Evidence map›Paper›PMID 33355244›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

VLA4-Targeted Nanoparticles Hijack Cell Adhesion-Mediated Drug Resistance to Target Refractory Myeloma Cells and Prolong Survival.

Francesca Fontana, Michael J Scott, John S Allen, Xiaoxia Yang, Grace Cui, Dipanjan Pan, Noriko Yanaba, Mark A Fiala, Julie O'Neal, Anne H Schmieder-Atteberry and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Recent advances in targeted drug delivery systems for multiple myeloma.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Review
  9. Review
  10. Review
  11. Targeting integrin pathways: mechanisms and advances in therapy.Signal transduction and targeted therapy · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Cancer drug resistance in multiple myeloma.Cancer drug resistance (Alhambra, Calif.) · 2022
    Article
  20. 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

17 authors at 4 institutions in 1 country.

Francesca FontanaDivision of Cardiology, Washington University School of Medicine, St. Louis, Missouri. greg.lanza@mac.com francesca.fontana@wustl.edu.
Michael J ScottDivision of Cardiology, Washington University School of Medicine, St. Louis, Missouri.
John S AllenDivision of Cardiology, Washington University School of Medicine, St. Louis, Missouri.
Xiaoxia YangDivision of Cardiology, Washington University School of Medicine, St. Louis, Missouri.
Grace CuiDivision of Cardiology, Washington University School of Medicine, St. Louis, Missouri.
Dipanjan PanUniversity of Maryland, Baltimore County, University of Maryland School of Medicine, Baltimore, Maryland.
Noriko YanabaDivision of Cardiology, Washington University School of Medicine, St. Louis, Missouri.
Mark A FialaDivison of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0002-0208-5023
Julie O'NealDivison of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
Anne H Schmieder-AtteberryDivision of Cardiology, Washington University School of Medicine, St. Louis, Missouri.
Julie RitcheyDivison of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
Michael RettigDivison of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
Kathleen SimonsSUNY Downstate Health Sciences University, New York, New York.
Steven FletcherUniversity of Maryland School of Pharmacy, Baltimore, Maryland.
Ravi VijDivison of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
John F DiPersioDivison of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
Gregory M LanzaDivision of Cardiology, Washington University School of Medicine, St. Louis, Missouri. greg.lanza@mac.com francesca.fontana@wustl.edu.
Washington University in St. Louis · USSUNY Downstate Health Sciences University · USUniversity of Maryland, Baltimore · USUniversity of Maryland, Baltimore County · US

Funding

Project 2 - Radiation-Induced Treatment of Multiple Myeloma using NanoparticlesU54CA199092 · NCI · WASHINGTON UNIVERSITY · PI ACHILEFU, SAMUEL, LANZA, GREGORY M · 2015 to 2019
$11.5M
Resource Based Center for Musculoskeletal Biology and Medicine (Overall Application)P30AR074992 · NIAMS · WASHINGTON UNIVERSITY · PI MATTHEW J SILVA · 2019 to 2026
$6.8M
OVERCOMING THE PROTECTIVE BARRIERS OF BREAST CANCER IN BONE MARROW WITH TARGETED PRODRUG NANOTHERAPYR01CA216840 · NCI · WASHINGTON UNIVERSITY · PI LANZA, GREGORY M, WEILBAECHER, KATHERINE NELSON · 2018 to 2022
$3.1M
NEXT GENERATION APPROACHES TO BREAST CANCER USING IMAGE GUIDED DRUG DELIVERYR01CA154737 · NCI · WASHINGTON UNIVERSITY · PI LANZA, GREGORY M, PAN, DIPANJAN · 2011 to 2015
$2.4M
BM NICHE DISRUPTION AND IMMUNOTHERAPY IN HEMATOLOGICAL MALIGNANCIESR50CA211466 · NCI · WASHINGTON UNIVERSITY · PI Michael Rettig · 2016 to 2026
$2.3M
NCI NIH HHS R01 CA154737NCI NIH HHS R01 CA216840NCI NIH HHS R50 CA211466NCI NIH HHS U54 CA199092NIAMS NIH HHS P30 AR074992
6 · The paper itself

Abstract

purposeIn multiple myeloma, drug-resistant cells underlie relapse or progression following chemotherapy. Cell adhesion-mediated drug resistance (CAM-DR) is an established mechanism used by myeloma cells (MMC) to survive chemotherapy and its markers are upregulated in residual disease. The integrin very late antigen 4 (VLA4; α EXPERIMENTAL

designWe synthetized 20 nm VLA4-targeted micellar nanoparticles (V-NP) carrying DiI for tracing or a novel camptothecin prodrug (V-CP). Human or murine MMCs, alone or with stroma, and immunocompetent mice with orthotopic multiple myeloma were used to track delivery of NPs and response to treatments.

resultsV-NPs selectively delivered their payload to MMCs

conclusionsV-CP may be a safe and effective strategy to prevent or treat relapsing or refractory myeloma. V-NP targeting of resistant cells may suggest a new approach to environment-induced resistance in cancer.

Indexed as

AnimalsCamptothecinCell AdhesionCell Line, TumorDexamethasoneDrug Resistance, NeoplasmHumansIntegrin alpha4beta1MelphalanMiceMice, Inbred C57BLMultiple MyelomaNanoparticlesTopoisomerase I InhibitorsCamptothecinDexamethasoneIntegrin alpha4beta1MelphalanTopoisomerase I Inhibitors

Identifiers

PMID33355244
PMCPMC8026499
OpenAlexW3115993039

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.