Arteannuin B Inhibits <scp>NSCLC</scp> Cells via Regulating <scp>miR</scp> ‐194‐3p/ <scp> <i>CLDN2</i> </scp> Axis

Arteannuin B (Art B), a sesquiterpene lactone from Artemisia annua, combats non-small cell lung cancer (NSCLC) chemoresistance by activating a novel miR-194-3p/CLDN2 axis, as identified here through integrated transcriptomic and functional analyses. Here, we combined transcriptomic profiling with functional validation to identify claudin-2 (CLDN2) as a critical mediator of Art B's anticancer effects in NSCLC. CLDN2, significantly upregulated in NSCLC tissues versus paired normal tissues, promoted tumor cell proliferation and cisplatin resistance by upregulating multidrug resistance-associated protein 2 (MRP2). Mechanistically, miR-194-3p directly binds to two conserved sites (nt 358-365 and 1232-1238) within the CLDN2 3' UTR, suppressing its expression via mRNA degradation and translational inhibition, thereby attenuating proliferation and resensitizing cells to cisplatin. Importantly, Art B exerted antitumor effects by upregulating miR-194-3p, which subsequently inhibited CLDN2. This study not only elucidates a previously unrecognized mechanism for overcoming chemoresistance but also nominates CLDN2 as a prognostic biomarker, offering a promising therapeutic strategy that could benefit NSCLC patients facing treatment failure.

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Publication Details

Journal
Cancer Medicine
Published
2026-04-01
DOI
https://doi.org/10.1002/cam4.71796
Primary Topic
Barrier Structure and Function Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Arteannuin B Inhibits NSCLC Cells via Regulating miR ‐194‐3p/ CLDN2 Axis

Wei Huang, Tingsha He, X D Li, Rong-Hui Chen et al.
Cancer Medicine
Barrier Structure and Function Studies
article

Arteannuin B Inhibits NSCLC Cells via Regulating miR ‐194‐3p/ CLDN2 Axis

Wei Huang, Tingsha He, X D Li, Rong-Hui Chen, Rongmin Yu, Jiahui Han, Jing Feng, Qiang Zhang, Tian‐Ze Chen, Li‐Yan Song
article en

Abstract

Arteannuin B (Art B), a sesquiterpene lactone from Artemisia annua, combats non-small cell lung cancer (NSCLC) chemoresistance by activating a novel miR-194-3p/CLDN2 axis, as identified here through integrated transcriptomic and functional analyses. Here, we combined transcriptomic profiling with functional validation to identify claudin-2 (CLDN2) as a critical mediator of Art B's anticancer effects in NSCLC. CLDN2, significantly upregulated in NSCLC tissues versus paired normal tissues, promoted tumor cell proliferation and cisplatin resistance by upregulating multidrug resistance-associated protein 2 (MRP2). Mechanistically, miR-194-3p directly binds to two conserved sites (nt 358-365 and 1232-1238) within the CLDN2 3' UTR, suppressing its expression via mRNA degradation and translational inhibition, thereby attenuating proliferation and resensitizing cells to cisplatin. Importantly, Art B exerted antitumor effects by upregulating miR-194-3p, which subsequently inhibited CLDN2. This study not only elucidates a previously unrecognized mechanism for overcoming chemoresistance but also nominates CLDN2 as a prognostic biomarker, offering a promising therapeutic strategy that could benefit NSCLC patients facing treatment failure.

Cancer MedicineVol. 15(4)
Guangzhou University of Chinese Medicine (CN), Jinan University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Guangdong Province
Good health and well-being
Openalex Percentile: Top 24%
Barrier Structure and Function Studies
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Arteannuin B Inhibits <scp>NSCLC</scp> Cells via Regulating <scp>miR</scp> ‐194‐3p/ <scp> <i>CLDN2</i> </scp> Axis — Wei Huang, Tingsha He, et al. · Cancer Medicine (2026) | TGRS Research Map | TGRS