Evidence map›Paper›PMID 41986462›Full record

ArticleScientific reports2026

Therapeutic potential of asparagus polysaccharide in bladder cancer treatment via modulation of PI3K/AKT/mTOR signaling.

Jinguo Wang, Haolin Liu, Kai Li, Ziping Xie

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.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jinguo Wang *Department of Andrology, Shiyan Renmin Hospital, Shiyan, 442000, Hubei, China.
Haolin Liu *Department of Pathology, Shiyan Renmin Hospital, Shiyan, 442000, Hubei, China.
Kai LiDepartment of Pathology, Shiyan Renmin Hospital, Shiyan, 442000, Hubei, China. 13593752880@163.com.
Ziping XieDepartment of Andrology, Shiyan Renmin Hospital, Shiyan, 442000, Hubei, China. 12559564@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Bladder cancer (BCa) is one of the most prevalent malignant tumors worldwide, with high incidence and recurrence rates, underscoring the urgent need for safe and effective therapeutic strategies. Recently, asparagus polysaccharide (ASP) has attracted attention for its diverse bioactivities, including anticancer, anti-inflammatory, and low-toxicity properties. However, its effects on BCa remain poorly understood. Objective This study aims to investigate the effects of ASP on bladder cancer cells and to elucidate the underlying molecular mechanisms. Methods The effects of ASP on T24 and 5637 bladder cancer cells were assessed using the cell counting Kit-8 (CCK-8), colony formation, wound healing, transwell invasion, TUNEL, and ROS assays. Western blot analysis was performed to assess apoptosis-related proteins (Bax, cleaved Caspase-3, Bcl-2) and key proteins of the PI3K/AKT/mTOR pathway. Additionally, IGF-1, a pathway activator, was used to explore ASP's mechanistic effects. Results ASP inhibited cell proliferation, migration, and invasion in a dose-dependent manner, and also induced apoptosis and elevated ROS levels. Western blot analysis revealed ASP-mediated downregulation of PI3K/AKT/mTOR signaling, as evidenced by reduced phosphorylation of PI3K, AKT, and mTOR. Co-treatment with IGF-1 partially reversed these effects, restoring phosphorylation of PI3K/AKT/mTOR components and cellular migration and invasion, indicating ASP's anticancer activity was mediated through this pathway. Conclusion ASP exerted anticancer effects in BCa by inhibiting PI3K/AKT/mTOR pathway, suppressing proliferation and invasion, and inducing apoptosis. These findings underscore ASP's potential as a novel therapeutic agent for bladder cancer treatment.

Indexed as

Asparagus PlantPhosphatidylinositol 3-KinasesPolysaccharidesProto-Oncogene Proteins c-aktSignal TransductionTOR Serine-Threonine KinasesUrinary Bladder NeoplasmsApoptosisCell Line, TumorCell MovementCell ProliferationHumansMTOR protein, humanPhosphatidylinositol 3-KinasesPolysaccharidesProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesAsparagus polysaccharideBladder cancerPI3K/AKT/mTOR pathway

Identifiers

PMID41986462
PMCPMC13243540

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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.