Evidence map›Paper›PMID 32517377›Full record

ArticlePharmaceutics2020

Resveratrol Enhances mRNA and siRNA Lipid Nanoparticles Primary CLL Cell Transfection.

Edo Kon, Inbal Hazan-Halevy, Daniel Rosenblum, Niv Cohen, Sushmita Chatterjee, Nuphar Veiga, Pia Raanani, Osnat Bairey, Ohad Benjamini, Arnon Nagler and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Endosomal escape: A bottleneck for LNP-mediated therapeutics.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Microfluidic technologies and devices for lipid nanoparticle-based RNA delivery.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Review
  9. Review
  10. Review
  11. Review
  12. 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

11 authors at 3 institutions in 1 country.

Edo KonLaboratory of Precision NanoMedicine, Tel Aviv University, Tel Aviv 69978, Israel.
Inbal Hazan-HalevyLaboratory of Precision NanoMedicine, Tel Aviv University, Tel Aviv 69978, Israel.
Daniel RosenblumLaboratory of Precision NanoMedicine, Tel Aviv University, Tel Aviv 69978, Israel.
Niv CohenLaboratory of Precision NanoMedicine, Tel Aviv University, Tel Aviv 69978, Israel.
Sushmita ChatterjeeLaboratory of Precision NanoMedicine, Tel Aviv University, Tel Aviv 69978, Israel.
Nuphar VeigaLaboratory of Precision NanoMedicine, Tel Aviv University, Tel Aviv 69978, Israel.
Pia RaananiDavidoff Cancer Center, Beilinson Hospital, Rabin Medical Center Petah Tiqva, Institute of Hematology, Petah Tikva 49100, Israel.
Osnat BaireyDavidoff Cancer Center, Beilinson Hospital, Rabin Medical Center Petah Tiqva, Institute of Hematology, Petah Tikva 49100, Israel.
Ohad BenjaminiChaim Sheba Medical Center, Tel-Hashomer, Ramat Gan 52621, Israel.
Arnon NaglerChaim Sheba Medical Center, Tel-Hashomer, Ramat Gan 52621, Israel.
Dan PeerLaboratory of Precision NanoMedicine, Tel Aviv University, Tel Aviv 69978, Israel.
Tel Aviv University · ILRabin Medical Center · ILSheba Medical Center · IL

Funding

Varda and Boaz Dotan Research Center for Hemato-Oncology Research, Tel Aviv University 2016/11
6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) is the most common adult leukemia in Western populations. Therapies such as mRNA and siRNA encapsulated in lipid nanoparticles (LNPs) represent a clinically advanced platform and are utilized for a wide variety of applications. Unfortunately, transfection of RNA into CLL cells remains a formidable challenge and a bottleneck for developing targeted therapies for this disease. Therefore, we aimed to elucidate the barriers to efficient transfection of RNA-encapsulated LNPs into primary CLL cells to advance therapies in the future. To this end, we transfected primary CLL patient samples with mRNA and siRNA payloads encapsulated in an FDA-approved LNP formulation and characterized the transfection. Additionally, we tested the potential of repurposing caffeic acid, curcumin and resveratrol to enhance the transfection of nucleic acids into CLL cells. The results demonstrate that the rapid uptake of LNPs is required for successful transfection. Furthermore, we demonstrate that resveratrol enhances the delivery of both mRNA and siRNA encapsulated in LNPs into primary CLL patient samples, overcoming inter-patient heterogeneity. This study points out the important challenges to consider for efficient RNA therapeutics for CLL patients and advocates the use of resveratrol in combination with RNA lipid nanoparticles to enhance delivery into CLL cells.

Indexed as

B lymphocytecaffeic acidcliniccurcumindrug deliveryendosomal escapeRNA therapies

Identifiers

PMID32517377
PMCPMC7355647
OpenAlexW3033538576

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.