Evidence map›Paper›PMID 29330434›Full record

ArticleScientific reports2018

Targeting melanoma stem cells with the Vitamin E derivative δ-tocotrienol.

Monica Marzagalli, Roberta Manuela Moretti, Elio Messi, Marina Montagnani Marelli, Fabrizio Fontana, Alessia Anastasia, Maria Rosa Bani, Giangiacomo Beretta, Patrizia Limonta

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. CaApoptosis : an international journal on programmed cell death · 2021
    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

9 authors.

Monica MarzagalliDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milano, 20133, Italy.
Roberta Manuela MorettiDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milano, 20133, Italy.
Elio MessiDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milano, 20133, Italy.
Marina Montagnani MarelliDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milano, 20133, Italy.
Fabrizio FontanaDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milano, 20133, Italy.
Alessia AnastasiaLaboratory of Biology and Treatment of Metastasis, IRCCS-Mario Negri Institute for Pharmacological Research, Milano, 20156, Italy.
Maria Rosa BaniLaboratory of Biology and Treatment of Metastasis, IRCCS-Mario Negri Institute for Pharmacological Research, Milano, 20156, Italy.
Giangiacomo BerettaDepartment of Pharmaceutical Sciences, Università degli Studi di Milano, Milano, 20133, Italy.
Patrizia LimontaDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milano, 20133, Italy. patrizia.limonta@unimi.it.ORCID http://orcid.org/0000-0001-7028-3008

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of metastatic melanoma is very poor, due to the development of drug resistance. Cancer stem cells (CSCs) may play a crucial role in this mechanism, contributing to disease relapse. We first characterized CSCs in melanoma cell lines. We observed that A375 (but not BLM) cells are able to form melanospheres and show CSCs traits: expression of the pluripotency markers SOX2 and KLF4, higher invasiveness and tumor formation capability in vivo with respect to parental adherent cells. We also showed that a subpopulation of autofluorescent cells expressing the ABCG2 stem cell marker is present in the A375 spheroid culture. Based on these data, we investigated whether δ-TT might target melanoma CSCs. We demonstrated that melanoma cells escaping the antitumor activity of δ-TT are completely devoid of the ability to form melanospheres. In contrast, cells that escaped vemurafenib treatment show a higher ability to form melanospheres than control cells. δ-TT also induced disaggregation of A375 melanospheres and reduced the spheroidogenic ability of sphere-derived cells, reducing the expression of the ABCG2 marker. These data demonstrate that δ-TT exerts its antitumor activity by targeting the CSC subpopulation of A375 melanoma cells and might represent a novel chemopreventive/therapeutic strategy against melanoma.

Indexed as

ATP Binding Cassette Transporter, Subfamily G, Member 2Biomarkers, TumorCell AdhesionCell Line, TumorCell ProliferationCell SurvivalHumansIndolesKruppel-Like Factor 4Kruppel-Like Transcription FactorsMelanomaNeoplasm ProteinsNeoplastic Stem CellsSOXB1 Transcription FactorsSpheroids, CellularSulfonamidesABCG2 protein, humanATP Binding Cassette Transporter, Subfamily G, Member 2Biomarkers, TumorIndolesKLF4 protein, humanKruppel-Like Factor 4Kruppel-Like Transcription FactorsNeoplasm ProteinsSOX2 protein, humanSOXB1 Transcription FactorsSulfonamidestocotrienol, deltaVemurafenibVitamin E

Identifiers

PMID29330434
PMCPMC5766483

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.