Evidence map›Paper›PMID 20127797›Full record

ArticleStem cells (Dayton, Ohio)2010

A novel molecule integrating therapeutic and diagnostic activities reveals multiple aspects of stem cell-based therapy.

Shawn D Hingtgen, Randa Kasmieh, Jeroen van de Water, Ralph Weissleder, Khalid Shah

Open access · hybridAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 55 citations in OpenAlex.

  1. Cell and gene therapy in neuro-oncology.Handbook of clinical neurology · 2024
    Review
  2. Article
  3. Article
  4. Gene Therapy for High Grade Glioma: The Clinical Experience.Expert opinion on biological therapy · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. The MUDENG Augmentation: A Genesis in Anti-Cancer Therapy?International journal of molecular sciences · 2020
    Review
  10. 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
  11. Developing Implantable Scaffolds to Enhance Neural Stem Cell Therapy for Post-Operative Glioblastoma.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Neural stem cell therapy for cancer.Methods (San Diego, Calif.) · 2016
    Review
  18. Article
  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

5 authors at 4 institutions in 1 country.

Shawn D HingtgenMolecular Neurotherapy and Imaging Laboratory, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, USA.
Randa Kasmieh
Jeroen van de Water
Ralph Weissleder
Khalid Shah
Massachusetts General Hospital · USCenter for Systems Biology · USHarvard Stem Cell Institute · USHarvard University · US

Funding

In vivo imaging and therapeutic efficacy of NSC-secreted nanobodiesR21CA131980 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI SHAH, KHALID A · 2008 to 2009
$434k
NCI NIH HHS R21 CA131980NCI NIH HHS R21CA131980
6 · The paper itself

Abstract

Stem cells are promising therapeutic delivery vehicles; however pre-clinical and clinical applications of stem cell-based therapy would benefit significantly from the ability to simultaneously determine therapeutic efficacy and pharmacokinetics of therapies delivered by engineered stem cells. In this study, we engineered and screened numerous fusion variants that contained therapeutic (TRAIL) and diagnostic (luciferase) domains designed to allow simultaneous investigation of multiple events in stem cell-based therapy in vivo. When various stem cell lines were engineered with the optimized molecule, SRL(O)L(2)TR, diagnostic imaging showed marked differences in the levels and duration of secretion between stem cell lines, while the therapeutic activity of the molecule showed the different secretion levels translated to significant variability in tumor cell killing. In vivo, simultaneous diagnostic and therapeutic monitoring revealed that stem cell-based delivery significantly improved pharmacokinetics and anti-tumor effectiveness of the therapy compared to intravenous or intratumoral delivery. As treatment for highly malignant brain tumor xenografts, tracking SRL(O)L(2)TR showed stable stem cell-mediated delivery significantly regressed peripheral and intracranial tumors. Together, the integrated diagnostic and therapeutic properties of SRL(O)L(2)TR answer critical questions necessary for successful utilization of stem cells as novel therapeutic vehicles.

Indexed as

Genes, ReporterStem Cell TransplantationAnimalsApoptosisCell LineCoculture TechniquesGenetic TherapyGlioblastomaHumansMiceXenograft Model Antitumor Assays

Identifiers

PMID20127797
PMCPMC3021283
OpenAlexW1966369003

What OpenQuestion holds

Textmetadata
LicenceTDM
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.