Evidence map›Paper›PMID 40212294›Full record

ArticleSmall science2023

Targeting PD-L1 with DNA Aptamers and Conjugated with Gemcitabine as a Novel Therapeutic Strategy for Bladder Cancer Chemotherapy Combined with Immunotherapy.

Xing Hu, Hongliang Zeng, Yongbo Peng, Minhua Deng, Wei Xiang, Biao Liu, Jiahao Liu, Yunlong Fu, Zhiqiang Hu, Weibin Hou and 5 more

Abstract read
In one paragraph

Article in Small science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Aptamers in Drug Delivery Development.Materials today (Kidlington, England) · 2025
    Article
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

15 authors.

Xing HuDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Hongliang ZengCenter of Medical Laboratory Animal Hunan Academy of Chinese Medicine Changsha Hunan 410013 China.
Yongbo PengChongqing Key Laboratory for Pharmaceutical Metabolism Research College of Pharmacy Chongqing Medical University No.1, Yixueyuan Road Chongqing 400016 China.
Minhua DengDepartment of Urology Sun Yat-sen University Cancer Center No. 651, Dongfeng Road East Guangzhou Guangdong 510060 China.
Wei XiangDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Biao LiuDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Jiahao LiuDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Yunlong FuDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Zhiqiang HuDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Weibin HouDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Xuewen LiuDepartment of Oncology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Jin TangDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Zhi LongDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Long WangDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.
Jianye LiuDepartment of Urology The Third Xiangya Hospital of Central South University No.138, Tongzipo Road Changsha Hunan 410013 China.ORCID 0000-0002-7953-3672

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to the poor stability and adverse effects of chemotherapy drugs, such as gemcitabine, the current effectiveness of traditional chemotherapy is minimal. Some patients also show a low response rate to immunotherapy. Therefore, a novel material PD-L1-GEMs is designed and synthesized with targeted specificity. PD-L1-GEMs specifically bind to bladder cancer cells. Free gemcitabine cleaved by a phosphatase enters bladder cancer cells through the macropinocytosis pathway and induces cytotoxicity. PD-L1-GEMs show good stability, binding specificity, and significant inhibitory effects in vitro. Two bladder tumor models (subcutaneous model and in situ model) show inhibition of growth and progression in PD-L1-GEMs treatment, as well as good biosafety in vivo. The PD-L1 aptamer blocks the binding of PD-L1 on the tumor cell surface to PD-1 on T lymphocytes, restoring their immune function, inducing cytokine production and aggregation, and exerting an immune killing role on bladder cancer cells. PD-L1-GEMs represent a successful chemotherapy-immunotherapy strategy for bladder cancer.

Indexed as

bladder cancerchemotherapyimmunotherapyPD-L1 aptamerstargeted therapy

Identifiers

PMID40212294
PMCPMC11936014

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.