Evidence map›Paper›PMID 20507312›Full record

ArticleBritish journal of haematology2010

All trans retinoic acid nanodisks enhance retinoic acid receptor mediated apoptosis and cell cycle arrest in mantle cell lymphoma.

Amareshwar T K Singh, Andrew M Evens, Reilly J Anderson, Jennifer A Beckstead, Natesan Sankar, Antonella Sassano, Savita Bhalla, Shuo Yang, Leonidas C Platanias, Trudy M Forte and 2 more

Abstract read
In one paragraph

Article in British journal of haematology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Reconstituted HDL as a therapeutic delivery device.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2021
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  13. High-Density Lipoproteins for Therapeutic Delivery Systems.Journal of materials chemistry. B · 2016
    Article
  14. Article
  15. Review
  16. Review
  17. Cationic lipid nanodisks as an siRNA delivery vehicle.Biochemistry and cell biology = Biochimie et biologie cellulaire · 2014
    Article
  18. Review
  19. Article
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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 3 institutions in 1 country.

Amareshwar T K SinghDivision of Haematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA. a-singh@northwestern.edu
Andrew M Evens
Reilly J Anderson
Jennifer A Beckstead
Natesan Sankar
Antonella Sassano
Savita Bhalla
Shuo Yang
Leonidas C Platanias
Trudy M Forte
Robert O Ryan
Leo I Gordon
Robert H. Lurie Comprehensive Cancer Center of Northwestern UniversityJesse Brown VA Medical Center · USNorthwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Targeting Novel Protein Complexes for the Treatment of Acute Myeloid LeukemiaR01CA121192 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PLATANIAS, LEONIDAS C. · 2006 to 2023
$4.1M
Effect of Apolipoprotein Structural AdaptabilityR37HL064159 · NHLBI · UNIVERSITY OF NEVADA RENO · PI RYAN, ROBERT O'MARA · 2010 to 2019
$4.1M
EFFECT OF APOLIPOPROTEIN STRUCTURAL ADAPTABILITYR01HL064159 · NHLBI · CHILDREN'S HOSPITAL &RES CTR AT OAKLAND · PI RYAN, ROBERT O'MARA · 2000 to 2009
$3.6M
Nanobiotechnology for the Treatment of Mantle Cell LymphomaR43CA141904 · NCI · LYPRO BIOSCIENCES, INC. · PI FORTE, TRUDY M · 2009 to 2009
$109k
NCI NIH HHS 1R43CA141904NCI NIH HHS CA121192NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA121192NCI NIH HHS R43 CA141904NHLBI NIH HHS HL-64159NHLBI NIH HHS R01 HL064159NHLBI NIH HHS R37 HL064159
6 · The paper itself

Abstract

Mantle cell lymphoma (MCL) is characterized by translocation t(11;14)(q13;q32), aggressive clinical behaviour, and poor patient outcomes following conventional chemotherapy. New treatment approaches are needed that target novel biological pathways. All trans retinoic acid (ATRA) is a key retinoid that acts through nuclear receptors that function as ligand-inducible transcription factors. The present study evaluated cell killing effects of ATRA-enriched nanoscale delivery particles, termed nanodisks (ND), on MCL cell lines. Results show that ATRA-ND induced cell death more effectively than naked ATRA (dimethyl sulphoxide) or empty ND. ATRA-ND induced reactive oxygen species (ROS) generation to a greater extent than naked ATRA. The antioxidant, N-acetylcysteine, inhibited ATRA-ND induced apoptosis. Compared to naked ATRA, ATRA-ND enhanced G1 growth arrest, up-regulated p21and p27, and down regulated cyclin D1. At ATRA concentrations that induced apoptosis, expression levels of retinoic acid receptor-alpha (RARalpha) and retinoid X receptor-gamma (RXRgamma) were increased. Compared to naked ATRA, ATRA-ND significantly stimulated transcriptional activity of RARA in a model carcinoma cell line. Furthermore, the RAR antagonist, Ro 41-5253, inhibited ATRA-ND induced ROS generation and prevented ATRA-ND induced cell growth arrest and apoptosis. In summary, incorporation of ATRA into ND enhanced the biological activity of this retinoid in cell culture models of MCL.

Indexed as

Antineoplastic AgentsApoptosisBenzoatesCell CycleCell Cycle ProteinsChromansDrug Delivery SystemsDrug Evaluation, PreclinicalGuanine Nucleotide Exchange FactorsHumansLymphoma, Mantle-CellNanoparticlesNeoplasm ProteinsNuclear ProteinsReactive Oxygen SpeciesReceptors, Retinoic AcidAntineoplastic AgentsBenzoatesCell Cycle ProteinsChromansGuanine Nucleotide Exchange FactorsNeoplasm ProteinsNuclear ProteinsRCC1 protein, humanReactive Oxygen SpeciesReceptors, Retinoic AcidRetinoid X ReceptorsRo 41-5253Tretinoin

Identifiers

PMID20507312
PMCPMC2907750
OpenAlexW1706952306

What OpenQuestion holds

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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.