Evidence map›Paper›PMID 28424421›Full record

ArticleOncotarget2017

The soy-derived peptide Lunasin inhibits invasive potential of melanoma initiating cells.

Chris Shidal, Jun-Ichi Inaba, Kavitha Yaddanapudi, Keith R Davis

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Lunasin and Its Epigenetic Impact in Cancer Chemoprevention.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Lunasin as a Promising Plant-Derived Peptide for Cancer Therapy.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Liposomes Loaded with Unsaponifiable Matter fromNanomaterials (Basel, Switzerland) · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. MicroRNA-92 Expression in CD133Cancer research · 2019
    Article
  15. Article
  16. 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

4 authors at 3 institutions in 1 country.

Chris ShidalDepartment of Pharmacology and Toxicology, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Jun-Ichi InabaDepartment of Plant Pathology, University of Kentucky, Lexington, Kentucky, USA.
Kavitha YaddanapudiJames Graham Brown Cancer Center, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Keith R DavisDepartment of Biology and Biotechnology Program, Indiana University, Bloomington, Indiana, USA.
University of Louisville · USIndiana University Bloomington · USUniversity of Kentucky · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lunasin is a 44 amino acid peptide with multiple functional domains including an aspartic acid tail, an RGD domain, and a chromatin-binding helical domain. We recently showed that Lunasin induced a phenotype switch of cancer initiating cells (CIC) out of the stem compartment by inducing melanocyte-associated differentiation markers while simultaneously reducing stem-cell-associated transcription factors. In the present study, we advance the hypothesis that Lunasin can reduce pools of melanoma cells with stem cell-like properties, and demonstrate that Lunasin treatment effectively inhibits the invasive potential of CICs in vitro as well as in vivo in a mouse experimental metastasis model. Mice receiving Lunasin treatment had significantly reduced pulmonary colonization after injection of highly metastatic B16-F10 melanoma cells compared to mice in the control group. Mechanistic studies demonstrate that Lunasin reduced activating phosphorylations of the intracellular kinases FAK and AKT as well as reduced histone acetylation of lysine residues in H3 and H4 histones. Using peptides with mutated activity domains, we functionally demonstrated that the RGD domain is necessary for Lunasin uptake and its ability to inhibit oncosphere formation by CICs, thus confirming that Lunasin's ability to affect CICs is at least in part due to the suppression of integrin signaling. Our studies suggest that Lunasin represents a unique anticancer agent that could be developed to help prevent metastasis and patient relapse by reducing the activity of CICs which are known to be resistant to current chemotherapies.

Indexed as

AcetylationAnimalsAntineoplastic Agents, PhytogenicCell Line, TumorExtracellular Signal-Regulated MAP KinasesFocal Adhesion Kinase 1Gene ExpressionHistonesHumansIntegrinsLung NeoplasmsMelanomaMelanoma, ExperimentalMiceNeoplastic Stem CellsPeptidesAntineoplastic Agents, PhytogenicExtracellular Signal-Regulated MAP KinasesFocal Adhesion Kinase 1GM2S-1 protein, soybeanHistonesIntegrinsPeptidesProto-Oncogene Proteins c-aktRetinal DehydrogenaseSoybean Proteinscancer stem cellshistone acetylationintegrin signalingLunasinmelanoma

Identifiers

PMID28424421
PMCPMC5421948
OpenAlexW2591885318

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.