Evidence map›Paper›PMID 28612196›Full record

ReviewJournal of physiology and biochemistry2016

Cell source, differentiation, functional stimulation, and potential application of human thermogenic adipocytes in vitro.

Dinh-Toi Chu, Yang Tao, Le Hoang Son, Duc-Hau Le

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Journal of physiology and biochemistry, 2016. 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Dinh-Toi ChuInstitute for Research and Development, Duy Tan University, 03 Quang Trung, Da Nang, Vietnam. chudinhtoi.hnue@gmail.com.ORCID http://orcid.org/0000-0002-4596-2022
Yang TaoCollege of Food Science and Technology, Nanjing Agricultural University, Nanjing, Vietnam.
Le Hoang SonVNU University of Science, Vietnam National University, Hanoi, Vietnam.
Duc-Hau LeVINMEC Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam.
Hanoi National University of Education · VNVietnam National University, Hanoi · VNVinmec International Hospital · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent investigations have showed that the functional thermogenic adipocytes are present in both infants and adult humans. Accumulating evidence suggests that the coexistence of classical and inducible brown (brite) adipocytes in humans at adulthood and these adipocytes function to generate heat from energy resulting in reducing body fat and improving glucose metabolism. Human thermogenic adipocytes can be differentiated in vitro from stem cells, cell lines, or adipose stromal vascular fraction. Pre-activated human brite adipocytes in vitro can maintain their thermogenic function in normal or obese immunodeficient mice; therefore, they improve glucose homeostasis and reduce fat mass in obese animals. These key findings have opened a new door to use in vitro thermogenic adipocytes as a cell therapy to prevent obesity and related disorders. Thus, this paper intends to highlight our knowledge in aspects of in vitro human brite/brown adipocytes for the further studies.

Indexed as

AdipocytesAdipose TissueAnimalsCell DifferentiationCell LineHumansInduced Pluripotent Stem CellsObesityStem Cell TransplantationThermogenesisBrown/brite adipocytesBrown/brite adipogenesisHuman thermogenic adipocytes in vitroOverweight and obesityThermogenesis

Identifiers

PMID28612196
OpenAlexW2626851106

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.