Cited by 210RNA Interference and Gene DeliveryCancer-related Molecular PathwaysCancer-related molecular mechanisms research

The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.

Synthetic small inhibiting RNAs: Efficient tools to inactivate oncogenic mutations and restore p53 pathways

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Martinez, Luis Alfonso, Naguibneva, Irina, Lehrmann, Heike, Vervisch, Arlette, Tchénio, Thierry, Lozano, Guillermina, Harel-Bellan, Annick·2002·Proceedings of the National Academy of Sciences

Abstract

Single base pair mutations that alter the function of tumor suppressor genes and oncogenes occur frequently during oncogenesis. The guardian of the genome, p53, is inactivated by point mutation in more than 50% of human cancers. Synthetic small inhibiting RNAs (siRNAs) can suppress gene expression in mammalian cells, although their degree of selectivity might be compromised by an amplification mechanism. Here, we demonstrate that a single base difference in siRNAs discriminates between mutant and WT p53 in cells expressing both forms, resulting in the restoration of WT protein function. Therefore, siRNAs may be used to suppress expression of point-mutated genes and provide the basis for selective and personalized antitumor therapy.

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  1. Vousden K. H. (2002) Biochim. Biophys. Acta1602,47-59.11960694
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Metadata

Authors
Martinez, L. A., Naguibneva, I., Lehrmann, H., Vervisch, A., Tchénio, T., Lozano, G., & Harel-Bellan, A.
Affiliations
  • Centre National de la Recherche Scientifique (FR)
  • Scripps Research Institute (US)
  • Unité Propre de Recherche 9079, Centre National de la Recherche Scientifique-Ligue Nationale Contre le Cancer, Service de Cytofluorométrie, Unité Propre de Recherche 1983, Centre National de la Recherche Scientifique, Institut André Lwoff, 7 Rue Guy Moquet, 94800 Villejuif, France; and University of Texas M. D. Anderson Cancer Center, Department of Molecular Genetics, Section of Cancer Genetics, 1515 Holcombe Boulevard, Houston, TX 77030
Venue
Proceedings of the National Academy of Sciences
Published
2002-10-28
Volume
99
Issue
23
Pages
14849-14854
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2017991840
Cited by
210
References
40
Citations by year
2026: 1 · 2025: 2 · 2024: 3 · 2023: 3 · 2022: 4 · 2021: 4 · 2020: 3 · 2019: 6 · 2018: 5 · 2017: 7 · 2016: 2 · 2015: 4 · 2014: 6 · 2013: 5 · 2012: 8
FWCI
7.88
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Association pour la Recherche sur le Cancer
  • Philippe Foundation
  • National Cancer Institute (CA09212502)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
  • Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
Keywords
siRNA, p53, point mutations, tumor suppressor, oncogenes, cancer therapy, precision oncology, gene expression inhibition
MeSH terms
Base Sequence, Humans, Mutation, Gene Expression Regulation, Neoplastic, Genes, p53, Tumor Suppressor Protein p53, Point Mutation, RNA, Small Interfering

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