Evidence map›Paper›PMID 24900207›Full record

ArticleACS medicinal chemistry letters2010

KSRP/FUBP2 Is a Binding Protein of GO-Y086, a Cytotoxic Curcumin Analogue.

Hiroyuki Yamakoshi, Naoki Kanoh, Chieko Kudo, Atsuko Sato, Kazunori Ueda, Makoto Muroi, Shunsuke Kon, Masanobu Satake, Hisatsugu Ohori, Chikashi Ishioka and 5 more

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 23 citations in OpenAlex.

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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

15 authors at 4 institutions in 2 countries.

Hiroyuki YamakoshiGraduate School of Pharmaceutical Sciences.
Naoki KanohGraduate School of Pharmaceutical Sciences.
Chieko KudoInstitute of Development, Aging and Cancer.
Atsuko SatoInstitute of Development, Aging and Cancer.
Kazunori UedaGraduate School of Pharmaceutical Sciences.
Makoto MuroiChemical Biology Department, Advanced Science Institute, RIKEN, Wako, Saitama 351-0198, Japan.
Shunsuke KonInstitute of Development, Aging and Cancer.
Masanobu SatakeInstitute of Development, Aging and Cancer.
Hisatsugu OhoriInstitute of Development, Aging and Cancer.
Chikashi IshiokaInstitute of Development, Aging and Cancer.
Yoshiteru OshimaGraduate School of Pharmaceutical Sciences.
Hiroyuki OsadaChemical Biology Department, Advanced Science Institute, RIKEN, Wako, Saitama 351-0198, Japan.
Natsuko ChibaInstitute of Development, Aging and Cancer.
Hiroyuki ShibataDepartment of Clinical Oncology, Akita University Hospital, Akita 010-8543, Japan.
Yoshiharu IwabuchiGraduate School of Pharmaceutical Sciences.
Institute of Aging · CAKumamoto University · JPRIKEN Advanced Science Institute · JPAkita University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bis(arylmethylidene)acetone derivatives are an important class of curcumin analogues that exhibit various biological and pharmacological activities. We herein report that GO-Y086, a biotinylated bis(arylmethylidene)acetone, inhibits cancer cell growth. We also show that GO-Y086 specifically interacts with the nuclear protein KSRP/FUBP2 by covalent modification. GO-Y086 markedly suppresses the expression of the c-Myc protein, which plays an important role in cellular proliferation and whose expression is regulated by KSRP/FUBP2.

Indexed as

anticancerbis(arylmethylidene)acetonec-Myccurcumin analogueKSRP/FUBP2target protein

Identifiers

PMID24900207
PMCPMC4007841
OpenAlexW1996876030

What OpenQuestion holds

Textmetadata
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.