Evidence map›Paper›PMID 38849479›Full record

ArticleBritish journal of cancer2024

Synthetic retinoid-mediated preconditioning of cancer-associated fibroblasts and macrophages improves cancer response to immune checkpoint blockade.

Takayuki Owaki, Tadashi Iida, Yuki Miyai, Katsuhiro Kato, Tetsunari Hase, Makoto Ishii, Ryota Ando, Kunihiko Hinohara, Tomohiro Akashi, Yasuyuki Mizutani and 17 more

Registry-linked trialAbstract read
In one paragraph

Article in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06983210 (Multi-center, Open-Label, Single Arm Trial for Evaluation of the Efficacy and Safety in the First Line Combination Therapy of Gemcitabine, Cisplatin and Nivolumab With Additional Pretreatment of AM80 for Urothelial Carcinoma Patients), which is not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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.

NCT06983210 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

Multi-center, Open-Label, Single Arm Trial for Evaluation of the Efficacy and Safety in the First Line Combination Therapy of Gemcitabine, Cisplatin and Nivolumab With Additional Pretreatment of AM80 for Urothelial Carcinoma Patients

TypeinterventionalSponsorNagoya UniversityRan2025 to 2029Enrolled43ConditionsUrothelial Carcinoma Bladder, Urothelial Carcinoma of the Renal Pelvis and Ureter, Urothelial Carcinoma Urethra, Urothelial Carcinoma RecurrentArmsAdd-on effect of adding tamivarotene (AM80) to gemcitabine, cisplatin, and nivolumab combination therapy
3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

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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

27 authors.

Takayuki Owaki *Department of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Tadashi Iida *Department of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan. iidatyuw@med.nagoya-u.ac.jp.ORCID http://orcid.org/0000-0001-5491-6012
Yuki MiyaiDepartment of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Katsuhiro KatoDepartment of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0002-9710-1451
Tetsunari HaseDepartment of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0002-9653-8424
Makoto IshiiDepartment of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0003-4396-1664
Ryota AndoDepartment of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kunihiko HinoharaDepartment of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Tomohiro AkashiDivision of Systems Biology, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Yasuyuki MizutaniDepartment of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Takuya IshikawaDepartment of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Shinji MiiDepartment of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0001-8266-3235
Yukihiro ShirakiDepartment of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nobutoshi EsakiDepartment of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masami YamamotoLaboratory of Physiological Pathology, Nippon Veterinary and Life Science University, Tokyo, Japan.
Tetsuya TsukamotoDivision of Analytical Pathology, Oncology Innovation Center, Fujita Health University, Toyoake, Japan.
Sachiyo NomuraDepartment of Gastrointestinal Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Takashi MurakamiDepartment of Microbiology, Saitama Medical University, Saitama, Japan.
Masahide TakahashiDepartment of Pathology, Fujita Health University, Toyoake, Japan.
Yuri YuguchiDepartment of Urology, Chukyo Hospital, Nagoya, Japan.
Motohiro MaedaDepartment of Urology, Chukyo Hospital, Nagoya, Japan.
Tomoyasu SanoDepartment of Urology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Naoto SassaDepartment of Urology, Aichi Medical University, Nagakute, Japan.
Yoshihisa MatsukawaDepartment of Urology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Hiroki KawashimaDepartment of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Shusuke AkamatsuDepartment of Urology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Atsushi EnomotoDepartment of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan. enomoto@iar.nagoya-u.ac.jp.ORCID http://orcid.org/0000-0002-9206-6116

Funding

Aichi Cancer Research Foundation (Aichi Cancer Research for the Promotion of Science Foundation) N/AJapan Agency for Medical Research and Development (AMED) 23ck0106779h0002Japan Agency for Medical Research and Development (AMED) 23lk0221167h0001Japan Agency for Medical Research and Development (AMED) 23lk0221172h0001Ministry of Education, Culture, Sports, Science and Technology (MEXT) 22H02848Ministry of Education, Culture, Sports, Science and Technology (MEXT) 22K18390Naito Foundation N/APrincess Takamatsu Cancer Research Fund N/A
6 · The paper itself

Abstract

backgroundThe proliferation of cancer-associated fibroblasts (CAFs) hampers drug delivery and anti-tumor immunity, inducing tumor resistance to immune checkpoint blockade (ICB) therapy. However, it has remained a challenge to develop therapeutics that specifically target or modulate CAFs.

methodsWe investigated the involvement of Meflin

resultsHigh infiltration of Meflin

conclusionOur data suggested that Am80 administration prior to ICB therapy increases the number of Meflin

Indexed as

Cancer-Associated FibroblastsImmune Checkpoint InhibitorsMacrophagesTumor MicroenvironmentAnimalsBenzoatesCarcinoma, Renal CellCell Line, TumorFemaleHumansKidney NeoplasmsMiceRetinoidsTetrahydronaphthalenesTumor-Associated MacrophagesBenzoatesImmune Checkpoint InhibitorsRetinoidstamibaroteneTetrahydronaphthalenes

Identifiers

PMID38849479
PMCPMC11263587

What OpenQuestion holds

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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.