Evidence map›Paper›PMID 28179988›Full record

ArticleCell death discovery2017

iPS-derived MSCs from an expandable bank to deliver a prodrug-converting enzyme that limits growth and metastases of human breast cancers.

M Ullah, Y Kuroda, T J Bartosh, F Liu, Q Zhao, C Gregory, R Reger, J Xu, R H Lee, D J Prockop

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2017. 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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. SAR-CoV-2 infection, emerging new variants and the role of activation induced cytidine deaminase (AID) in lasting immunity.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2021
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Clinical Relevance of RNA Editing to Early Detection of Cancer in Human.International journal of stem cell research and therapy · 2020
    Article
  12. Review
  13. Article
  14. The Dynamic Roles of Mesenchymal Stem Cells in Colon Cancer.Canadian journal of gastroenterology & hepatology · 2018
    Review
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

M UllahInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
Y KurodaInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
T J BartoshInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
F LiuInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
Q ZhaoInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
C GregoryInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
R RegerInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
J XuInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
R H LeeInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
D J ProckopInstitute for Regenerative Medicine at Scott & White, Texas A&M University and Health Science Center, College of Medicine , Temple, TX 76502, USA.
Texas A&M University System · US

Funding

Preparation and Distribution of Adult Stem CellsP40OD011050 · OD · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI PROCKOP, DARWIN JOHNSON · 2012 to 2017
$6.0M
NIH HHS P40 OD011050
6 · The paper itself

Abstract

One attractive strategy to treat cancers is to deliver an exogenous enzyme that will convert a non-toxic compound to a highly toxic derivative. The strategy was tested with viral vectors but was disappointing because the efficiency of transduction into tumor cells was too low. Recent reports demonstrated that the limitation can be addressed by using tissue-derived mesenchymal stromal cells (MSCs) to deliver enzyme/prodrug systems that kill adjacent cancer cells through bystander effects. Here we addressed the limitation that tissue-derived MSCs vary in their properties and are difficult to generate in the large numbers needed for clinical applications. We prepared a Feeder Stock of MSCs from induced pluripotent stem cells (iPSs) that provided an extensively expandable source of standardized cells. We then transduced the iPS-derived MSCs to express cytosine deaminase and injected them locally into a mouse xenogeneic model of human breast cancer. After administration of the prodrug (5-fluorocytosine), the transduced iPS-MSCs both limited growth of preformed tumors and decreased lung metastases.

Identifiers

PMID28179988
PMCPMC5292869
OpenAlexW2587214604

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.