Evidence map›Paper›PMID 28869796›Full record

ArticleCancer science2017

Antitumor effects of eribulin depend on modulation of the tumor microenvironment by vascular remodeling in mouse models.

Ken Ito, Shusei Hamamichi, Takanori Abe, Tsuyoshi Akagi, Hiroshi Shirota, Satoshi Kawano, Makoto Asano, Osamu Asano, Akira Yokoi, Junji Matsui and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Cancer science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05965141 (A Phase II Prospective Single-arm Clinical Study of Aribulin Combined With Carboplatin and Bevacizumab in the First-line Treatment of Platinum-sensitive Recurrent Ovarian Cancer), which is not on this map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.7field-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.

NCT05965141 phase1 / phase2unknown statusnot on this mapstarted 2023, after this paper: background citation

A Phase II Prospective Single-arm Clinical Study of Aribulin Combined With Carboplatin and Bevacizumab in the First-line Treatment of Platinum-sensitive Recurrent Ovarian Cancer

TypeinterventionalSponsorSecond Affiliated Hospital of Guangzhou Medical UniversityRan2023 to 2025Enrolled38ConditionsOvarian CancerArmsAribulin, carboplatin, bevacizumab
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 68 citations in OpenAlex.

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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 2 institutions in 1 country.

Ken ItoHalichondrin Research Laboratory, Eisai Co., Ltd, Tsukuba, Japan.ORCID http://orcid.org/0000-0002-6997-4271
Shusei HamamichiDivision of Functional Imaging, National Cancer Center, Kashiwa, Japan.
Takanori AbeHalichondrin Research Laboratory, Eisai Co., Ltd, Tsukuba, Japan.
Tsuyoshi AkagiHalichondrin Research Laboratory, Eisai Co., Ltd, Tsukuba, Japan.
Hiroshi ShirotaHalichondrin Research Laboratory, Eisai Co., Ltd, Tsukuba, Japan.
Satoshi KawanoHalichondrin Research Laboratory, Eisai Co., Ltd, Tsukuba, Japan.
Makoto AsanoBiology Research, Oncology, Eisai Co., Ltd., Tsukuba, Japan.
Osamu AsanoHalichondrin Research Laboratory, Eisai Co., Ltd, Tsukuba, Japan.
Akira YokoiHalichondrin Research Laboratory, Eisai Co., Ltd, Tsukuba, Japan.
Junji MatsuiBiology Research, Oncology, Eisai Co., Ltd., Tsukuba, Japan.
Izumi O UmedaDivision of Functional Imaging, National Cancer Center, Kashiwa, Japan.
Hirofumi FujiiDivision of Functional Imaging, National Cancer Center, Kashiwa, Japan.
Eisai (Japan) · JPNational Cancer Center Hospital East · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously reported that eribulin mesylate (eribulin), a tubulin-binding drug (TBD), could remodel tumor vasculature (i.e. increase tumor vessels and perfusion) in human breast cancer xenograft models. However, the role of this vascular remodeling in antitumor effects is not fully understood. Here, we investigated the effects of eribulin-induced vascular remodeling on antitumor activities in multiple human cancer xenograft models. Microvessel densities (MVD) were evaluated by immunohistochemistry (CD31 staining), and antitumor effects were examined in 10 human cancer xenograft models. Eribulin significantly increased MVD compared to the controls in six out of 10 models with a correlation between enhanced MVD levels and antitumor effects (R

Indexed as

AnimalsDoxorubicinFemaleFuransHCT116 CellsHumansKetonesMiceNeoplasmsPolyether PolyketidesPolyethylene GlycolsTumor MicroenvironmentVascular RemodelingXenograft Model Antitumor AssaysDoxorubicineribulinFuransKetonesliposomal doxorubicinPolyether PolyketidesPolyethylene GlycolsEribulinliposomenatural killer celltubulin dynamics inhibitorvascular remodeling

Identifiers

PMID28869796
PMCPMC5665763
OpenAlexW2753016107

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.