Evidence map›Paper›PMID 26396918›Full record

ArticleAmerican journal of cancer research2015

Novel 5-fluorouracil-resistant human esophageal squamous cell carcinoma cells with dihydropyrimidine dehydrogenase overexpression.

Osamu Kikuchi, Shinya Ohashi, Yukie Nakai, Shunsaku Nakagawa, Kazuaki Matsuoka, Takashi Kobunai, Teiji Takechi, Yusuke Amanuma, Masahiro Yoshioka, Tomomi Ida and 7 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
  2. GermlineeLife · 2024
    Article
  3. GermlinebioRxiv : the preprint server for biology · 2024
    Article
  4. Review
  5. Molecular mechanisms associated with chemoresistance in esophageal cancer.Cellular and molecular life sciences : CMLS · 2022
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
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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

17 authors at 2 institutions in 1 country.

Osamu KikuchiDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Shinya OhashiDepartment of Therapeutic Oncology, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Yukie NakaiDepartment of Therapeutic Oncology, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Shunsaku NakagawaDepartment of Pharmacy, Kyoto University Hospital Kyoto 606-8507, Japan.
Kazuaki MatsuokaTranslational Research Laboratory, Taiho Pharmaceutical Co., Ltd. Tokushima 771-0194, Japan.
Takashi KobunaiTranslational Research Laboratory, Taiho Pharmaceutical Co., Ltd. Tokushima 771-0194, Japan.
Teiji TakechiTranslational Research Laboratory, Taiho Pharmaceutical Co., Ltd. Tokushima 771-0194, Japan.
Yusuke AmanumaDepartment of Therapeutic Oncology, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Masahiro YoshiokaDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Tomomi IdaDepartment of Therapeutic Oncology, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan ; Department of Clinical Systems Onco-Informatics, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Yoshihiro YamamotoDepartment of Clinical Systems Onco-Informatics, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Yasushi OkunoDepartment of Clinical Systems Onco-Informatics, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Shin'ichi MiyamotoDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Hiroshi NakagawaGastroenterology Division, Department of Medicine, Abramson Cancer Center, University of Pennsylvania Philadelphia, Pennsylvania 19104, USA.
Kazuo MatsubaraDepartment of Pharmacy, Kyoto University Hospital Kyoto 606-8507, Japan.
Tsutomu ChibaDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Manabu MutoDepartment of Therapeutic Oncology, Kyoto University Graduate School of Medicine Kyoto 606-8507, Japan.
Kyoto University · JPKyoto University Hospital · JP

Funding

TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 1997 to 2026
$32.5M
Transformed Esophageal Epithelial Cells and the Tumor MicroenvironmentP01CA098101 · NCI · UNIVERSITY OF PENNSYLVANIA · PI HIBSHOOSH, HANINA · 2003 to 2023
$31.7M
Integrative mouse pathobiology: GI epithelial biology and geneticsK26RR032714 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI NAKAGAWA, HIROSHI · 2011 to 2011
$87k
NCI NIH HHS P01 CA098101NCRR NIH HHS K26 RR032714NIDDK NIH HHS P30 DK050306
6 · The paper itself

Abstract

5-Fluorouracil (5-FU) is a key drug for the treatment of esophageal squamous cell carcinoma (ESCC); however, resistance to it remains a critical limitation to its clinical use. To clarify the mechanisms of 5-FU resistance of ESCC, we originally established 5-FU-resistant ESCC cells, TE-5R, by step-wise treatment with continuously increasing concentrations of 5-FU. The half maximal inhibitory concentration of 5-FU showed that TE-5R cells were 15.6-fold more resistant to 5-FU in comparison with parental TE-5 cells. TE-5R cells showed regional copy number amplification of chromosome 1p including the DPYD gene, as well as high mRNA and protein expressions of dihydropyrimidine dehydrogenase (DPD), an enzyme involved in 5-FU degradation. 5-FU treatment resulted in a significant decrease of the intracellular 5-FU concentration and increase of the concentration of α-fluoro-ureidopropionic acid (FUPA), a metabolite of 5-FU, in TE-5R compared with TE-5 cells in vitro. Conversely, gimeracil, a DPD inhibitor, markedly increased the intracellular 5-FU concentration, decreased the intracellular FUPA concentration, and attenuated 5-FU resistance of TE-5R cells. These results indicate that 5-FU resistance of TE-5R cells is due to the rapid degradation of 5-FU by DPD overexpression. The investigation of 5-FU-resistant ESCC with DPYD gene copy number amplification and consequent DPD overexpression may generate novel biological evidence to explore strategies against ESCC with 5-FU resistance.

Indexed as

5-fluorouracilchemotherapydihydropyrimidine dehydrogenasedrug resistanceEsophageal squamous cell carcinoma

Identifiers

PMID26396918
PMCPMC4568778
OpenAlexW2411858480

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.