Evidence map›Paper›PMID 29510160›Full record

ArticleMechanisms of ageing and development2018

Tropomyosin 2 heterozygous knockout in mice using CRISPR-Cas9 system displays the inhibition of injury-induced epithelial-mesenchymal transition, and lens opacity.

Teppei Shibata, Shinsuke Shibata, Yasuhito Ishigaki, Etsuko Kiyokawa, Masahito Ikawa, Dhirendra P Singh, Hiroshi Sasaki, Eri Kubo

Open access · greenAbstract read
In one paragraph

Article in Mechanisms of ageing and development, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Characterization of Alternative Splicing in High-Risk Wilms' Tumors.International journal of molecular sciences · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Drebrin, an actin-binding protein, is required for lens morphogenesis and growth.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Article
  8. Article
  9. EMT signaling: potential contribution of CRISPR/Cas gene editing.Cellular and molecular life sciences : CMLS · 2020
    Review
  10. Video recording and light intensity change analysis during cataract surgery using an animal model.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2019
    Article
  11. Review
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

8 authors at 4 institutions in 2 countries.

Teppei ShibataDepartment of Ophthalmology, Kanazawa Medical University, Ishikawa, Japan.
Shinsuke ShibataDepartment of Ophthalmology, Kanazawa Medical University, Ishikawa, Japan.
Yasuhito IshigakiMedical Research Institute, Kanazawa Medical University, Ishikawa, Japan.
Etsuko KiyokawaDepartment of Oncogenic Pathology, Kanazawa Medical University, Ishikawa, Japan.
Masahito IkawaResearch Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Dhirendra P SinghDepartment of Ophthalmology and Visual Sciences, University of Nebraska Medical Center, Omaha, NE, USA.
Hiroshi SasakiDepartment of Ophthalmology, Kanazawa Medical University, Ishikawa, Japan.
Eri KuboDepartment of Ophthalmology, Kanazawa Medical University, Ishikawa, Japan. Electronic address: kuboe@kanazawa-med.ac.jp.
Kanazawa Medical University · JPKanazawa University · JPThe University of Osaka · JPUniversity of Nebraska Medical Center · US

Funding

Regulation and Function of Prdx6 in eye lens during Aging & Oxidative StressR01EY024589 · NEI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SINGH, DHIRENDRA P · 2014 to 2018
$1.9M
NEI NIH HHS R01 EY024589
6 · The paper itself

Abstract

The process of epithelial-mesenchymal transition (EMT) of lens epithelial cells (LECs) after cataract surgery contributes to tissue fibrosis, wound healing and lens regeneration via a mechanism not yet fully understood. Here, we show that tropomyosin 2 (Tpm2) plays a critical role in wound healing and lens aging. Posterior capsular opacification (PCO) after lens extraction surgery was accompanied by elevated expression of Tpm2. Tpm2 heterozygous knockout mice, generated via the clustered regularly interspaced short palindromic repeat/Cas9 (CRISPR/Cas9) system showed promoted progression of cataract with age. Further, injury-induced EMT of the mouse lens epithelium, as evaluated histologically and by the expression patterns of Tpm1 and Tpm2, was attenuated in the absence of Tpm2. In conclusion, Tpm2 may be important in maintaining lens physiology and morphology. However, Tpm2 is involved in the progression of EMT during the wound healing process of mouse LECs, suggesting that inhibition of Tpm2 may suppress PCO.

Indexed as

AgingCataractCRISPR-Cas SystemsGene Knockdown TechniquesLens, CrystallineAnimalsEpithelial-Mesenchymal TransitionFemaleMiceMice, KnockoutTropomyosinWound HealingTropomyosinCataractEpithelial-mesenchymal transitionLensPosterior capsular opacificationTropomyosin

Identifiers

PMID29510160
PMCPMC6013838
OpenAlexW2791342801

What OpenQuestion holds

Textmetadata
LicenceTDM
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.