Evidence map›Paper›PMID 38760458›Full record

ArticleScientific reports2024

Isobutyric acid enhances the anti-tumour effect of anti-PD-1 antibody.

Masakazu Murayama, Masahiro Hosonuma, Atsuo Kuramasu, Sei Kobayashi, Akiko Sasaki, Yuta Baba, Yoichiro Narikawa, Hitoshi Toyoda, Junya Isobe, Eiji Funayama and 23 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–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.

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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  16. Association between theMicrobiology spectrum · 2025
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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

33 authors.

Masakazu MurayamaDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Masahiro HosonumaDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Atsuo KuramasuDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Sei KobayashiDepartment of Otorhinolaryngology, Fujigaoka Hospital, Yokohama, Japan.
Akiko SasakiDivision of Medical Pharmacology, Department of Pharmacology, Showa University School of Medicine, Tokyo, Japan.
Yuta BabaDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Yoichiro NarikawaDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Hitoshi ToyodaDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Junya IsobeDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan.
Eiji FunayamaDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Kohei TajimaDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Aya SasakiDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Yuki MaruyamaDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Yoshitaka YamazakiPharmacological Research Center, Showa University, Tokyo, Japan.
Midori ShidaDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Kazuyuki HamadaDivision of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Yuya HirasawaDivision of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Toshiaki TsuruiDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan.
Hirotsugu AriizumiDivision of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Tomoyuki IshiguroDivision of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Risako SuzukiDivision of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Ryotaro OhkumaDivision of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Yutaro KubotaDivision of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Atsushi HoriikeDivision of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Takehiko SambeDivision of Clinical Pharmacology, Department of Pharmacology, Showa University School of Medicine, Tokyo, Japan.
Mayumi TsujiPharmacological Research Center, Showa University, Tokyo, Japan.
Satoshi WadaDepartment of Clinical Diagnostic Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.
Shinichi KobayashiClinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.
Toshikazu ShimaneHead and Neck Oncology Center, Showa University, Tokyo, Japan.
Takuya TsunodaDivision of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Hitome KobayashiDepartment of Otorhinolaryngology-Head and Neck Surgery, Showa University School of Medicine, Tokyo, Japan.
Yuji KiuchiDivision of Medical Pharmacology, Department of Pharmacology, Showa University School of Medicine, Tokyo, Japan.
Kiyoshi YoshimuraDepartment of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, 6-11-11, Kitakarasuyama, Setagaya-ku, Tokyo, 157-8577, Japan. kyoshim1@med.showa-u.ac.jp.

Funding

Grant-in-Aid for Scientific Research (C) 22K09675
6 · The paper itself

Abstract

The low response rate of immune checkpoint inhibitors (ICIs) is a challenge. The efficacy of ICIs is influenced by the tumour microenvironment, which is controlled by the gut microbiota. In particular, intestinal bacteria and their metabolites, such as short chain fatty acids (SCFAs), are important regulators of cancer immunity; however, our knowledge on the effects of individual SCFAs remains limited. Here, we show that isobutyric acid has the strongest effect among SCFAs on both immune activity and tumour growth. In vitro, cancer cell numbers were suppressed by approximately 75% in humans and mice compared with those in controls. Oral administration of isobutyric acid to carcinoma-bearing mice enhanced the effect of anti-PD-1 immunotherapy, reducing tumour volume by approximately 80% and 60% compared with those in the control group and anti-PD-1 antibody alone group, respectively. Taken together, these findings may support the development of novel cancer therapies that can improve the response rate to ICIs.

Indexed as

Immune Checkpoint InhibitorsIsobutyratesProgrammed Cell Death 1 ReceptorTumor MicroenvironmentAnimalsCell Line, TumorDrug SynergismFatty Acids, VolatileFemaleGastrointestinal MicrobiomeHumansImmunotherapyMiceNeoplasmsFatty Acids, VolatileImmune Checkpoint InhibitorsIsobutyratesisobutyric acidProgrammed Cell Death 1 Receptor

Identifiers

PMID38760458
PMCPMC11101641

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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.