyngeal carcinoma (NPC), yet their interplay with pharmacological agents like aloe-emodin (AE) remains unclear. This study explores AE’s anti-NPC mechanisms via lncRNA D63785 and the PI3K/Akt/mTOR pathway.MethodsNPC cells (CNE1, C66...

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Main Authors: Min He, Lei Xie, Jiayi Huang, Han Su, Jiahua Hu, Liuping Xie, Mengqin Li, Xin Zeng, Jianhong Tang
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-07-01
Series:Frontiers in Pharmacology
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Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2025.1573408/full
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author Min He
Lei Xie
Lei Xie
Jiayi Huang
Han Su
Jiahua Hu
Liuping Xie
Liuping Xie
Mengqin Li
Mengqin Li
Xin Zeng
Xin Zeng
Jianhong Tang
Jianhong Tang
Jianhong Tang
author_facet Min He
Lei Xie
Lei Xie
Jiayi Huang
Han Su
Jiahua Hu
Liuping Xie
Liuping Xie
Mengqin Li
Mengqin Li
Xin Zeng
Xin Zeng
Jianhong Tang
Jianhong Tang
Jianhong Tang
author_sort Min He
collection DOAJ
description BackgroundLong non-coding RNAs (lncRNAs) are dysregulated in nasopharyngeal carcinoma (NPC), yet their interplay with pharmacological agents like aloe-emodin (AE) remains unclear. This study explores AE’s anti-NPC mechanisms via lncRNA D63785 and the PI3K/Akt/mTOR pathway.MethodsNPC cells (CNE1, C666-1) were treated with AE, followed by qRT-PCR and Western blotting to assess lncRNA D63785 and PI3K/Akt/mTOR pathway proteins. siRNA-mediated lncRNA D63785 knockdown combined with functional assays (CCK-8, EdU, colony/wound-healing) evaluated AE’s effects on proliferation, migration, and pathway activity. In vivo validation used nude mouse xenografts.ResultsLncRNA D63785 was overexpressed in NPC cells (p < 0.01). AE suppressed lncRNA D63785 expression, concurrently reducing PI3K/Akt/mTOR phosphorylation (p < 0.05). siRNA knockdown partially reversed AE’s inhibition of NPC cell viability, proliferation, and migration. In vivo, AE attenuated tumor growth (p < 0.05), correlating with lncRNA D63785 downregulation and PI3K/Akt/mTOR dephosphorylation.ConclusionAE exerts anti-NPC effects by targeting the lncRNA D63785-PI3K/Akt/mTOR axis, offering a novel therapeutic strategy. These findings bridge AE’s pharmacological activity with lncRNA regulatory networks in NPC pathogenesis.
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spelling doaj-art-9532f5af9f6a4f24aa99b5b8aeb23dba2025-08-20T03:51:09ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122025-07-011610.3389/fphar.2025.15734081573408Aloe-emodin mediates the inhibitory effect of LncRNA D63785 on the PI3K/Akt/mTOR pathway in nasopharyngeal carcinomaMin He0Lei Xie1Lei Xie2Jiayi Huang3Han Su4Jiahua Hu5Liuping Xie6Liuping Xie7Mengqin Li8Mengqin Li9Xin Zeng10Xin Zeng11Jianhong Tang12Jianhong Tang13Jianhong Tang14Department of Pharmacy, The Second Affiliated Hospital of Guilin Medical University, Guilin, ChinaCollege of Pharmacy, Guilin Medical University, Guilin, ChinaGuangxi Key Laboratory of Diabetic Systems Medicine, Guilin Medical University, Guilin, ChinaDepartment of Traditional Chinese Medicine, The Second Affiliated Hospital of Guilin Medical University, Guilin, ChinaDepartment of Neurology, The Affiliated Hospital of Guilin Medical University, Guilin, ChinaCentral Laboratory, Guangxi Health Commission Key Laboratory of Glucose and Lipid Metabolism Disorders, The Second Affiliated Hospital of Guilin Medical University, Guilin, ChinaCollege of Pharmacy, Guilin Medical University, Guilin, ChinaGuangxi