Evidence map›Paper›PMID 29686061›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Prevention of hepatocellular carcinoma by targeting MYCN-positive liver cancer stem cells with acyclic retinoid.

Xian-Yang Qin, Harukazu Suzuki, Masao Honda, Hikari Okada, Shuichi Kaneko, Ikuyo Inoue, Etsuko Ebisui, Kosuke Hashimoto, Piero Carninci, Keita Kanki and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

70 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Oncogenic function and transcriptional dynamics of MYCN in liver tumorigenesis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Cancer prevention: past challenges and future directions.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 8 institutions in 1 country.

Xian-Yang QinMicro-Signaling Regulation Technology Unit, RIKEN Center for Life Science Technologies, Wako, 351-0198 Saitama, Japan.
Harukazu SuzukiDivision of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, 230-0045 Kanagawa, Japan.
Masao HondaDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, 920-0942 Ishikawa, Japan.
Hikari OkadaDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, 920-0942 Ishikawa, Japan.
Shuichi KanekoDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, 920-0942 Ishikawa, Japan.
Ikuyo InoueMicro-Signaling Regulation Technology Unit, RIKEN Center for Life Science Technologies, Wako, 351-0198 Saitama, Japan.
Etsuko EbisuiMicro-Signaling Regulation Technology Unit, RIKEN Center for Life Science Technologies, Wako, 351-0198 Saitama, Japan.
Kosuke HashimotoDivision of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, 230-0045 Kanagawa, Japan.
Piero CarninciDivision of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, 230-0045 Kanagawa, Japan.
Keita KankiDepartment of Genetic Medicine and Regenerative Therapeutics, Graduate School of Medicine, Tottori University, Yonago, 683-8503 Tottori, Japan.
Hideki TatsukawaDepartment of Basic Medicinal Sciences, Nagoya University Graduate School of Pharmaceutical Sciences, Nagoya, 464-8601 Aichi, Japan.
Naoto IshibashiTokyo New Drug Research Laboratories, Pharmaceutical Division, KOWA Co. Ltd., 189-0022 Tokyo, Japan.
Takahiro MasakiDepartment of Laboratory Medicine, The Jikei University School of Medicine, 105-8461 Tokyo, Japan.
Tomokazu MatsuuraDepartment of Laboratory Medicine, The Jikei University School of Medicine, 105-8461 Tokyo, Japan.
Hiroyuki KagechikaInstitute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 101-0062 Tokyo, Japan.
Kan ToriguchiDepartment of Surgery, Graduate School of Medicine, Kyoto University, 606-8501 Kyoto, Japan.
Etsuro HatanoDepartment of Surgery, Graduate School of Medicine, Kyoto University, 606-8501 Kyoto, Japan.
Yohei ShirakamiDepartment of Gastroenterology, Graduate School of Medicine, Gifu University, 501-1194 Gifu, Japan.
Goshi ShiotaDepartment of Genetic Medicine and Regenerative Therapeutics, Graduate School of Medicine, Tottori University, Yonago, 683-8503 Tottori, Japan.
Masahito ShimizuDepartment of Gastroenterology, Graduate School of Medicine, Gifu University, 501-1194 Gifu, Japan.
Hisataka MoriwakiDepartment of Gastroenterology, Graduate School of Medicine, Gifu University, 501-1194 Gifu, Japan.
Soichi KojimaMicro-Signaling Regulation Technology Unit, RIKEN Center for Life Science Technologies, Wako, 351-0198 Saitama, Japan; skojima@riken.jp.ORCID 0000-0002-5252-1612
RIKEN · JPGifu University · JPKanazawa University · JPJikei University School of Medicine · JPKyoto University · JPTottori University · JPNagoya University · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a highly lethal cancer that has a high rate of recurrence, in part because of cancer stem cell (CSC)-dependent field cancerization. Acyclic retinoid (ACR) is a synthetic vitamin A-like compound capable of preventing the recurrence of HCC. Here, we performed a genome-wide transcriptome screen and showed that ACR selectively suppressed the expression of MYCN, a member of the MYC family of basic helix-loop-helix-zipper transcription factors, in HCC cell cultures, animal models, and liver biopsies obtained from HCC patients. MYCN expression in human HCC was correlated positively with both CSC and Wnt/β-catenin signaling markers but negatively with mature hepatocyte markers. Functional analysis showed repressed cell-cycle progression, proliferation, and colony formation, activated caspase-8, and induced cell death in HCC cells following silencing of MYCN expression. High-content single-cell imaging analysis and flow cytometric analysis identified a MYCN

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, HepatocellularEpithelial Cell Adhesion MoleculeGene Expression Regulation, NeoplasticHumansLiver NeoplasmsNeoplasm MetastasisNeoplastic Stem CellsN-Myc Proto-Oncogene ProteinPrognosisTretinoinWnt Signaling Pathway3,7,11,15-tetramethyl-2,4,6,10,14-hexadecapentaenoic acidAntineoplastic AgentsEPCAM protein, humanEpithelial Cell Adhesion MoleculeMYCN protein, humanN-Myc Proto-Oncogene ProteinTretinoinacyclic retinoidcancer stem cellhepatocellular carcinomaMYCNtranscriptome

Identifiers

PMID29686061
PMCPMC5949003
OpenAlexW2801937548

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.