Evidence map›Paper›PMID 28192620›Full record

ArticleCancer science2017

YPC-21661 and YPC-22026, novel small molecules, inhibit ZNF143 activity in vitro and in vivo.

Hirotaka Haibara, Ryuta Yamazaki, Yukiko Nishiyama, Masahiro Ono, Tsuneyuki Kobayashi, Atsuko Hokkyo-Itagaki, Fukiko Nishisaka, Hiroyuki Nishiyama, Akinobu Kurita, Takeshi Matsuzaki and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. ZNF143 Expression is Associated with COPD and Tumor Microenvironment in Non-Small Cell Lung Cancer.International journal of chronic obstructive pulmonary disease · 2022
    Article
  7. 1,3,4-OxadiazoleMolecules (Basel, Switzerland) · 2021
    Article
  8. Article
  9. Article
  10. Oncology letters · 2020
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

12 authors at 2 institutions in 1 country.

Hirotaka HaibaraYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.ORCID http://orcid.org/0000-0001-5492-0134
Ryuta YamazakiYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.
Yukiko NishiyamaYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.
Masahiro OnoYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.
Tsuneyuki KobayashiYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.
Atsuko Hokkyo-ItagakiYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.
Fukiko NishisakaYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.
Hiroyuki NishiyamaYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.
Akinobu KuritaYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.
Takeshi MatsuzakiYakult Central Institute, Yakult Honsha Co., Ltd., Kunitachi, Tokyo, Japan.
Hiroto IzumiThe University of Occupational and Environmental Health, Kitakyushu, Japan.
Kimitoshi KohnoThe University of Occupational and Environmental Health, Kitakyushu, Japan.
Yakult Honsha (Japan) · JPUniversity of Occupational and Environmental Health Japan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zinc-finger protein 143 (ZNF143) is a transcription factor that is involved in anticancer drug resistance and cancer cell survival. In the present study, we identified a novel small molecule N-(5-bromo-2-methoxyphenyl)-3-(pyridine-3-yl) propiolamide (YPC-21661) that inhibited ZNF143 promoter activity and down-regulated the expression of the ZNF143-regulated genes, RAD51, PLK1, and Survivin, by inhibiting the binding of ZNF143 to DNA. In addition, YPC-21661 was cytotoxic and induced apoptosis in the human colon cancer cell line, HCT116 and human prostate cancer cell line, PC-3. 2-(pyridine-3-ylethynyl)-5-(2-(trifluoromethoxy)phenyl)-1,3,4-oxadiazole (YPC-22026), a metabolically stable derivative of YPC-21661, induced tumor regression accompanied by the suppression of ZNF143-regulated genes in a mouse xenograft model. The present study revealed that the inhibition of ZNF143 activity by small molecules induced tumor regression in vitro and in vivo; therefore, ZNF143 is a promising target of cancer therapeutics.

Indexed as

AnimalsApoptosisCell Line, TumorCell SurvivalColonic NeoplasmsHCT116 CellsHT29 CellsHumansMaleMiceMice, Inbred BALB CMice, NudePromoter Regions, GeneticProstatic NeoplasmsSignal TransductionSmall Molecule LibrariesSmall Molecule LibrariesTrans-ActivatorsTranscription FactorsZNF143 protein, humananticancer drugapoptosiscell cycletranscription factorZNF143

Identifiers

PMID28192620
PMCPMC5448606
OpenAlexW2588339892

What OpenQuestion holds

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LicenceCC BY-NC
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.