Key Laboratory of Diabetic Systems Medicine, Guilin Medical University, Guilin, ChinaCollege of Pharmacy, Guilin Medical University, Guilin, ChinaGuangxi Key Laboratory of Diabetic Systems Medicine, Guilin Medical University, Guilin, ChinaCollege of Pharmacy, Guilin Medical University, Guilin, ChinaGuangxi Key Laboratory of Diabetic Systems Medicine, Guilin Medical University, Guilin, ChinaDepartment of Pharmacy, The Second Affiliated Hospital of Guilin Medical University, Guilin, ChinaGuangxi Health Commission Key Laboratory of Glucose and Lipid Metabolism Disorders, The Second Affiliated Hospital of Guilin Medical University, Guilin, ChinaSchool of General Medical, Guilin Medical University, Guilin, ChinaBackgroundLong non-coding RNAs (lncRNAs) are dysregulated in nasopharyngeal carcinoma (NPC), yet their interplay with pharmacological agents like aloe-emodin (AE) remains unclear. This study explores AE’s anti-NPC mechanisms via lncRNA D63785 and the PI3K/Akt/mTOR pathway.MethodsNPC cells (CNE1, C666-1) were treated with AE, followed by qRT-PCR and Western blotting to assess lncRNA D63785 and PI3K/Akt/mTOR pathway proteins. siRNA-mediated lncRNA D63785 knockdown combined with functional assays (CCK-8, EdU, colony/wound-healing) evaluated AE’s effects on proliferation, migration, and pathway activity. In vivo validation used nude mouse xenografts.ResultsLncRNA D63785 was overexpressed in NPC cells (p < 0.01). AE suppressed lncRNA D63785 expression, concurrently reducing PI3K/Akt/mTOR phosphorylation (p < 0.05). siRNA knockdown partially reversed AE’s inhibition of NPC cell viability, proliferation, and migration. In vivo, AE attenuated tumor growth (p < 0.05), correlating with lncRNA D63785 downregulation and PI3K/Akt/mTOR dephosphorylation.ConclusionAE exerts anti-NPC effects by targeting the lncRNA D63785-PI3K/Akt/mTOR axis, offering a novel therapeutic strategy. These findings bridge AE’s pharmacological activity with lncRNA regulatory networks in NPC pathogenesis.https://www.frontiersin.org/articles/10.3389/fphar.2025.1573408/fullAENPCLncRNA D63785PI3K/Akt/mTOR signaling pathwayproliferation and migration
spellingShingle Min He
Lei Xie
Lei Xie
Jiayi Huang
Han Su
Jiahua Hu
Liuping Xie
Liuping Xie
Mengqin Li
Mengqin Li
Xin Zeng
Xin Zeng
Jianhong Tang
Jianhong Tang
Jianhong Tang
Aloe-emodin mediates the inhibitory effect of LncRNA D63785 on the PI3K/Akt/mTOR pathway in nasopharyngeal carcinoma
Frontiers in Pharmacology
AE
NPC
LncRNA D63785
PI3K/Akt/mTOR signaling pathway
proliferation and migration
title Aloe-emodin mediates the inhibitory effect of LncRNA D63785 on the PI3K/Akt/mTOR pathway in nasopharyngeal carcinoma
title_full Aloe-emodin mediates the inhibitory effect of LncRNA D63785 on the PI3K/Akt/mTOR pathway in nasopharyngeal carcinoma
title_fullStr Aloe-emodin mediates the inhibitory effect of LncRNA D63785 on the PI3K/Akt/mTOR pathway in nasopharyngeal carcinoma
title_full_unstemmed Aloe-emodin mediates the inhibitory effect of LncRNA D63785 on the PI3K/Akt/mTOR pathway in nasopharyngeal carcinoma
title_short Aloe-emodin mediates the inhibitory effect of LncRNA D63785 on the PI3K/Akt/mTOR pathway in nasopharyngeal carcinoma
title_sort aloe emodin mediates the inhibitory effect of lncrna d63785 on the pi3k akt mtor pathway in nasopharyngeal carcinoma
topic AE
NPC
LncRNA D63785
PI3K/Akt/mTOR signaling pathway
proliferation and migration
url https://www.frontiersin.org/articles/10.3389/fphar.2025.1573408/full
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