Evidence map›Paper›PMID 30894572›Full record

ArticleScientific reports2019

RNAi Screening-based Identification of USP10 as a Novel Regulator of Paraptosis.

Jin Yeop Kim, Dong Min Lee, Hyun Goo Woo, Ki Deok Kim, Hong Jae Lee, Yong-Jun Kwon, Kyeong Sook Choi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. 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
0.5field-weighted citation impact, top 36% 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, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Paraptosis-A Distinct Pathway to Cell Death.International journal of molecular sciences · 2024
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Deubiquitinases: Modulators of Different Types of Regulated Cell Death.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Article
  17. Ubiquitin-Specific Protease 10: A New Target in Tumor Immune Escape.Cancer control : journal of the Moffitt Cancer Center
    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

7 authors at 2 institutions in 2 countries.

Jin Yeop KimDepartment of Biomedical Sciences, Department of Biochemistry and Molecular biology, Ajou University Graduate School of Medicine, 16499, Suwon, Korea.
Dong Min LeeDepartment of Biomedical Sciences, Department of Biochemistry and Molecular biology, Ajou University Graduate School of Medicine, 16499, Suwon, Korea.
Hyun Goo WooDepartment of Physiology, Department of Biomedical Sciences, Ajou University School of Medicine, Suwon, Korea.ORCID 0000-0002-0916-893X
Ki Deok KimInstitut Pasteur Korea, Seongnam, Korea.
Hong Jae LeeDepartment of Biomedical Sciences, Department of Biochemistry and Molecular biology, Ajou University Graduate School of Medicine, 16499, Suwon, Korea.
Yong-Jun KwonInstitut Pasteur Korea, Seongnam, Korea. yjkwonipk@gmail.com.
Kyeong Sook ChoiDepartment of Biomedical Sciences, Department of Biochemistry and Molecular biology, Ajou University Graduate School of Medicine, 16499, Suwon, Korea. kschoi@ajou.ac.kr.
Ajou University · KRInstitut Pasteur Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating reports demonstrate that apoptosis does not explain all the effects of cancer therapy due to the innate and acquired apoptotic resistance of malignant cancer cells. Recently, paraptosis, a type of programmed cell death accompanied by dilation of mitochondria and/or the endoplasmic reticulum (ER), has garnered interest in cancer research as an alternative way to kill apoptosis-resistant cancers. We describe here the adaptation and validation of a high-content cell-based assay to screen and identify novel paraptotic regulators employing the malignant breast cancer cells undergoing curcumin-induced paraptosis. We used YFP-Mito cells, which express fluorescence selectively in mitochondria, to select paraptosis-related genes whose corresponding siRNAs appeared to modulate mitochondrial dilation, a morphological feature of paraptosis. From the selected 38 candidate genes, we chose ubiquitin specific peptidase 10 (USP10), a ubiquitin specific protease, as a strongly active candidate that warranted further evaluation of its involvement in paraptosis. We found that both siRNA-mediated knockdown of USP10 and treatment with the USP10 inhibitor, spautin-1, effectively attenuated curcumin-induced paraptosis. This systematic assay, in which a siRNA library is screened for the ability to ameliorate paraptotic changes in mitochondria, may enable researchers to identify potent regulators of paraptosis and new candidate genes/drugs to combat malignant breast cancer.

Indexed as

Antineoplastic AgentsBenzylaminesBreast NeoplasmsCell DeathCell Line, TumorCurcuminEndoplasmic ReticulumFemaleGene LibraryHigh-Throughput Screening AssaysHumansMembrane Potential, MitochondrialMitochondriaQuinazolinesRNA InterferenceRNA, Small InterferingAntineoplastic AgentsBenzylaminesCurcuminQuinazolinesRNA, Small Interferingspautin-1Ubiquitin ThiolesteraseUSP10 protein, human

Identifiers

PMID30894572
PMCPMC6427038
OpenAlexW2922705025

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.