Evidence map›Paper›PMID 18369324›Full record

ReviewGene therapy2008

Stem and progenitor cell-mediated tumor selective gene therapy.

K S Aboody, J Najbauer, M K Danks

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Gene therapy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 136 papers.

0numbers the graph read from it
0cells of the map it votes in
136citing papers in PubMed
18.3field-weighted citation impact, top 1% 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

136 citing papers in PubMed, 272 citations in OpenAlex.

  1. Review
  2. Review
  3. Auto-loaded TRAIL-exosomes derived from induced neural stem cells for brain cancer therapy.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Nerves in gastrointestinal cancer: from mechanism to modulations.Nature reviews. Gastroenterology & hepatology · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Cancer and stem cells.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  14. Article
  15. The Potentials and Pitfalls of Using Adult Stem Cells in Cancer Treatment.Advances in experimental medicine and biology · 2021
    Review
  16. Review
  17. Article
  18. Generation and Profiling of Tumor-Homing Induced Neural Stem Cells from the Skin of Cancer Patients.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  19. Review
  20. Article

76 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

K S AboodyDivision of Hematology/Hematopoietic Cell Transplantation, City of Hope National Medical Center and Beckman Research Institute, Duarte, CA, USA. kaboody@coh.org
J Najbauer
M K Danks
City Of Hope National Medical Center · USSt. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
SELECTIVE THERAPY OF NEUROBLASTOMAR01CA079763 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DANKS, MARY K · 1999 to 2007
$1.7M
SELECTIVE THERAPY OF TUMORS THAT OVEREXPRESS C MYCR01CA076202 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI POTTER, PHILIP M · 1998 to 2006
$1.6M
Neural Progenitor Cells as Cancer Therapy VectorsR01CA113446 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI ABOODY, KAREN S · 2005 to 2009
$1.5M
NCI NIH HHS CA113446NCI NIH HHS CA21765NCI NIH HHS CA76202NCI NIH HHS CA79763NCI NIH HHS R01 CA113446
6 · The paper itself

Abstract

The poor prognosis for patients with aggressive or metastatic tumors and the toxic side effects of currently available treatments necessitate the development of more effective tumor-selective therapies. Stem/progenitor cells display inherent tumor-tropic properties that can be exploited for targeted delivery of anticancer genes to invasive and metastatic tumors. Therapeutic genes that have been inserted into stem cells and delivered to tumors with high selectivity include prodrug-activating enzymes (cytosine deaminase, carboxylesterase, thymidine kinase), interleukins (IL-2, IL-4, IL-12, IL-23), interferon-beta, apoptosis-promoting genes (tumor necrosis factor-related apoptosis-inducing ligand) and metalloproteinases (PEX). We and others have demonstrated that neural and mesenchymal stem cells can deliver therapeutic genes to elicit a significant antitumor response in animal models of intracranial glioma, medulloblastoma, melanoma brain metastasis, disseminated neuroblastoma and breast cancer lung metastasis. Most studies reported reduction in tumor volume (up to 90%) and increased survival of tumor-bearing animals. Complete cures have also been achieved (90% disease-free survival for >1 year of mice bearing disseminated neuroblastoma tumors). As we learn more about the biology of stem cells and the molecular mechanisms that mediate their tumor-tropism and we identify efficacious gene products for specific tumor types, the clinical utility of cell-based delivery strategies becomes increasingly evident.

Indexed as

AnimalsCell LineGenetic EngineeringGenetic TherapyGene Transfer TechniquesHumansMesenchymal Stem CellsMesenchymal Stem Cell TransplantationNeoplasmsStem Cells

Identifiers

PMID18369324
OpenAlexW2148278891

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.