Evidence map›Paper›PMID 32282912›Full record

ArticleNucleic acids research2020

Selective targeting of mutually exclusive DNA G-quadruplexes: HIV-1 LTR as paradigmatic model.

Martina Tassinari, Michela Zuffo, Matteo Nadai, Valentina Pirota, Adriana Carolina Sevilla Montalvo, Filippo Doria, Mauro Freccero, Sara N Richter

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.5field-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

31 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Rational Polyligand Design for G-Quadruplex Multimer Stabilization.Journal of chemical information and modeling · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Light-Activated Molecules Targeting G-Quadruplex Nucleic Acids.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Combating multidrug-resistance inNAR molecular medicine · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

8 authors at 2 institutions in 1 country.

Martina TassinariDepartment of Molecular Medicine, University of Padova, via A. Gabelli 63, 35121 Padova, Italy.
Michela ZuffoDepartment of Chemistry, University of Pavia, v. le Taramelli 10, 27100, Pavia, Italy.
Matteo NadaiDepartment of Molecular Medicine, University of Padova, via A. Gabelli 63, 35121 Padova, Italy.
Valentina PirotaDepartment of Chemistry, University of Pavia, v. le Taramelli 10, 27100, Pavia, Italy.
Adriana Carolina Sevilla MontalvoDepartment of Chemistry, University of Pavia, v. le Taramelli 10, 27100, Pavia, Italy.
Filippo DoriaDepartment of Chemistry, University of Pavia, v. le Taramelli 10, 27100, Pavia, Italy.
Mauro FrecceroDepartment of Chemistry, University of Pavia, v. le Taramelli 10, 27100, Pavia, Italy.
Sara N RichterDepartment of Molecular Medicine, University of Padova, via A. Gabelli 63, 35121 Padova, Italy.
University of Pavia · ITUniversity of Padua · IT

Funding

European Research Council 615879
6 · The paper itself

Abstract

Targeting of G-quadruplexes, non-canonical conformations that form in G-rich regions of nucleic acids, has been proposed as a novel therapeutic strategy toward several diseases, including cancer and infections. The unavailability of highly selective molecules targeting a G-quadruplex of choice has hampered relevant applications. Herein, we describe a novel approach, based on naphthalene diimide (NDI)-peptide nucleic acid (PNA) conjugates, taking advantage of the cooperative interaction of the NDI with the G-quadruplex structure and hybridization of the PNA with the flanking region upstream or downstream the targeted G-quadruplex. By biophysical and biomolecular assays, we show that the NDI-PNA conjugates are able to specifically recognize the G-quadruplex of choice within the HIV-1 LTR region, consisting of overlapping and therefore mutually exclusive G-quadruplexes. Additionally, the conjugates can induce and stabilize the least populated G-quadruplex at the expenses of the more stable ones. The general and straightforward design and synthesis, which readily apply to any G4 target of choice, together with both the red-fluorescent emission and the possibility to introduce cellular localization signals, make the novel conjugates available to selectively control G-quadruplex folding over a wide range of applications.

Indexed as

G-QuadruplexesHIV Long Terminal RepeatDNAHeLa CellsHIV-1HumansImidesLigandsModels, GeneticNaphthalenesPeptide Nucleic AcidsDNAImidesLigandsnaphthalenediimideNaphthalenesPeptide Nucleic Acids

Identifiers

PMID32282912
PMCPMC7229848
OpenAlexW3015867517

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.