Evidence map›Paper›PMID 37250161›Full record

ReviewActa pharmaceutica Sinica. B2023

The hippo kinases MST1/2 in cardiovascular and metabolic diseases: A promising therapeutic target option for pharmacotherapy.

Yunfei Yin, Mingyue Tan, Lianhua Han, Lei Zhang, Yue Zhang, Jun Zhang, Wanqian Pan, Jiaxiang Bai, Tingbo Jiang, Hongxia Li

Open access · diamondAbstract readReview
In one paragraph

Review in Acta pharmaceutica Sinica. B, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 17 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 2 institutions in 1 country.

Yunfei YinDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Mingyue TanDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Lianhua HanDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Lei ZhangDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Yue ZhangDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Jun ZhangDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Wanqian PanDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Jiaxiang BaiDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Tingbo JiangDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Hongxia LiDepartment of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Soochow University · CNUniversity of Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular diseases (CVDs) and metabolic disorders are major components of noncommunicable diseases, causing an enormous health and economic burden worldwide. There are common risk factors and developmental mechanisms among them, indicating the far-reaching significance in exploring the corresponding therapeutic targets. MST1/2 kinases are well-established proapoptotic effectors that also bidirectionally regulate autophagic activity. Recent studies have demonstrated that MST1/2 influence the outcome of cardiovascular and metabolic diseases by regulating immune inflammation. In addition, drug development against them is in full swing. In this review, we mainly describe the roles and mechanisms of MST1/2 in apoptosis and autophagy in cardiovascular and metabolic events as well as emphasis on the existing evidence for their involvement in immune inflammation. Moreover, we summarize the latest progress of pharmacotherapy targeting MST1/2 and propose a new mode of drug combination therapy, which may be beneficial to seek more effective strategies to prevent and treat CVDs and metabolic disorders.

Indexed as

ApoptosisAutophagyCardiovascular diseasesImmuneMetabolic diseasesMST1/2 kinasesRegulationTherapy

Identifiers

PMID37250161
PMCPMC10213817
OpenAlexW4319159030

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.