Evidence map›Paper›PMID 26170308›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Human anti-nucleolin recombinant immunoagent for cancer therapy.

Dario Palmieri, Timothy Richmond, Claudia Piovan, Tyler Sheetz, Nicola Zanesi, Fulvia Troise, Cindy James, Dorothee Wernicke, Fata Nyei, Timothy J Gordon and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Click-constructed modular signal aptamer chimeras enable receptor-independent degradation of membrane proteins.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Advances in aptamer-based nuclear imaging.European journal of nuclear medicine and molecular imaging · 2022
    Review
  15. Fast detection, a precise and sensitive diagnostic agent for breast cancer.Journal of experimental & clinical cancer research : CR · 2022
    Article
  16. Article
  17. Article
  18. Review
  19. 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

16 authors at 2 institutions in 2 countries.

Dario PalmieriDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
Timothy RichmondDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
Claudia PiovanDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
Tyler SheetzDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
Nicola ZanesiDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
Fulvia TroiseCentro di Ingegneria Genetica (CEINGE) Biotecnologie Avanzate, 80145 Naples, Italy;
Cindy JamesDepartment of Mass Spectroscopy and Proteomics, The Ohio State University, Columbus, OH 43210;
Dorothee WernickeDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
Fata NyeiDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
Timothy J GordonDepartment of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210;
Jessica ConsiglioDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
Francesco SalvatoreCentro di Ingegneria Genetica (CEINGE) Biotecnologie Avanzate, 80145 Naples, Italy;
Vincenzo CoppolaDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
Flavia PichiorriDepartment of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210;
Claudia De LorenzoCentro di Ingegneria Genetica (CEINGE) Biotecnologie Avanzate, 80145 Naples, Italy; Department of Molecular Medicine and Medical Biotechnologies, University of Napoli "Federico II", 80131 Naples, Italy carlo.croce@osumc.edu cladelor@unina.it.
Carlo M CroceDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210; carlo.croce@osumc.edu cladelor@unina.it.
The Ohio State University · USUniversity of Naples Federico II · IT

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Tissue CoreP01CA081534 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KIPPS, THOMAS J · 2000 to 2016
$59.5M
Identifying non-coding RNAs for early detection and prevention of lung cancerU01CA166905 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M, PASS, HARVEY IRA · 2013 to 2017
$4.5M
MiRNAs/UCRs: biomarkers for cancer risk, tumor detection, progression & treatmentU01CA152758 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M · 2010 to 2014
$1.8M
Intramural NIH HHSNCI NIH HHS P01 CA081534NCI NIH HHS P30 CA016058NCI NIH HHS U01 CA152758NCI NIH HHS U01CA152758NCI NIH HHS U01 CA166905NCI NIH HHS U01CA166905
6 · The paper itself

Abstract

Nucleolin (NCL) is a nucleocytoplasmic protein involved in many biological processes, such as ribosomal assembly, rRNA processing, and mRNA stabilization. NCL also regulates the biogenesis of specific microRNAs (miRNAs) involved in tumor development and aggressiveness. Interestingly, NCL is expressed on the surface of actively proliferating cancer cells, but not on their normal counterparts. Therefore, NCL is an attractive target for antineoplastic treatments. Taking advantage of phage-display technology, we engineered a fully human single-chain fragment variable, named 4LB5. This immunoagent binds NCL on the cell surface, it is translocated into the cytoplasm of target cells, and it abrogates the biogenesis of NCL-dependent miRNAs. Binding of 4LB5 to NCL on the cell surface of a variety of breast cancer and hepatocellular carcinoma cell lines, but not to normal-like MCF-10a breast cells, dramatically reduces cancer cell viability and proliferation. Finally, in orthotopic breast cancer mouse models, 4LB5 administration results in a significant reduction of the tumor volume without evident side effects. In summary, here we describe, to our knowledge, the first anti-NCL single-chain fragment variable displaying antineoplastic activity against established solid tumors, which could represent the prototype of novel immune-based NCL-targeting drugs with clinical potential as diagnostic and therapeutic tools in a wide variety of human cancers.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCarcinoma, HepatocellularCell Line, TumorCell MembraneCell MovementCell ProliferationCell SurvivalCytoplasmEnzyme-Linked Immunosorbent AssayFemaleHumansLiver NeoplasmsMiceMice, SCIDAntineoplastic AgentsNucleolinPeptide LibraryPhosphoproteinsRecombinant ProteinsRNA-Binding ProteinsSingle-Chain Antibodiescancer immunotherapymicroRNAnucleolinphage-displayscFv

Identifiers

PMID26170308
PMCPMC4522807
OpenAlexW2152122711

What OpenQuestion holds

Textmetadata
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.