Evidence map›Paper›PMID 11571533›Full record

ArticleCancer gene therapy2001

Single-chain antibody-mediated gene delivery into ErbB2-positive human breast cancer cells.

X Li, P Stuckert, I Bosch, J D Marks, W A Marasco

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-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

23 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Extracellular Vesicle-MediatedMolecular cancer therapeutics · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. [Construction and verification of anti-MM scFv-tP fusion protein expression vector].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2017
    Article
  9. Review
  10. Article
  11. Article
  12. Applying horizontal gene transfer phenomena to enhance non-viral gene therapy.Journal of controlled release : official journal of the Controlled Release Society · 2013
    Review
  13. Article
  14. scFv antibody: principles and clinical application.Clinical & developmental immunology · 2012
    Review
  15. Review
  16. Article
  17. Article
  18. The role of HER2 in cancer therapy and targeted drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2010
    Review
  19. Epithelial membrane protein-2 is a novel therapeutic target in ovarian cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2010
    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

5 authors at 2 institutions in 1 country.

X LiDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.
P Stuckert
I Bosch
J D Marks
W A Marasco
Dana-Farber Cancer Institute · USUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeted gene transfer by nonviral vectors can be achieved through incorporation of specific ligand(s) into the vectors. In this study, the effects of incorporation of an anti-ErbB2 single-chain antibody fragment (ScFv) into nonviral vectors for targeted gene delivery were investigated. The ML39 ScFv, selected from a human ScFv phage display library and affinity matured in vitro (K(d)=1 x 10(-9) M), was used as ligand specific for the extracellular domain of the tumor surface protein, ErbB2. Two approaches were taken: (a) development of a vector that is composed of a bifunctional fusion protein capable of binding DNA with the ErbB2-specific ML39 ScFv at its N-terminus and a truncated form of human protamine at its C-terminus, and (b) formulation and evaluation of delivery vectors consisting of three independent components including ML39 ScFv, protamine, and cationic lipids. We demonstrate that fusion proteins comprised of the ML39 ScFv and a truncated form of protamine, denoted as ScFv-P-S, can selectively deliver exogenous DNA into ErbB2(+) cells, with an 8- to 10-fold increase in expression levels of the luciferase reporter gene in ErbB2(+) cells as compared to ErbB2(-) cells. In addition, vectors formulated by appropriately mixing DNA, ScFv, protamine, and lipids in vitro could even more efficiently deliver the reporter gene into ErbB2(+) cells with approximately 5-fold increase in gene expression in ErbB2(+) cell as compared to ErbB2(-) cells. Expression and refolding of the ScFv fusion proteins, in addition to determination of optimal conditions for vector development using these approaches, are discussed.

Indexed as

Genetic TherapyAmino Acid SequenceArtificial Gene FusionBinding SitesBreast NeoplasmsFemaleFlow CytometryGene ExpressionGenes, erbB-2Genetic VectorsHumansImmunoglobulin FragmentsLiposomesMolecular Sequence DataPeptide LibraryProtaminesImmunoglobulin Fragmentsimmunoglobulin FvLiposomesPeptide LibraryProtaminesRecombinant Fusion Proteins

Identifiers

PMID11571533
OpenAlexW2001723579

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.