Evidence map›Paper›PMID 38258402›Full record

ArticleThoracic cancer2024

Implication of IZUMO2 in the cell-in-cell phenomenon: A potential therapeutic target for triple-negative breast cancer.

Toshiya Higashi, Chiemi Saigo, Wakana Chikaishi, Hirokatsu Hayashi, Yuki Hanamatsu, Manabu Futamura, Nobuhisa Matsuhashi, Tamotsu Takeuchi

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

8 authors at 2 institutions in 1 country.

Toshiya HigashiDepartment of Gastroenterological Surgery and Pediatric Surgery, Gifu University Graduate School of Medicine, Gifu, Japan.
Chiemi SaigoDepartment of Pathology and Translational Research, Gifu University Graduate School of Medicine, Gifu, Japan.ORCID 0000-0002-1537-0093
Wakana ChikaishiDepartment of Gastroenterological Surgery and Pediatric Surgery, Gifu University Graduate School of Medicine, Gifu, Japan.
Hirokatsu HayashiDepartment of Gastroenterological Surgery and Pediatric Surgery, Gifu University Graduate School of Medicine, Gifu, Japan.
Yuki HanamatsuDepartment of Pathology and Translational Research, Gifu University Graduate School of Medicine, Gifu, Japan.ORCID 0000-0003-0181-1334
Manabu FutamuraDepartment of Breast Surgery, Gifu University Hospital, Gifu, Japan.
Nobuhisa MatsuhashiDepartment of Gastroenterological Surgery and Pediatric Surgery, Gifu University Graduate School of Medicine, Gifu, Japan.
Tamotsu TakeuchiDepartment of Pathology and Translational Research, Gifu University Graduate School of Medicine, Gifu, Japan.ORCID 0000-0002-4264-3632
Gifu University · JPGifu University Hospital · JP

Funding

Kaken 23K06423
6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) is characterized by the loss of estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2. The aggressive clinicopathological features and resistance to currently available therapeutics of the disease warrant an urgent need for the development of novel alternate therapeutic options. We have previously reported adiponectin-expressing regulatory T cells (A-Tregs), which can induce apoptosis in TNBC through the cell-in-cell phenomenon. In this study, we aimed to elucidate the molecule that allows TNBC cells to engulf A-Tregs.

methodsA monoclonal antibody, which repressed the engulfment of A-Tregs by TNBC cells, was developed. Immunoprecipitation followed by mass spectrometry and small interfering RNAs-mediated gene silencing was performed to characterize the antigen.

resultsWe successfully generated a monoclonal antibody, designated G1D7, which abrogated the engulfment of A-Tregs by TNBC and subsequent A-Treg-mediated apoptosis. G1D7 detected the immunoglobulin-like type I membrane protein IZUMO2, a molecule related to IZUMO1 that is essential for cell-cell membrane binding and fusion of sperm to oocyte.

conclusionThe findings highlight the importance of IZUMO2 on TNBC cells in facilitating the cell-in-cell phenomenon by A-Tregs.

Indexed as

Triple Negative Breast NeoplasmsAntibodies, MonoclonalApoptosisCell Line, TumorCell ProliferationHumansMaleReceptors, EstrogenSemenAntibodies, MonoclonalReceptors, Estrogenadiponectin-expressing Tregscell-in-cell activityIZUMO2monoclonal antibodytriple-negative breast cancer

Identifiers

PMID38258402
PMCPMC10912533
OpenAlexW4391142360

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.