Evidence map›Paper›PMID 16144874›Full record

ArticleStem cells (Dayton, Ohio)2005

Bypass of senescence, immortalization, and transformation of human hematopoietic progenitor cells.

Sergey S Akimov, Ali Ramezani, Teresa S Hawley, Robert G Hawley

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.3field-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

22 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Non-invasiveOncotarget · 2017
    Article
  7. Fluorescent Proteins for Flow Cytometry.Current protocols in cytometry · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Stable gammaretroviral vector expression during embryonic stem cell-derived in vitro hematopoietic development.Molecular therapy : the journal of the American Society of Gene Therapy · 2006
    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

4 authors at 2 institutions in 1 country.

Sergey S AkimovDepartment of Anatomy and Cell Biology, The George Washington University Medical Center, 2300 I Street NW, Washington, DC 20037, USA.
Ali Ramezani
Teresa S Hawley
Robert G Hawley
Washington University Medical Center · USGeorge Washington University · US

Funding

Molecular Chimerism Therapy for Hemophilia AR01HL065519 · NHLBI · GEORGE WASHINGTON UNIVERSITY · PI HAWLEY, ROBERT G. · 2001 to 2009
$3.0M
IMPROVED LENTIVIRAL VECTORS FOR PRIMATE ES CELLSR24RR016209 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI THOMSON, JAMES ALEXANDER · 2002 to 2006
$2.2M
Embryoid Body-derived Hematopoietic Stem Cell LinesR01HL066305 · NHLBI · GEORGE WASHINGTON UNIVERSITY · PI HAWLEY, ROBERT G. · 2001 to 2005
$1.7M
NCRR NIH HHS R24 RR016209NCRR NIH HHS R24RR16209NHLBI NIH HHS R01 HL065519NHLBI NIH HHS R01 HL066305NHLBI NIH HHS R01HL65519NHLBI NIH HHS R01HL66305
6 · The paper itself

Abstract

We attempted to extend the lifespan of CD34+ stem/progenitor cells in human cord blood (CB) by transduction with lentiviral vectors carrying the human telomerase catalytic subunit (hTERT) and/or the human papillomavirus type 16 (HPV16) E6 and E7 oncogenes. We found that hTERT was incapable of prolonging the replicative capacity of CB cells maintained under serum-free conditions in the presence of stem cell factor, Flt3 ligand, thrombopoietin, and interleukin-3 beyond 4 months (n=3). However, transduced CB cells cultured in the same cytokine cocktail constitutively expressing HPV16 E6/E7 alone (n=2) or in concert with hTERT (n=9) continued to proliferate, giving rise to permanent (>2 years) cell lines with a CD45+ CD34- CD133+/- CD44+ CD235a+ CD71+ CD203+ CD33+ CD13+ myeloerythroid/mast cell progenitor phenotype. Notably, CB cell cultures expressing only HPV16 E6/E7 went through a crisis period, and the resulting oligoclonal cell lines were highly aneuploid. By comparison, the CB cell lines obtained by coexpression of HPV16 E6/E7 plus hTERT exhibited near-diploid karyotypes with minimal chromosomal aberrations, concomitant with stabilization of telomere length, yet were clonally derived. The immortalized E6/E7 plus hTERT-expressing CB cells were not tumorigenic when injected intravenously or subcutaneously into sublethally irradiated immunodeficient nonobese diabetic/severe combined immunodeficient mice but could be converted to a malignant state by ectopic expression of a v-H-ras or BCR-ABL oncogene. These findings provide new insights into the mechanisms governing the senescence checkpoint of primitive human hematopoietic precursors and establish a paradigm for studies of the multistep process of human leukemogenesis.

Indexed as

Antigens, CD34Cell Line, TransformedCell Transformation, ViralCellular SenescenceDNA-Binding ProteinsFetal BloodGenetic VectorsHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHIV-1HumansLentivirusOncogene Proteins, ViralPapillomavirus E7 ProteinsRepressor ProteinsStem CellsAntigens, CD34DNA-Binding ProteinsE6 protein, Human papillomavirus type 16oncogene protein E7, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus E7 ProteinsRepressor ProteinsTelomerase

Identifiers

PMID16144874
PMCPMC1360608
OpenAlexW2027434466

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.