Evidence map›Paper›PMID 35982907›Full record

ArticleInternational journal of biological sciences2022

Role of PCK2 in the proliferation of vascular smooth muscle cells in neointimal hyperplasia.

Dai Sik Ko, Junho Kang, Hye Jin Heo, Eun Kyoung Kim, Kihun Kim, Jin Mo Kang, YunJae Jung, Seung Eun Baek, Yun Hak Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Elesclomol-Induced Copper Influx Attenuates Lung Adenocarcinoma Progression With Involvement of the ER Stress/PCK2 Axis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
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

9 authors at 4 institutions in 1 country.

Dai Sik KoDivision of Vascular Surgery, Department of General Surgery, Gachon University Gil Medical Center, Incheon, Republic of Korea.
Junho KangMedical Research Institute, Pusan National University, Busan, Republic of Korea.
Hye Jin HeoDepartment of Anatomy, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Eun Kyoung KimDepartment of Anatomy, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Kihun KimDepartment of Occupational and Environmental Medicine, Kosin University Gospel Hospital, Republic of Korea.
Jin Mo KangDivision of Vascular Surgery, Department of General Surgery, Gachon University Gil Medical Center, Incheon, Republic of Korea.
YunJae JungDepartment of Microbiology, College of Medicine, Gachon University, Incheon, Republic of Korea.
Seung Eun BaekDepartment of Anatomy, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Yun Hak KimDepartment of Anatomy, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
Pusan National University · KRGachon University Gil Medical Center · KRGachon University · KRKosin University Gospel Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular smooth muscle cell (VSMC) proliferation is a hallmark of neointimal hyperplasia (NIH) in atherosclerosis and restenosis post-balloon angioplasty and stent insertion. Although numerous cytotoxic and cytostatic therapeutics have been developed to reduce NIH, it is improbable that a multifactorial disease can be successfully treated by focusing on a preconceived hypothesis. We, therefore, aimed to identify key molecules involved in NIH via a hypothesis-free approach. We analyzed four datasets (GSE28829, GSE43292, GSE100927, and GSE120521), evaluated differentially expressed genes (DEGs) in wire-injured femoral arteries of mice, and determined their association with VSMC proliferation

Indexed as

AtherosclerosisPhosphoenolpyruvate Carboxykinase (ATP)Plaque, AtheroscleroticAnimalsCell MovementCell ProliferationCells, CulturedDisease Models, AnimalHumansHyperplasiaMiceMice, Inbred C57BLMice, KnockoutMuscle, Smooth, VascularMyocytes, Smooth MuscleNeointimaPCK2 protein, humanPhosphoenolpyruvate Carboxykinase (ATP)Proto-Oncogene Proteins c-aktRNA, Small InterferingAkt-FoxO-PCK2 pathwayatherosclerosisneointimal hyperplasiaPCK2vascular smooth muscle cell proliferation

Identifiers

PMID35982907
PMCPMC9379418
OpenAlexW4291130689

What OpenQuestion holds

Textmetadata
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.