Evidence map›Paper›PMID 29079707›Full record

ArticleMolecular cancer therapeutics2018

Ceramide Nanoliposomes as a MLKL-Dependent, Necroptosis-Inducing, Chemotherapeutic Reagent in Ovarian Cancer.

Xuewei Zhang, Kazuyuki Kitatani, Masafumi Toyoshima, Masumi Ishibashi, Toshinori Usui, Junko Minato, Mahy Egiz, Shogo Shigeta, Todd Fox, Tye Deering and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

36 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Establishment of a Prognostic Necroptosis-Related lncRNA Signature in Ovarian Cancer.Combinatorial chemistry & high throughput screening · 2026
    Article
  4. Article
  5. Drug Resistance: The Role of Sphingolipid Metabolism.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Sphingolipid metabolism and regulated cell death in malignant melanoma.Apoptosis : an international journal on programmed cell death · 2024
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Necroptosis pathways in tumorigenesis.Seminars in cancer biology · 2022
    Review
  20. Necroptosis: A Pathogenic Negotiator in Human Diseases.International journal of molecular sciences · 2022
    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 1 institution in 1 country.

Xuewei ZhangDepartment of Obstetrics and Gynecology, Tohoku University School of Medicine, Tohoku University, Sendai, Japan.
Kazuyuki KitataniDepartment of Obstetrics and Gynecology, Tohoku University School of Medicine, Tohoku University, Sendai, Japan. kitatani@med.tohoku.ac.jp m-toyo@med.tohoku.ac.jp.
Masafumi ToyoshimaDepartment of Obstetrics and Gynecology, Tohoku University School of Medicine, Tohoku University, Sendai, Japan. kitatani@med.tohoku.ac.jp m-toyo@med.tohoku.ac.jp.
Masumi IshibashiDepartment of Obstetrics and Gynecology, Tohoku University School of Medicine, Tohoku University, Sendai, Japan.
Toshinori UsuiTohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
Junko MinatoDepartment of Obstetrics and Gynecology, Tohoku University School of Medicine, Tohoku University, Sendai, Japan.
Mahy EgizDepartment of Obstetrics and Gynecology, Tohoku University School of Medicine, Tohoku University, Sendai, Japan.
Shogo ShigetaDepartment of Obstetrics and Gynecology, Tohoku University School of Medicine, Tohoku University, Sendai, Japan.
Todd FoxDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia.
Tye DeeringDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia.
Mark KesterDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia.
Nobuo YaegashiDepartment of Obstetrics and Gynecology, Tohoku University School of Medicine, Tohoku University, Sendai, Japan.
University of Virginia · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Jay William FOX · 1987 to 2026
$72.1M
Tissue Repository and Animal Models CoreP01CA171983 · NCI · UNIVERSITY OF VIRGINIA · PI FISHER-WELLMAN, KELSEY H · 2013 to 2024
$19.9M
NCI NIH HHS P01 CA171983NCI NIH HHS P30 CA044579
6 · The paper itself

Abstract

Ceramides are bioactive lipids that mediate cell death in cancer cells, and ceramide-based therapy is now being tested in dose-escalating phase I clinical trials as a cancer treatment. Multiple nanoscale delivery systems for ceramide have been proposed to overcome the inherent toxicities, poor pharmacokinetics, and difficult biophysics associated with ceramide. Using the ceramide nanoliposomes (CNL), we now investigate the therapeutic efficacy and signaling mechanisms of this nanoscale delivery platform in refractory ovarian cancer. Treatment of ovarian cancer cells with CNL decreased the number of living cells through necroptosis but not apoptosis. Mechanistically, dying SKOV3 ovarian cancer cells exhibit activation of pseudokinase mixed lineage kinase domain-like (MLKL) as evidenced by oligomerization and relocalization to the blebbing membranes, showing necroptotic characteristics. Knockdown of MLKL, but not its upstream protein kinases such as receptor-interacting protein kinases, with siRNA significantly abolished CNL-induced cell death. Monomeric MLKL protein expression inversely correlated with the IC

Indexed as

ApoptosisCeramidesFemaleHumansNecrosisOvarian NeoplasmsProtein KinasesTransfectionCeramidesMLKL protein, humanProtein Kinases

Identifiers

PMID29079707
PMCPMC5752574
OpenAlexW2766941807

What OpenQuestion holds

Textmetadata
LicenceTDM
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.