Evidence map›Paper›PMID 29989289›Full record

ReviewCancer science2018

Unveiling epigenetic regulation in cancer, aging, and rejuvenation with in vivo reprogramming technology.

Yuko Sogabe, Hiroshi Seno, Takuya Yamamoto, Yasuhiro Yamada

Open access · goldAbstract readReview
In one paragraph

Review in Cancer science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. LncRNAInternational journal of molecular sciences · 2021
    Review
  7. Review
  8. Review
  9. Review
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.

Yuko SogabeDepartment of Life Science Frontiers, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
Hiroshi SenoDepartment of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Takuya YamamotoDepartment of Life Science Frontiers, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
Yasuhiro YamadaAMED-CREST, AMED, Tokyo, Japan.ORCID http://orcid.org/0000-0002-2463-1478
Kyoto University · JPJapan Agency for Medical Research and Development · JP

Funding

Core Center for iPS Cell ResearchiPS Cell Research FundJapan Agency for Medical Research and Development AMED-CREST, JP18gm0610017Japan Agency for Medical Research and Development AMED-CREST, JP18gm1110004Japan Agency for Medical Research and Development P-CREATE, JP18cm0106203h0003Japan Society for the Promotion of Science (KAKENHI 18H04026)Naito FoundationResearch Center Network for Realization of Regenerative MedicineTakeda Science Foundation
6 · The paper itself

Abstract

Reprogramming technology has enabled the fate conversion of terminally differentiated somatic cells into pluripotent stem cells or into another differentiated state. A dynamic reorganization of epigenetic regulation takes place during cellular reprogramming. Given that reprogramming does not require changes in the underlying genome, the technology can be used to actively modify epigenetic regulation. Although reprogramming has been investigated mostly at the cellular level in vitro, studies have reported that somatic cells are reprogrammable in multicellular organisms in vivo. In vivo reprogramming provides a potential strategy for regenerative medicine. Notably, recent studies using in vivo reprogramming technology to alter epigenetic regulation at organismal levels have revealed unappreciated epigenetic mechanisms in various biological phenomena, including cancer development, tissue regeneration, aging, and rejuvenation in mammals. Moreover, in vivo reprogramming technology can be applied to abrogate epigenetic aberrations associated with aging and cancer, which raises the possibility that the technology could provide a potential strategy to control the fate of detrimental cells such as senescent cells and cancer cells in vivo. Here, we review recent progress and future perspectives of in vivo reprogramming.

Indexed as

AgingCellular ReprogrammingCellular SenescenceDNA MethylationEpigenesis, GeneticHistonesHumansInduced Pluripotent Stem CellsNeoplasmsRegenerationRejuvenationHistonesagingcancercellular senescenceepigeneticsin vivo reprogrammingreprogramming technology

Identifiers

PMID29989289
PMCPMC6125454
OpenAlexW2832351469

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.