Evidence map›Paper›PMID 24382340›Full record

ReviewFertility and sterility2014

Adult somatic cells to the rescue: nuclear reprogramming and the dispensability of gonadal germ cells.

Charles A Easley, David R Latov, Calvin R Simerly, Gerald Schatten

Abstract readReview
In one paragraph

Review in Fertility and sterility, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. 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.

Charles A EasleyLaboratory of Translational Cell Biology, Department of Cell Biology, Emory University School of Medicine, Atlanta, Georgia.
David R LatovLaboratory of Translational Cell Biology, Department of Cell Biology, Emory University School of Medicine, Atlanta, Georgia.
Calvin R SimerlyDepartment of Obstetrics, Gynecology, & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Magee Womens Research Institute, Pittsburgh Development Center, Pittsburgh, Pennsylvania.
Gerald SchattenDepartment of Obstetrics, Gynecology, & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; Magee Womens Research Institute, Pittsburgh Development Center, Pittsburgh, Pennsylvania. Electronic address: schattengp@upmc.edu.
Emory University · USUniversity of Pittsburgh · US

Funding

Frontiers in Alzheimer's and Aging Research (FrA2R)R25AG043365 · NIA · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI GERALD SCHATTEN · 2012 to 2026
$5.8M
Frontiers in Stem Cells in Cancer(FriSC2)R25CA163168 · NCI · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI SCHATTEN, GERALD · 2011 to 2020
$3.1M
Rehabilitative and Regenerative Medicine for Minority Health & Health DisparitiesT15HD072833 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI SCHATTEN, GERALD · 2012 to 2014
$390k
NCI NIH HHS R25 CA163168NIA NIH HHS R25 AG043365NICHD NIH HHS T15 HD072833
6 · The paper itself

Abstract

With advances in cancer therapies, survival rates in prepubescent patients have steadily increased. However, a number of these surviving patients have been rendered sterile owing to their rigorous oncologic treatment regimens. In addition to cancer treatments, men and women, who are genetically fertile, can become infertile owing to immune suppression treatments, exposure to environmental and industrial toxicants, and injury. Notwithstanding the great emotional burden from an inability to conceive a child with their partner, the financial burdens for testing and treatment are high, and successful treatment of these patients' sterility is rare. Recent advances in pluripotent stem cell differentiation and the generation of patient-specific, induced pluripotent stem cells indicate that stem cell replacement therapies or in vitro differentiation followed by IVF may be on the horizon. Here we discuss these recent advances, their relevance to treating male-factor and female-factor infertility, and what experimental procedures must be carried out in animal models before these exciting new treatments can be used in a clinical setting. The goal of this research is to generate functional gametes from no greater starting material than a mere skin biopsy.

Indexed as

Adult Stem CellsAnimalsCellular ReprogrammingFemaleGerm CellsGonadsHumansInfertilityMalePluripotent Stem CellsStem Cell Transplantationassisted reproductive technologydifferentiationInfertilitystem cells

Identifiers

PMID24382340
PMCPMC4285723
OpenAlexW2123285282

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.