Evidence map›Paper›PMID 40076581›Full record

ArticleInternational journal of molecular sciences2025

Anti-Cancer and Pro-Immune Effects of Lauric Acid on Colorectal Cancer Cells.

Shiori Mori, Rina Fujiwara-Tani, Ruiko Ogata, Hitoshi Ohmori, Kiyomu Fujii, Yi Luo, Takamitsu Sasaki, Yukiko Nishiguchi, Ujjal Kumar Bhawal, Shingo Kishi and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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.

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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
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

11 authors.

Shiori MoriDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.
Rina Fujiwara-TaniDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.
Ruiko OgataDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.
Hitoshi OhmoriDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.
Kiyomu FujiiDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.
Yi LuoDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.
Takamitsu SasakiDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.
Yukiko NishiguchiDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.
Ujjal Kumar BhawalResearch Institute of Oral Science, School of Dentistry at Matsudo, Nihon University, Matsudo 271-8587, Japan.ORCID 0000-0002-3746-009X
Shingo KishiDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.
Hiroki KuniyasuDepartment of Molecular Pathology, School of Medicine, Nara Medical University, Kashihara 634-8521, Japan.ORCID 0000-0003-2298-8825

Funding

Ministry of Education, Culture, Sports, Science and Technology 19K16564Ministry of Education, Culture, Sports, Science and Technology 20K21659Ministry of Education, Culture, Sports, Science and Technology 21K06926Ministry of Education, Culture, Sports, Science and Technology 21K11223Ministry of Education, Culture, Sports, Science and Technology 22K16497Ministry of Education, Culture, Sports, Science and Technology 23K10481Ministry of Education, Culture, Sports, Science and Technology 23K16621
6 · The paper itself

Abstract

Lauric acid (LAA) is a 12-carbon medium-chain fatty acid that reportedly has antitumor and muscle-protecting effects. However, the details of these antitumor effects remain unclear. Therefore, in this study, we investigated the mechanism underlying the antitumor effects of LAA in CT26 and HT29 colorectal cancer (CRC) cell lines. Our in vitro findings demonstrated that LAA suppressed CRC cell proliferation, induced mitochondrial oxidative stress (reactive oxygen species (ROS)), inhibited oxidative phosphorylation (OXPHOS), and induced apoptosis. Moreover, in vivo analysis of LAA showed a more pronounced antitumor effect in CT26 cells in a syngeneic mouse tumor model than in vitro; therefore, we further investigated its impact on host antitumor immunity. We observed that LAA increased the number of effector T cells in mouse tumors, while in vitro LAA activated mouse splenocytes (SplC) and promoted OXPHOS. In two-dimensional co-culture of SplC and CT26 cells, LAA induced cell death in cancer cells. In three-dimensional co-culture, LAA promoted SplC infiltration and suppressed the formation of tumor spheres. Thus, LAA may exert antitumor effects through increased ROS production in cancer cells and effector T cell activation via increased energy metabolism. These results suggest that LAA, when used in combination with existing anti-cancer drugs, is likely to exhibit sensitizing effects in terms of both antitumor and antitumor immune effects, and future clinical studies are anticipated.

Indexed as

Antineoplastic AgentsColorectal NeoplasmsLauric AcidsAnimalsApoptosisCell Line, TumorCell ProliferationCoculture TechniquesHT29 CellsHumansMiceMitochondriaOxidative PhosphorylationOxidative StressReactive Oxygen SpeciesAntineoplastic Agentslauric acidLauric AcidsReactive Oxygen Speciesanti-cancer immunitycolorectal cancerenergy metabolismlauric acidoxidative stress

Identifiers

PMID40076581
PMCPMC11901037

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Registered trials

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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.