Evidence map›Paper›PMID 28548944›Full record

ArticleOncotarget2017

The adenosine A2b receptor promotes tumor progression of bladder urothelial carcinoma by enhancing MAPK signaling pathway.

Yihong Zhou, Xi Chu, Fei Deng, Liang Tong, Guoxiong Tong, Ye Yi, Jianye Liu, Jin Tang, Yuxin Tang, Yang Xia and 1 more

Registry-linked trialOpen access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04976660 (Phase I/II First-in-Human Study of TT-4 As a Single Agent in Participants with Advanced Selected Solid Tumors), which is not on this map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.2field-weighted citation impact, top 4% of its field
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.

NCT04976660 phase1 / phase2withdrawnnot on this mapstarted 2022, after this paper: background citation

Phase I/II First-in-Human Study of TT-4 As a Single Agent in Participants with Advanced Selected Solid Tumors

TypeinterventionalSponsorTarus Therapeutics, Inc.Ran2022 to 2023Enrolled0ConditionsColorectal Cancer, Gastric Cancer, Hepatocellular Carcinoma, Pancreatic CancerArmsTT-4
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 59 citations in OpenAlex.

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  16. Targeting purine metabolism in ovarian cancer.Journal of ovarian research · 2022
    Review
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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

11 authors at 2 institutions in 1 country.

Yihong ZhouDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Xi ChuDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Fei DengDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Liang TongDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Guoxiong TongDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Ye YiDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Jianye LiuDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Jin TangDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Yuxin TangDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Yang XiaDepartment of Biochemistry and Molecular Biology, University of Texas Medical School, Houston, Texas, USA.
Yingbo DaiDepartment of Urology, The Third Xiangya Hospital of Central South University, Changsha, China.
Central South University · CNThird Xiangya Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The adenosine A2b receptor (A2bR) was considered to play an oncogenic role in many human malignancies. However, the expression and molecular function of A2bR in bladder urothelial carcinoma (BUC) have not been well elucidated. Herein, we found that the expression of A2bR was higher than other adenosine receptors in BUC tissues and cells, and it was upregulated in BUC tissues compared with matched normal bladder tissues. Furthermore, high expression of A2bR was associated with poor prognosis of patients with BUC. In addition, suppression of A2bR inhibited the proliferation, migration and invasion of BUC cells and arrested the cell cycle at the G1 phase. Finally, we demonstrated that downregulation of A2bR inhibited the proliferation, migration and invasion of BUC in part via the MAPK signaling pathway, increasing the levels of P21 but decreasing the levels of cyclin B1, D, E1, MMP-2 and MMP-9. Overexpression of MMP-2 could rescue BUC cells migration and invasion. Thus, the present study indicates that A2bR may play a potential oncogenic role in BUC progression and act as a potential biomarker to identify BUC patients with poor clinical outcomes.

Indexed as

MAP Kinase Signaling SystemAdultAgedAnimalsBiomarkersCell Line, TumorCell MovementCell ProliferationDisease Models, AnimalDisease ProgressionFemaleG1 Phase Cell Cycle CheckpointsGene ExpressionGene Knockdown TechniquesHumansKaplan-Meier EstimateBiomarkersMatrix Metalloproteinase 2Matrix Metalloproteinase 9Receptor, Adenosine A2Badenosine A2b receptorbladder urothelial carcinomaMAPK signalingprognosis

Identifiers

PMID28548944
PMCPMC5564722
OpenAlexW2612146974

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.