Evidence map›Paper›PMID 28693221›Full record

ArticleOncology letters2017

Fatty acids inhibit anticancer effects of 5-fluorouracil in mouse cancer cell lines.

Eriko Tanabe, Misaho Kitayoshi, Kiyomu Fujii, Hitoshi Ohmori, Yi Luo, Yui Kadochi, Shiori Mori, Rina Fujiwara, Yukiko Nishiguchi, Takamitsu Sasaki and 1 more

Expression of concernOpen access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Elevated CCL20 and IL-10 enhance 5-fluorouracil tolerance in colon cancer.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2025
    Article
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  8. Review
  9. Effect of Proton Pump Inhibitors on Colorectal Cancer.International journal of molecular sciences · 2020
    Article
  10. Article
  11. Article
  12. Pro-metastatic signaling of theOncology letters · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Eriko TanabeDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Misaho KitayoshiDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Kiyomu FujiiDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Hitoshi OhmoriDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Yi LuoDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Yui KadochiDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Shiori MoriDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Rina FujiwaraDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Yukiko NishiguchiDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Takamitsu SasakiDepartment of Gastroenterological Surgery, Fukuoka University School of Medicine, Fukuoka 814-0133, Japan.
Hiroki KuniyasuDepartment of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Nara Medical University · JPFukuoka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study investigated the effects of two major dietary fatty acid components, linoleic acid (LA) and elaidic acid (EA), on the antitumor effects of 5-fluorouracil (5-FU) in the LL2, CT26 and CMT93 mouse cancer cell lines. Concurrent treatment with LA and 5-FU elicited a decreased cell viability compared with treatment with 5-FU alone. In addition, increased inhibition of growth was observed following concurrent treatment with EA and 5-FU. Sequential treatment of LA followed by 5-FU abrogated the anticancer effects of 5-FU, and treatment with EA followed by 5-FU increased cancer cell growth in addition to abrogating the anticancer effects of 5-FU. The expression of the stem cell markers CD133 and nucleostemin (NS) increased in all three cell lines treated concurrently with 5-FU and either LA or EA when compared with cells treated with 5-FU alone. Aldehyde dehydrogenase activity in the cancer stem cells (CSCs), in response to concurrent treatment with 5-FU and either LA or EA, was increased compared with 5-FU treatment alone. 5-FU inhibited the growth of CT26 tumors, but co-treatment with either LA or EA abrogated this effect. NS-positive CSCs were more abundant in CT26 tumors treated with 5-FU and either LA or EA compared with those treated with 5-FU alone. The results of the present study suggested that, rather than altering the sensitivity of cancer cells to 5-FU, LA and EA may promote the survival of CSCs. The results indicated that dietary composition during chemotherapy is an important issue.

Indexed as

cancer stem cellschemotherapyfatty acid

Identifiers

PMID28693221
PMCPMC5494753
OpenAlexW2614683380

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.