Evidence map›Paper›PMID 39399655›Full record

ArticleInternational journal of clinical and experimental pathology2024

STAT1 as a potential therapeutic target to treat bladder cancer.

Qin Zhang, Shi Fu, Xiaotao Li, Haifeng Wang, Jiansong Wang

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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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

5 authors.

Qin ZhangDepartment of Gynaecology, The Second Affiliated Hospital of Kunming Medical University Kunming 650101, Yunnan, China.
Shi FuDepartment of Gynaecology, The Second Affiliated Hospital of Kunming Medical University Kunming 650101, Yunnan, China.
Xiaotao LiDepartment of Andriatrics, The Second Affiliated Hospital of Kunming Medical University Kunming 650101, Yunnan, China.
Haifeng WangDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, Yunnan Institute of Urology Kunming 650101, Yunnan, China.
Jiansong WangDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, Yunnan Institute of Urology Kunming 650101, Yunnan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies have reported that STAT1 (Signal Transducer and Activator of Transcription 1) is associated with multiple tumor progression. This study aimed to investigate the role and related mechanisms of STAT1 in bladder cancer.

methodsSTAT1 expression in bladder cancer tissues and human bladder cancer cell lines was assessed by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The bladder cancer cell line T24 was transfected with overexpressing lentivirus targeting STAT1. Cell proliferation, invasion, and apoptosis were measured by Cell Counting Kit-8, Transwell assays, and flow cytometric analysis. Furthermore, RNA-Seq was performed to identify the downstream signaling pathways. Finally, the signaling pathway-related molecules were determined by RT-qPCR and western blot assays.

resultsThe overexpression of STAT1 inhibited bladder cancer cell proliferation and invasion while enhancing apoptosis. Moreover, the overexpression of STAT1 in bladder cancer cells delayed tumor tumorigenesis in vitro. Mechanistically, RNA-Seq analysis revealed that the JAK-STAT signaling pathway was up-regulated, especially SOCS1 (suppressor of cytokine signaling 1) and SOCS3 (suppressor of cytokine signaling 3) in STAT1-sufficient cells.

conclusionsThese results indicate the potential of STAT1 as a therapeutic target in bladder cancer.

Indexed as

Bladder cancerpathogenesisSOCS1SOCS3STAT1

Identifiers

PMID39399655
PMCPMC11470427

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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.