A1 Refereed original research article in a scientific journal

Artesunate Nanoplatform Targets the Serine–MAPK Axis in Cancer‐Associated Fibroblasts to Reverse Photothermal Resistance in Triple‐Negative Breast Cancer




AuthorsZheng, Dongdong; Yan, Jiaqi; Liu, Xuejiao; Zhang, Zhiming; Jin, Anqi; Zhao, Yue; Bai, Lu; Quan, Mengyao; Qi, Xiuzhu; Fu, Bin; Wu, Zhigang; Zhou, Jin; Han, Han; Wang, Ziqi; Wang, Shiyu; Deng, Chaoqiang; Sun, Weijian; Chang, Cai; Zhou, Shichong; Zhang, Hongbo

PublisherWiley

Publishing placeWEINHEIM

Publication year2025

JournalAdvanced Materials

Journal name in sourceAdvanced Materials

Journal acronymADV MATER

Article number2502617

Volume37

Number of pages22

ISSN0935-9648

eISSN1521-4095

DOIhttps://doi.org/10.1002/adma.202502617

Web address https://doi.org/10.1002/adma.202502617

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/499520637


Abstract
Cancer-associated fibroblasts (CAFs) play a pivotal role in inducing photothermal therapy (PTT) resistance of triple-negative breast cancer (TNBC), but with unclear mechanism. Herein, aminoethyl anisamide-modified nano-biomimetic low-density lipoprotein (A-aLDL) is used to target deliver the PTT agent and artesunate (ARS) to both CAFs and cancer cells. Though CAFs are sensitive to PTT and notably transition to heat-resistant phenotype, the formed protective barrier is destroyed by ARS. Subsequently, the outstanding anti-tumor effects are achieved through PTT in multiple models with such kind of combination therapy. Interestingly, the mechanism is discovered that serine metabolism plays a major role in CAF resistance through spatially omics. ARS disrupts serine homeostasis, thereby attenuating the cascade activity of GTPases in MAPK pathway. Meanwhile, MAP2K7 is the most potential target for sensitizing PTT. By integrating ARS with PTT agents, the serine-MAPK axis in CAFs is successfully modulated, thereby overcoming PTT resistance in TNBC therapy.

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Funding information in the publication
This study was supported by the National Science Foundation (Grant No. 82372145 (H.Z.)), the Joint Fund of the Zhejiang Provincial Natural Science Foundation of China (Grant No. BD24H180004 (H.Z.)), and the grant from the Discipline Cluster of Oncology, Wenzhou Medical University, China (Grant No. z1-2023002 (H.Z.)). It was also supported by the Research Project (Grant No. 347897 (H.Z.)), Solution for Health Profile (Grant No. 336355 (H.Z.)), InFLAMES Flagship (Grant No. 337531 (H.Z.)) and Printed Intelligence Infrastructure (PII-FIRI) from Research Council of Finland. The National Natural Science Foundation of China (Grant No. 82071945, 82371978, 82311530049 (S.Z.)), Shanghai Committee of Science and Technology, China (Grant No. 21S31905400 (S.Z.)), the National Natural Science Foundation of China (Grant No. 81830058 (C.C.)), and the Shanghai Anticancer Association EYAS PROJECT (Grant No. SACA-CY22C07 (D.Z.)), China Postdoctoral Science Foundation (Grant No. 2024M760561 (D.Z.))

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Last updated on 2025-19-09 at 14:51