Evidence map›Paper›PMID 32227453›Full record

ArticleCancer medicine2020

Sitagliptin affects gastric cancer cells proliferation by suppressing Melanoma-associated antigen-A3 expression through Yes-associated protein inactivation.

Qi Wang, Pan Lu, Tao Wang, Qianqian Zheng, Yan Li, Sean X Leng, Xin Meng, Biao Wang, Jisheng Xie, Haiyan Zhang

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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.

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

18 citing papers in PubMed, 34 citations in OpenAlex.

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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 8 institutions in 2 countries.

Qi WangDepartment of Geriatrics, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.ORCID 0000-0003-1208-6211
Pan LuDepartment of Urinary Surgery, The Central Hospital of Xiaogan, Xiaogan, Hubei, China.
Tao WangDepartment of Pathology, Shenyang KingMed Center for Clinical Laboratory Co., Ltd., Shenyang, Liaoning, China.
Qianqian ZhengDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, Liaoning, China.
Yan LiDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Sean X LengDivision of Geriatric Medicine and Gerontology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Xin MengDepartment of Biochemistry and Molecular Biology, School of Life Sciences, China Medical University, Shenyang, Liaoning, China.
Biao WangDepartment of Biochemistry and Molecular Biology, School of Life Sciences, China Medical University, Shenyang, Liaoning, China.
Jisheng XieDepartment of Histology and Embryology, Youjiang Medical College for Nationalities, Baise, Guangxi, China.
Haiyan ZhangDepartment of Geriatrics, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
China Medical University · CNFirst Hospital of China Medical University · CNFourth Affiliated Hospital of China Medical University · CNJohns Hopkins University · USShenyang Conservatory of Music · CNShenyang Medical College · CNThe Central Hospital of Xiao gan · CNYoujiang Medical College for Nationalities · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sitagliptin is an emerging oral hypoglycemic agent that inhibits the development of a wide variety of tumors. Current researches indicate that the abnormal activation of Yes-associated protein (YAP) promotes the proliferation and poor prognosis of multiple tumors. However, the ability of sitagliptin to regulate YAP and its effects on gastric cancer (GC) cells remain unclear. Here, we first showed that sitagliptin inhibited the proliferation of GC cells, and this inhibition was regulated by Hippo pathway. Sitagliptin phosphorylated YAP in a large tumor suppressor homolog-dependent manner, thereby inhibiting YAP nuclear translocation, and promoted YAP cytoplasm retention. This inhibition can be blocked by adenosine 5'-monophosphate-activated protein kinase (AMPK). Moreover, sitagliptin could reduce the expression of tumor-testis antigen Melanoma-associated antigen-A3 through YAP. In conclusion, sitagliptin may have a potential inhibitory effect on GC by AMPK/YAP/melanoma-associated antigen-A3 pathway.

Indexed as

Cell ProliferationAdaptor Proteins, Signal TransducingAntigens, NeoplasmApoptosisBiomarkers, TumorDipeptidyl-Peptidase IV InhibitorsGene Expression Regulation, NeoplasticHumansMiddle AgedNeoplasm ProteinsPhosphorylationPrognosisSitagliptin PhosphateStomach NeoplasmsSurvival RateTranscription FactorsAdaptor Proteins, Signal TransducingAntigens, NeoplasmBiomarkers, TumorDipeptidyl-Peptidase IV InhibitorsMAGEA3 protein, humanNeoplasm ProteinsSitagliptin PhosphateTranscription FactorsYAP1 protein, humanYAP-Signaling Proteinsgastric cancerMAGE-A3sitagliptinYAP

Identifiers

PMID32227453
PMCPMC7286447
OpenAlexW3013886845

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.