Evidence map›Paper›PMID 42596501›Full record

ArticleAdvanced healthcare materials2026

Overcoming Photodynamic Therapy Resistance: GSH-Responsive AIE Photosensitizer-Hydroxycamptothecin Nanoliposomes for Extrahepatic Cholangiocarcinoma.

Yong Qu, Tao Peng, Yating Zhang, Juanmei Cao, Birong Wang, Chuxing Chai, Zhiyuan Gao, Yiting Xu, Yifan Jin, Yuqing Wang and 10 more

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Yong QuDepartment of Hepatobiliary Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Tao PengDepartment of Hepatobiliary Surgery, The First People's Hospital of Jingzhou, The First Affiliated Hospital of Yangtze University, Jingzhou, China.ORCID https://orcid.org/0000-0002-5779-3377
Yating ZhangDepartment of Hepatobiliary Surgery, Division of Life Sciences and Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, China.
Juanmei CaoDepartment of Dermatology, The First Affiliated Hospital of Shihezi University, Shihezi, China.ORCID https://orcid.org/0000-0002-6077-2585
Birong WangDepartment of Thyroid Gland and Breast Surgery, Wuhan Fourth Hospital, Wuhan, China.
Chuxing ChaiDepartment of Hepatobiliary Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Zhiyuan GaoFrontiers Science Center For Cell Responses, State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, and College of Life Sciences, Ministry of Education, Nankai University, Tianjin, China.
Yiting XuCentral Laboratory, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yifan JinHospital For Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, China.ORCID https://orcid.org/0000-0002-5250-5049
Yuqing WangDepartment of Clinical Nutrition, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0000-0001-9320-3517
Zhuoxia LiDepartment of Hepatobiliary Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Xu LiuDepartment of Hepatobiliary Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Tianqi ZhaoDepartment of Dermatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yufan ChenDepartment of Dermatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0009-0009-6002-0699
Weimin LvDepartment of Hepatobiliary Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Di LuDepartment of Dermatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Changzheng HuangDepartment of Dermatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0000-0003-1531-1269
Dan DingFrontiers Science Center For Cell Responses, State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, and College of Life Sciences, Ministry of Education, Nankai University, Tianjin, China.ORCID https://orcid.org/0000-0003-1873-6510
Jinxiang ZhangDepartment of Emergency Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0000-0002-5447-272X
Min LiDepartment of Hepatobiliary Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0000-0002-0047-2804

Funding

Doctoral Scientific Research Fund of The First Affiliated Hospital of Yangtze University 2022DIF05Hebei Natural Science Foundation B2025110067National Natural Science Foundation of China 82172754the Joint Fund Project of Hubei Provincial Natural Science Foundation 2026AFC0601Yangtze University Health Science Center, Yangtze University Medical Innovation Fund 2022MIF07
6 · The paper itself

Abstract

Photodynamic therapy (PDT) has been shown to improve survival and quality of life in patients with unresectable extrahepatic cholangiocarcinoma. However, its therapeutic efficacy is frequently limited by the survival of residual tumor cells that can re-enter the proliferative cycle. Our previous studies showed that residual cholangiocarcinoma cells can re-enter the proliferative cycle following PDT accompanied by hypoxia-induced activation of the HIF-1α survival pathway and intracellular antioxidant programs. To address this residual viability, we developed a glutathione-responsive targeted nanosystem (TSH NPs), in which the aggregation-induced emission (AIE) photosensitizer TPA-Ph-RDN is conjugated to the chemotherapeutic agent hydroxycamptothecin (HCPT) via a disulfide linkage. This design enables HCPT to exert direct cytotoxic effects while simultaneously suppressing the HIF-1α-mediated hypoxic adaptation pathway, thereby reducing residual tumor viability and enhancing PDT efficacy. This strategy achieves a dual-mechanism, two-pronged therapeutic effect. Both in vitro and in vivo studies demonstrated that TSH NPs elicited markedly synergistic antitumor activity, highlighting their potential as a promising therapeutic approach for improving clinical outcomes in patients with eCCA.

Indexed as

Bile Duct NeoplasmsCamptothecinCholangiocarcinomaGlutathioneLiposomesNanoparticlesPhotochemotherapyPhotosensitizing AgentsAnimalsCell Line, TumorHumansMiceMice, NudeXenograft Model Antitumor AssaysCamptothecinGlutathionehydroxycamptothecinumLiposomesPhotosensitizing Agentsaggregation‐induced emissionchemotherapyextrahepatic cholangiocarcinomahydroxycamptothecinphotodynamic therapy

Identifiers

PMID42596501
PMCPMC13586644

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.