Evidence map›Paper›PMID 28515454›Full record

ArticleScientific reports2017

A quantitative shRNA screen identifies ATP1A1 as a gene that regulates cytotoxicity by aurilide B.

Shohei Takase, Rumi Kurokawa, Daisuke Arai, Kind Kanemoto Kanto, Tatsufumi Okino, Yoichi Nakao, Tetsuo Kushiro, Minoru Yoshida, Ken Matsumoto

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  4. GAS41 promotes H2A.Z deposition through recognition of the N terminus of histone H3 by the YEATS domain.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  8. Article
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  11. Natural Cyclopeptides as Anticancer Agents in the Last 20 Years.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Review
  14. 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

9 authors at 7 institutions in 2 countries.

Shohei TakaseChemical Genomics Research Group, RIKEN Center for Sustainable Resource Science, Saitama, 351-0198, Japan.
Rumi KurokawaChemical Genetics Laboratory, RIKEN, Saitama, 351-0198, Japan.
Daisuke AraiResearch Institute for Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo, 169-8555, Japan.
Kind Kanemoto KantoCollege of Micronesia - FSM Chuuk Campus, P.O. Box 879, Chuuk, 96942, Federated States of Micronesia.
Tatsufumi OkinoFaculty of Environmental Earth Science, Hokkaido University, Sapporo, 060-0810, Japan.ORCID 0000-0002-8363-0467
Yoichi NakaoResearch Institute for Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo, 169-8555, Japan.
Tetsuo KushiroSchool of Agriculture, Meiji University, 1-1-1 Higashimita, Tama-ku, Kawasaki, Kanagawa, 214-8571, Japan.
Minoru YoshidaChemical Genomics Research Group, RIKEN Center for Sustainable Resource Science, Saitama, 351-0198, Japan. yoshidam@riken.jp.
Ken MatsumotoChemical Genomics Research Group, RIKEN Center for Sustainable Resource Science, Saitama, 351-0198, Japan. matsumok@riken.jp.
Meiji University · JPWaseda University · JPCollege of Micronesia-FSM · FMHokkaido University · JPJapan Agency for Medical Research and Development · JPRIKEN · JPRIKEN Center for Sustainable Resource Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-wide RNA interference (RNAi) with pooled and barcoded short-hairpin RNA (shRNA) libraries provides a powerful tool for identifying cellular components that are relevant to the modes/mechanisms of action (MoA) of bioactive compounds. shRNAs that affect cellular sensitivity to a given compound can be identified by deep sequencing of shRNA-specific barcodes. We used multiplex barcode sequencing technology by adding sample-specific index tags to PCR primers during sequence library preparation, enabling parallel analysis of multiple samples. An shRNA library screen with this system revealed that downregulation of ATP1A1, an α-subunit of Na

Indexed as

RNA InterferenceCell Line, TumorCell SurvivalEtoposideGene LibraryHumansPeptides, CyclicPharmacogenomic TestingPharmacogenomic VariantsRNA, Small InterferingSodium-Potassium-Exchanging ATPaseATP1A1 protein, humanaurilide BEtoposidePeptides, CyclicRNA, Small InterferingSodium-Potassium-Exchanging ATPase

Identifiers

PMID28515454
PMCPMC5435677
OpenAlexW2613949295

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.