Evidence map›Paper›PMID 25045589›Full record

ArticleJournal of stem cell research & therapy2013

Safeguarding Stem Cell-Based Regenerative Therapy against Iatrogenic Cancerogenesis: Transgenic Expression of

Marek Malecki, Christine LaVanne, Dominique Alhambra, Chaitanya Dodivenaka, Sarah Nagel, Raf Malecki

Abstract read
In one paragraph

Article in Journal of stem cell research & therapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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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

6 authors at 1 institution in 1 country.

Marek MaleckiPhoenix Biomolecular Engineering Foundation, San Francisco, CA 94105, USA ; University of Wisconsin, Madison, WI 53706, USA.
Christine LaVanneUniversity of Wisconsin, Madison, WI 53706, USA.
Dominique AlhambraUniversity of Wisconsin, Madison, WI 53706, USA.
Chaitanya DodivenakaSouth Dakota State University, Brookings, SD 57007, USA.
Sarah NagelSouth Dakota State University, Brookings, SD 57007, USA.
Raf MaleckiPhoenix Biomolecular Engineering Foundation, San Francisco, CA 94105, USA ; San Francisco State University, San Francisco, CA 94123, USA.
University of Wisconsin Foundation · US

Funding

WATER DISTRIB:PHYSICAL PROPERT:PIZZA &LMPS MOZZARELLA CHEESES:EARLY STAGE MATURP41RR002301 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI MARKLEY, JOHN LUTE · 1985 to 2011
$13.0M
XENOPUS OOCYTE NUCLEAR ENVELOPE STRUCTUREP41RR000570 · NCRR · UNIVERSITY OF WISCONSIN MADISON · 1985 to 1998
–
NCRR NIH HHS P41 RR000570NCRR NIH HHS P41 RR002301
6 · The paper itself

Abstract

introductionThe worst possible complication of using stem cells for regenerative therapy is iatrogenic cancerogenesis. The ultimate goal of our work is to develop a self-triggering feedback mechanism aimed at causing death of all stem cells, which resist directed differentiation, keep proliferating, and can grow into tumors. SPECIFIC

aimThe specific aim was threefold: (1) to genetically engineer the DNA constructs for the human, recombinant

methodsThe DNA constructs for the human, recombinant

resultsDifferentiation of the pluripotent induced stem cells into the endothelial cells was verified by highlighting formation of tight and adherens junctions through transgenic expression of recombinant fluorescent fusion proteins: VE cadherin, claudin, zona occludens 1, and catenin. Proliferation of the stem cells was determined through highlighting transgenic expression of recombinant fluorescent proteins controlled by

conclusionHerein, we describe attaining the proof-of-concept for the strategy, whereby transgenic expression of the genetically engineered human recombinant DNases in proliferating and directed differentiation resisting stem cells leads to their death. This novel strategy reduces the risk of iatrogenic neoplasms in stem cell therapy.

Indexed as

CancerogenesisDNA polymeraseDNaseNeoplasmPluripotent stem cellRegenerative medicineStage specific embryonal antigenStem cell induced cancerogenesisStem cell therapyTumorigenesis

Identifiers

PMID25045589
PMCPMC4103669
OpenAlexW243253638

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.