Evidence map›Paper›PMID 31555951›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2020

Epigenetic priming sensitizes gastric cancer cells to irinotecan and cisplatin by restoring multiple pathways.

Hiroshi Moro, Naoko Hattori, Yoshiaki Nakamura, Kana Kimura, Toshio Imai, Masahiro Maeda, Masakazu Yashiro, Toshikazu Ushijima

Erratum issued Registry-linked trialOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT05381038 (Optimizing and Personalising Azacitidine Combination Therapy for Treating Solid Tumours Using the Quadratic Phenotypic Optimization Platform), 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
1.6field-weighted citation impact, top 16% 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.

NCT05381038 phase1 / phase2recruitingnot on this mapstarted 2023, after this paper: background citation

Optimizing and Personalising Azacitidine Combination Therapy for Treating Solid Tumours Using the Quadratic Phenotypic Optimization Platform (QPOP) and an Artificial Intelligence-based Platform (CURATE.AI)

TypeinterventionalSponsorNational University Hospital, SingaporeRan2023 to 2027Enrolled10ConditionsSolid Tumor, Gastrointestinal Cancer, Breast CancerArmsQPOP, CURATE.AI, Azacitidine + docetaxel, Azacitidine + paclitaxel, Azacitidine + irinotecan
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Getting the right combination to break the epigenetic code.Nature reviews. Clinical oncology · 2025
    Review
  4. Gastric Cancer in the Era of Epigenetics.International journal of molecular sciences · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Frontiers in oncology · 2021
    Review
  15. Review
  16. Article
  17. Review
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Hiroshi MoroDivision of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan.
Naoko HattoriDivision of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan.
Yoshiaki NakamuraDivision of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan.
Kana KimuraDivision of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan.
Toshio ImaiCentral Animal Division, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Masahiro MaedaDivision of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan.
Masakazu YashiroDepartment of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka, Japan.
Toshikazu UshijimaDivision of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan. tushijim@ncc.go.jp.ORCID http://orcid.org/0000-0003-3405-7817
Juntendo University · JPNational Cancer Center Hospital East · JPNational Cancer Centre Japan · JPOsaka City University · JP

Funding

Japan Agency for Medical Research and Development JP19ck0106421
6 · The paper itself

Abstract

backgroundGastric cancer is heavily influenced by aberrant DNA methylation that alters multiple cancer-related pathways, and may respond to DNA demethylating agents, such as 5-aza-2'-deoxycytidine (5-aza-dC). Here, we aimed to analyze whether 5-aza-dC can sensitize gastric cancer cells to clinically used cytotoxic drugs.

methodsTen gastric cancer cell lines were treated with 5-aza-dC for 72 h and their growth was analyzed by conducting WST assay. In vivo effect of the drugs was analyzed using xenografts of OCUM-2 M/SN38 cells. Genome-wide expression and DNA methylation analyses were conducted using microarrays, and biological functions were identified through ingenuity pathway analysis.

resultsThe cell lines most resistant to SN38 (an active metabolite of irinotecan), CDDP, PTX, and 5-FU, were identified. 5-Aza-dC pre-treatment of the resistant cell lines decreased the IC

conclusionEpigenetic priming with 5-aza-dC can improve the sensitivity of gastric cancer cells to SN38 and CDDP.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorCisplatinDecitabineDNA MethylationDrug Resistance, NeoplasmEpigenesis, GeneticFemaleGene Expression Regulation, NeoplasticHumansIrinotecanMice, NudeStomach NeoplasmsXenograft Model Antitumor AssaysCisplatinDecitabineIrinotecanCisplatinDecitabineDNA methylationIrinotecanResistance

Identifiers

PMID31555951
OpenAlexW2975799428

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.