Evidence map›Paper›PMID 37261089›Full record

ArticleOncoimmunology2023

Eribulin mesylate exerts antitumor effects via CD103.

Kazumasa Oya, Yoshiyuki Nakamura, Rei Watanabe, Ryota Tanaka, Yuki Ichimura, Noriko Kubota, Yutaka Matsumura, Hideaki Tahara, Naoko Okiyama, Manabu Fujimoto and 2 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Identification of proliferating CD103Virchows Archiv : an international journal of pathology · 2026
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  2. Article
  3. 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 1 country.

Kazumasa OyaThe Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Yoshiyuki NakamuraThe Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Rei WatanabeThe Department of Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan.
Ryota TanakaThe Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Yuki IchimuraThe Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Noriko KubotaThe Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Yutaka MatsumuraThe Department of Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan.
Hideaki TaharaProject Division of Cancer Biomolecular Therapy, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Naoko OkiyamaDepartment of Dermatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Manabu FujimotoThe Department of Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan.
Toshifumi NomuraThe Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Yasuhiro FujisawaThe Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
University of Tsukuba · JPOsaka University · JPOsaka Medical Center for Cancer and Cardiovascular Diseases · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eribulin mesylate (ERB) is a synthetic analog of halichondrin B, inhibiting tumor cell growth by disrupting microtubule function. Recently, anticancer drugs have been shown to not only act directly on tumor cells but also to exert antitumor effects by modifying the tumor environment. Although ERB has also been speculated to modify the tumor microenvironment including the immune response to tumors, the precise mechanism remains unclear. In our study, ERB suppressed the tumor growth of MC38 colon cancer in wildtype mice, whereas ERB failed to inhibit the tumor growth in Rag1-deficient mice which lack both B and T cells. Moreover, depletion of either CD4

Indexed as

Antineoplastic AgentsNeoplasmsAnimalsCadherinsCD8-Positive T-LymphocytesFuransKetonesLymphocyte ActivationMicePolyether PolyketidesPrognosisTumor MicroenvironmentAntineoplastic AgentsCadherinseribulinFuransKetonesPolyether Polyketidesantitumor effectCD103eribulin mesylateimmune checkpointresident memory T cells

Identifiers

PMID37261089
PMCPMC10228394
OpenAlexW4378627997

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.