Evidence map›Paper›PMID 31515297›Full record

ArticleMolecular cancer therapeutics2019

Fenretinide, Tocilizumab, and Reparixin Provide Multifaceted Disruption of Oral Squamous Cell Carcinoma Stem Cell Properties: Implications for Tertiary Chemoprevention.

Susan R Mallery, Daren Wang, Brian Santiago, Ping Pei, Caroline Bissonnette, Jayanetti Asiri Jayawardena, Steven P Schwendeman, Richard Spinney, James Lang

Abstract read
In one paragraph

Article in Molecular cancer therapeutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Targeting Sphingolipids for Cancer Therapy.Frontiers in oncology · 2021
    Review
  12. Review
  13. Leukoplakia and Immunology: New Chemoprevention Landscapes?International journal of molecular sciences · 2020
    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

9 authors.

Susan R Mallery *Division of Oral Maxillofacial Pathology and Radiology, College of Dentistry, The Ohio State University, Columbus, Ohio. mallery.1@osu.edu.
Daren Wang *Division of Oral Maxillofacial Pathology and Radiology, College of Dentistry, The Ohio State University, Columbus, Ohio.
Brian SantiagoDivision of Oral Maxillofacial Pathology and Radiology, College of Dentistry, The Ohio State University, Columbus, Ohio.
Ping PeiDivision of Oral Maxillofacial Pathology and Radiology, College of Dentistry, The Ohio State University, Columbus, Ohio.
Caroline BissonnetteDivision of Oral Maxillofacial Pathology and Radiology, College of Dentistry, The Ohio State University, Columbus, Ohio.
Jayanetti Asiri JayawardenaDivision of Oral Maxillofacial Pathology and Radiology, College of Dentistry, The Ohio State University, Columbus, Ohio.
Steven P SchwendemanCollege of Pharmacy, University of Michigan, Ann Arbor, Michigan.
Richard SpinneyDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio.
James LangThe Ohio State University Comprehensive Cancer, Columbus, Ohio.

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Formulation, Evaluation, and Phase 0 Trial of Nanoparticle Releasing Oral Thin Film for OSCC ChemopreventionR01CA258757 · NCI · OHIO STATE UNIVERSITY · PI Susan R Mallery · 2022 to 2026
$3.0M
Assessment of Chemopreventive Effects of a Mucoadhesive Fenretinide Patch on Premalignant Oral Epithelial LesionsR01CA227273 · NCI · OHIO STATE UNIVERSITY · PI MALLERY, SUSAN R · 2019 to 2024
$2.8M
Secondary Chemoprevention of Oral Cancer by Locally Delivered AgentsR01CA211611 · NCI · OHIO STATE UNIVERSITY · PI MALLERY, SUSAN R · 2017 to 2021
$1.8M
Evaluation of locally-delivered fenretinide and black raspberries for oral cancerR01CA171329 · NCI · OHIO STATE UNIVERSITY · PI MALLERY, SUSAN R · 2012 to 2016
$1.6M
NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA171329NCI NIH HHS R01 CA211611NCI NIH HHS R01 CA227273NCI NIH HHS R01 CA258757
6 · The paper itself

Abstract

Locoregional recurrence of oral squamous cell carcinoma (OSCC) dramatically reduces patient survival. Further, as many OSCC recurrences are inoperable, radiotherapy and chemotherapy with or without biological adjuncts are the remaining treatment options. Although the tumors may initially respond, radiotherapy- and chemotherapy-resistant cancer stem cells (CSC) can readily repopulate OSCC tumors. Currently, following the initial OSCC treatment, patients are closely monitored until a recurrence or a second primary is detected. Identification of agents with complementary mechanisms to suppress CSC tumorigenic functions could change this passive approach. The goals of this study were twofold: (1) develop and validate CSC-enriched (CSCE) OSCC cell lines and (2) identify chemopreventive agents that obstruct multiple CSCE protumorigenic pathways. CSCE cultures, which were created by paclitaxel treatment followed by three tumorsphere passes, demonstrated CSC characteristics, including increased expression of stem cell and inflammatory genes, increased aldehyde dehydrogenase (ALDH) activity, and enhanced

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Squamous CellChemopreventionFemaleFenretinideHumansMaleMouth NeoplasmsSulfonamidesTransfectionAntibodies, Monoclonal, HumanizedFenretinidereparixinSulfonamidestocilizumab

Identifiers

PMID31515297
PMCPMC6891199

What OpenQuestion holds

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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.