Evidence map›Paper›PMID 36717701›Full record

ArticleOncogene2023

E-cadherin is a biomarker for ferroptosis sensitivity in diffuse gastric cancer.

Alexander M Minikes, Yu Song, Yan Feng, Changhwan Yoon, Sam S Yoon, Xuejun Jiang

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Oncogene, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  10. ESRP1 exerts anti-tumor role by promoting ferroptosis in diffuse-type gastric cancer.Journal of experimental & clinical cancer research : CR · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 2 countries.

Alexander M MinikesCell Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Yu SongCell Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA. sy5449@163.com.
Yan FengCell Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Changhwan YoonDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Sam S YoonDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Xuejun JiangCell Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA. jiangx@mskcc.org.ORCID http://orcid.org/0000-0002-8670-3828
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Ferroptosis, Cellular Metabolism, and CancerR01CA204232 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JIANG, XUEJUN · 2017 to 2025
$4.1M
Ferroptosis and Cancer Cell SignalingR01CA258622 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Xuejun Jiang · 2022 to 2026
$2.2M
Cell adhesion and ferroptosis: investigating a potential vulnerability in cancer cellsF31CA247112 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MINIKES, ALEXANDER MICHAEL · 2020 to 2021
$92k
NCI NIH HHS F31 CA247112NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA204232NCI NIH HHS R01 CA258622
6 · The paper itself

Abstract

Gastric cancer is the third most common cause of cancer-related death worldwide. Diffuse-type gastric cancer (DGC) is a particularly aggressive subtype that is both difficult to detect and treat. DGC is distinguished by weak cell-cell cohesion, most often due to loss of the cell adhesion protein E-cadherin, a common occurrence in highly invasive, metastatic cancer cells. In this study, we demonstrate that loss-of-function mutation of E-cadherin in DGC cells results in their increased sensitivity to the non-apoptotic, iron-dependent form of cell death, ferroptosis. Homophilic contacts between E-cadherin molecules on adjacent cells suppress ferroptosis through activation of the Hippo pathway. Furthermore, single nucleotide mutations observed in DGC patients that ablate the homophilic binding capacity of E-cadherin reverse the ability of E-cadherin to suppress ferroptosis in both cell culture and xenograft models. Importantly, although E-cadherin loss in cancer cells is considered an essential event for epithelial-mesenchymal transition and subsequent metastasis, we found that circulating DGC cells lacking E-cadherin expression possess lower metastatic ability, due to their increased susceptibility to ferroptosis. Together, this study suggests that E-cadherin is a biomarker predicting the sensitivity to ferroptosis of DGC cells, both in primary tumor tissue and in circulation, thus guiding the usage of future ferroptosis-inducing therapeutics for the treatment of DGC.

Indexed as

FerroptosisStomach NeoplasmsBiomarkersCadherinsHumansMutationBiomarkersCadherins

Identifiers

PMID36717701
PMCPMC10291936
OpenAlexW4318480842

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.