Evidence map›Paper›PMID 28052030›Full record

ArticleOncotarget2017

The angiotensin II type 1 receptor antagonist telmisartan inhibits cell proliferation and tumor growth of esophageal adenocarcinoma via the AMPKα/mTOR pathway in vitro and in vivo.

Shintaro Fujihara, Asahiro Morishita, Kana Ogawa, Tomoko Tadokoro, Taiga Chiyo, Kiyohito Kato, Hideki Kobara, Hirohito Mori, Hisakazu Iwama, Tsutomu Masaki

2 registry-linked trialsOpen 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 2 registered trials, which are not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.7field-weighted citation impact, top 15% 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.

NCT06168487 phase1recruitingnot on this mapstarted 2024, after this paper: background citation

Phase I Non-Randomized, Unblinded, Single-Center Trial of Oral Telmisartan Alone or Combined With Selected Standard of Care Therapies for Prostate Cancer

TypeinterventionalSponsorTyler J CurielRan2024 to 2027Enrolled36ConditionsProstate CancerArmsTelmisartan, Standard of Care Regimen
NCT06815497 phase2recruitingnot on this mapstarted 2026, after this paper: background citation

Phase II Non-Randomized, Unblinded, Single-Center Trial of Telmisartan in Combination With Cytotoxic Regimens in Platinum-Resistant Ovarian Cancer Versus Historical Best Supportive Care

TypeinterventionalSponsorTyler J CurielRan2026 to 2029Enrolled33ConditionsOvarian CancerArmsTelmisartan
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 38 citations in OpenAlex.

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  9. The ATMolecules (Basel, Switzerland) · 2023
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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

10 authors at 1 institution in 1 country.

Shintaro FujiharaDepartment of Gastroenterology and Neurology, Kagawa University Faculty of Medicine/Graduate School of Medicine, Kagawa 761-0793, Japan.
Asahiro MorishitaDepartment of Gastroenterology and Neurology, Kagawa University Faculty of Medicine/Graduate School of Medicine, Kagawa 761-0793, Japan.
Kana OgawaDepartment of Gastroenterology and Neurology, Kagawa University Faculty of Medicine/Graduate School of Medicine, Kagawa 761-0793, Japan.
Tomoko TadokoroDepartment of Gastroenterology and Neurology, Kagawa University Faculty of Medicine/Graduate School of Medicine, Kagawa 761-0793, Japan.
Taiga ChiyoDepartment of Gastroenterology and Neurology, Kagawa University Faculty of Medicine/Graduate School of Medicine, Kagawa 761-0793, Japan.
Kiyohito KatoDepartment of Gastroenterology and Neurology, Kagawa University Faculty of Medicine/Graduate School of Medicine, Kagawa 761-0793, Japan.
Hideki KobaraDepartment of Gastroenterology and Neurology, Kagawa University Faculty of Medicine/Graduate School of Medicine, Kagawa 761-0793, Japan.
Hirohito MoriDepartment of Gastroenterology and Neurology, Kagawa University Faculty of Medicine/Graduate School of Medicine, Kagawa 761-0793, Japan.
Hisakazu IwamaLife Science Research Center, Kagawa University, Kagawa 761-0793, Japan.
Tsutomu MasakiDepartment of Gastroenterology and Neurology, Kagawa University Faculty of Medicine/Graduate School of Medicine, Kagawa 761-0793, Japan.
Kagawa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telmisartan, a widely used antihypertensive drug, is an angiotensin II type 1 (AT1) receptor blocker (ARB). This drug inhibits cancer cell proliferation, but the underlying mechanisms in various cancers, including esophageal cancer, remain unknown. The aim of the present study was to evaluate the effects of telmisartan on human esophageal cancer cell proliferation in vitro and in vivo. We assessed the effects of telmisartan on human esophageal adenocarcinoma (EAC) cells using the cell lines OE19, OE33, and SKGT-4. Telmisartan inhibited the proliferation of these three cell lines via blockade of the G0 to G1 cell cycle transition. This blockade was accompanied by a strong decrease in cyclin D1, cyclin E, and other cell cycle-related proteins. Notably, the AMP-activated protein kinase (AMPK) pathway, a fuel sensor signaling pathway, was enhanced by telmisartan. Compound C, which inhibits the two catalytic subunits of AMPK, enhanced the expression of cyclin E, leading to G0/G1 arrest in human EAC cells. In addition, telmisartan reduced the phosphorylation of epidermal growth factor receptor (p-EGFR) and ERBB2 in vitro. In our in vivo study, intraperitoneal injection of telmisartan led to a 73.2% reduction in tumor growth in mice bearing xenografts derived from OE19 cells. Furthermore, miRNA expression was significantly altered by telmisartan in vitro and in vivo. In conclusion, telmisartan suppressed human EAC cell proliferation and tumor growth by inducing cell cycle arrest via the AMPK/mTOR pathway.

Indexed as

AdenocarcinomaAMP-Activated Protein KinasesAngiotensin II Type 1 Receptor BlockersAnimalsAntineoplastic AgentsBenzimidazolesBenzoatesCell Cycle CheckpointsCell Cycle ProteinsCell Line, TumorCell ProliferationDose-Response Relationship, DrugErb-b2 Receptor Tyrosine KinasesErbB ReceptorsEsophageal NeoplasmsGene Expression Regulation, NeoplasticAMP-Activated Protein KinasesAngiotensin II Type 1 Receptor BlockersAntineoplastic AgentsBenzimidazolesBenzoatesCell Cycle ProteinsEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsMicroRNAsMTOR protein, humanTelmisartanTOR Serine-Threonine KinasesAMPKαangiotensin II type 1 receptor blockercell cycle arrestesophageal adenocarcinomatelmisartan

Identifiers

PMID28052030
PMCPMC5352420
OpenAlexW2562089821

What OpenQuestion holds

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LicenceCC BY
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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.