Evidence map›Paper›PMID 41820429›Full record

ArticleScientific reports2026

Suppression of LTBP1 enhances the sensitivity of bladder cancer to cisplatin.

Zongyang Li, Yongbo Yu, Fang Liu, Yushu Wu, Yunjiang Zang, Yanhong Ding, Zhilei Zhang

Abstract read
In one paragraph

Article in Scientific reports, 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

7 authors.

Zongyang Li *Department of Urology, West Coast Second Hospital of Qingdao University Medical Group, Qingdao, 266499, China.
Yongbo Yu *Department of Urology, The First Affiliated Hospital of Shandong Second Medical University, Weifang, 261041, China.
Fang LiuDepartment of Cardiology, The First Affiliated Hospital of Shandong Second Medical University, Weifang, 261041, China.
Yushu WuSchool of Clinical Medicine, Shandong Second Medical University, Weifang, 261041, China.
Yunjiang ZangDepartment of Urology, The First Affiliated Hospital of Shandong Second Medical University, Weifang, 261041, China.
Yanhong DingDepartment of Oncology, The First Affiliated Hospital of Shandong Second Medical University, Weifang, 261041, China. rmyydingyh@sdsmu.edu.cn.
Zhilei ZhangDepartment of Urology, The First Affiliated Hospital of Shandong Second Medical University, Weifang, 261041, China. yiyuanzhangzhilei@163.com.

Funding

Postdoctoral Innovation Program of Shandong Province SDCX-ZG-202502104Scientific Research Development Fund Project of Shandong Second Medical University Affiliated Hospital 2024FYQ022Weifang Science and Technology Development Plan Project 2024YX014
6 · The paper itself

Abstract

Cisplatin-based chemotherapy is the primary treatment for advanced bladder cancer; however, numerous patients experience treatment failure because of chemoresistance. Therefore, it is crucial to identify drivers of chemoresistance and determine strategies to counteract them to improve prognosis in bladder cancer patients. This study performed proteomics analysis of clinical samples of cisplatin-naïve and resistant bladder cancer tissues. Furthermore, the GEO and TCGA datasets were integrated, which revealed latent transforming growth factor β binding protein 1 (LTBP1) as a potential gene associated with chemoresistance in bladder cancer. LTBP1 expression was correlated with clinical stage and patient survival. LTBP1 knockdown in bladder cancer cells inhibited proliferation, migration, invasion, and chemoresistance via TGF-β-mediated epithelial-mesenchymal transition. Subcutaneous tumor and lung metastasis mouse models revealed that LTBP1 inhibition combined with cisplatin treatment significantly inhibited tumor growth and metastasis. Higher LTBP1 expression is associated with a worse prognosis and advanced stage in bladder cancer patients. In conclusion, this study revealed that LTBP1 may be a potential target for alleviating chemoresistance in bladder cancer.

Indexed as

Antineoplastic AgentsCisplatinDrug Resistance, NeoplasmLatent TGF-beta Binding ProteinsUrinary Bladder NeoplasmsAnimalsCell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansMaleMicePrognosisAntineoplastic AgentsCisplatinLatent TGF-beta Binding ProteinsLTBP1 protein, humanBladder cancerChemotherapy resistanceEMTLTBP1

Identifiers

PMID41820429
PMCPMC13106693

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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.