Evidence map›Paper›PMID 38474369›Full record

ArticleCells2024

Pronecroptotic Therapy Using Ceramide Nanoliposomes Is Effective for Triple-Negative Breast Cancer Cells.

Yuki Ohya, Yuri Ogiso, Masaya Matsuda, Harumi Sakae, Kentaro Nishida, Yasuhiro Miki, Todd E Fox, Mark Kester, Wataru Sakamoto, Takeshi Nabe and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
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

11 authors at 4 institutions in 2 countries.

Yuki OhyaFaculty of Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Japan.
Yuri OgisoFaculty of Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Japan.
Masaya MatsudaFaculty of Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Japan.ORCID 0000-0001-6498-8335
Harumi SakaeFaculty of Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Japan.
Kentaro NishidaFaculty of Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Japan.
Yasuhiro MikiDepartment of Pathology, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.ORCID 0000-0003-3618-5652
Todd E FoxDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908-8735, USA.ORCID 0000-0001-5170-3951
Mark KesterDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908-8735, USA.
Wataru SakamotoResearch Center of Oncology, Ono Pharmaceutical, Co., Ltd., Osaka 618-8585, Japan.
Takeshi NabeFaculty of Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Japan.
Kazuyuki KitataniFaculty of Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Japan.ORCID 0000-0002-8516-6135
Setsunan University · JPUniversity of Virginia · USOno Pharmaceutical (Japan) · JPTohoku University · JP

Funding

Japan Society for the Promotion of Science 40539235
6 · The paper itself

Abstract

Regulated necrosis, termed necroptosis, represents a potential therapeutic target for refractory cancer. Ceramide nanoliposomes (CNLs), considered potential chemotherapeutic agents, induce necroptosis by targeting the activating protein mixed lineage kinase domain-like protein (MLKL). In the present study, we examined the potential of pronecroptotic therapy using CNLs for refractory triple-negative breast cancer (TNBC), for which there is a lack of definite and effective therapeutic targets among the various immunohistological subtypes of breast cancer. MLKL mRNA expression in tumor tissues was significantly higher in TNBC patients than in those with non-TNBC subtypes. Similarly, among the 50 breast cancer cell lines examined, MLKL expression was higher in TNBC-classified cell lines. TNBC cell lines were more susceptible to the therapeutic effects of CNLs than the non-TNBC subtypes of breast cancer cell lines. In TNBC-classified MDA-MB-231 cells, the knockdown of MLKL suppressed cell death induced by CNLs or the active substance short-chain C

Indexed as

Triple Negative Breast NeoplasmsApoptosisCell Line, TumorCeramidesHumansNecrosisCeramidesbreast cancerceramideceramide nanoliposomemixed-lineage kinase domain-like proteinnecroptosistriple-negative breast cancer

Identifiers

PMID38474369
PMCPMC10931450
OpenAlexW4392169743

What OpenQuestion holds

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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.