Evidence map›Paper›PMID 37667739›Full record

ArticleMedComm2023

Zyxin inhibits the epithelial-mesenchymal transition process in gastric cancer by upregulating SIRT1.

Jing Lou, Sha Geng, Wei He, Song-Bai Liu, Xinghong Shi, Ying Chang, Shiyuan Han, Panting Qian, Hesham M Amin, Yao-Hua Song and 2 more

Open access · goldAbstract read
In one paragraph

Article in MedComm, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Down Expression of Zyxin is Associated with Down Expression of p53 in Colorectal Cancer.International journal of molecular and cellular medicine · 2025
    Article
  5. Article
  6. Review
  7. 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

12 authors at 4 institutions in 2 countries.

Jing LouCyrus Tang Hematology Center Collaborative Innovation Center of Hematology Soochow University Suzhou China.
Sha GengCyrus Tang Hematology Center Collaborative Innovation Center of Hematology Soochow University Suzhou China.
Wei HeCyrus Tang Hematology Center Collaborative Innovation Center of Hematology Soochow University Suzhou China.
Song-Bai LiuSuzhou Key Laboratory of Medical Biotechnology Suzhou Vocational Health College Suzhou China.
Xinghong ShiCyrus Tang Hematology Center Collaborative Innovation Center of Hematology Soochow University Suzhou China.
Ying ChangCyrus Tang Hematology Center Collaborative Innovation Center of Hematology Soochow University Suzhou China.
Shiyuan HanCyrus Tang Hematology Center Collaborative Innovation Center of Hematology Soochow University Suzhou China.
Panting QianCyrus Tang Hematology Center Collaborative Innovation Center of Hematology Soochow University Suzhou China.
Hesham M AminDepartment of Hematopathology The University of Texas MD Anderson Cancer Center Houston Texas USA.
Yao-Hua SongCyrus Tang Hematology Center Collaborative Innovation Center of Hematology Soochow University Suzhou China.
Yangxin LiInstitute for Cardiovascular Science and Department of Cardiovascular Surgery First Affiliated Hospital and Medical College of Soochow University Collaborative Innovation Center of Hematology Soochow University Suzhou Jiangsu China.
Jin ZhouDepartment of General Surgery the First Affiliated Hospital of Soochow University Suzhou China.
First Affiliated Hospital of Soochow University · CNSoochow University · CNSuzhou Vocational Health College · CNThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor development relies on the stemness of cancer stem cells, which is regulated by environmental cues. Previous studies have shown that zyxin can inhibit the expression of genes for embryonic stem cell status. In the present study, the expression levels of zyxin protein in cancer tissues and adjacent noncancerous tissues from 73 gastric cancer patients with different clinical stages were analyzed by Western blot. We showed that the relative expression levels of zyxin in gastric cancer tissues (cancer tissues/adjacent tissues) were significantly downregulated in advanced clinical stages. Overexpression of zyxin inhibited the stemness and epithelial-mesenchymal transition (EMT) processes in gastric cancer cells. Zyxin also inhibited the proliferation, migration, and invasion but increased the sensitivity of cancer cells to drugs. Overexpression of zyxin in MKN45 cells inhibited tumor growth in nude mice. We show that the interactions between zyxin and SIRT1 led to the upregulation of SIRT1, reduced acetylation levels of histone H3 K9 and K23, decreased transcription levels of SNAI 1/2, and inhibition of the EMT process. This study demonstrated that zyxin negatively regulates the progression of gastric cancer by inhibiting the stemness of cancer stem cells and EMT. Our findings shed new light on the pathogenesis of gastric cancer.

Indexed as

acetylationEMT;SIRT1gastric cancerzyxin

Identifiers

PMID37667739
PMCPMC10475219
OpenAlexW4386399844

What Socratic 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 Socratic graph.