Evidence map›Paper›PMID 33801898›Full record

ArticleJournal of clinical medicine2021

Metabolomic Alteration of Oral Keratinocytes and Fibroblasts in Hypoxia.

Hiroko Kato, Masahiro Sugimoto, Ayame Enomoto, Miku Kaneko, Yuko Hara, Naoaki Saito, Aki Shiomi, Hisashi Ohnuki, Kenji Izumi

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  5. 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

9 authors at 3 institutions in 1 country.

Hiroko KatoResearch Center for Advanced Oral Science, School of Medical and Dental Sciences, Niigata University, Nii-gata 951-8514, Japan.ORCID 0000-0002-2618-5539
Masahiro SugimotoResearch and Development Center for Minimally Invasive Therapies, Health Promotion and Preemptive Medicine, Tokyo Medical University, Tokyo 160-8402, Japan.ORCID 0000-0003-3316-2543
Ayame EnomotoInstitute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata 997-0052, Japan.
Miku KanekoInstitute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata 997-0052, Japan.
Yuko HaraDivision of Biomimetics, School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.
Naoaki SaitoDivision of Biomimetics, School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.ORCID 0000-0002-8752-1057
Aki ShiomiDivision of Dental Education Research Development, School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.
Hisashi OhnukiDivision of Biomimetics, School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.
Kenji IzumiDivision of Biomimetics, School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.ORCID 0000-0002-6302-6828
Niigata University · JPKeio University · JPTokyo Medical University · JP

Funding

Japan Society for the Promotion of Science 15K20476Japan Society for the Promotion of Science 17K11800Japan Society for the Promotion of Science 20B205Tsuruoka cityYamagata prefecture
6 · The paper itself

Abstract

The oxygen concentration in normal human tissue under physiologic conditions is lower than the atmospheric oxygen concentration. The more hypoxic condition has been observed in the cells with wound healing and cancer. Somatic stem cells reside in a hypoxic microenvironment in vivo and prefer hypoxic culture conditions in vitro. Oral mucosa contains tissue-specific stem cells, which is an excellent tissue source for regenerative medicine. For clinical usage, maintaining the stem cell in cultured cells is important. We previously reported that hypoxic culture conditions maintained primary oral keratinocytes in an undifferentiated and quiescent state and enhanced their clonogenicity. However, the metabolic mechanism of these cells is unclear. Stem cell biological and pathological findings have shown that metabolic reprogramming is important in hypoxic culture conditions, but there has been no report on oral mucosal keratinocytes and fibroblasts. Herein, we conducted metabolomic analyses of oral mucosal keratinocytes and fibroblasts under hypoxic conditions. Hypoxic oral keratinocytes and fibroblasts showed a drastic change of metabolite concentrations in urea cycle metabolites and polyamine pathways. The changes of metabolic profiles in glycolysis and the pentose phosphate pathway under hypoxic conditions in the oral keratinocytes were consistent with those of other somatic stem cells. The metabolic profiles in oral fibroblasts showed only little changes in any pathway under hypoxia except for a significant increase in the antioxidant 2-oxoglutaric acid. This report firstly provides the holistic changes of various metabolic pathways of hypoxic cultured oral keratinocytes and fibroblasts.

Indexed as

metabolomicsoral fibroblastsoral keratinocytesoxygen biology

Identifiers

PMID33801898
PMCPMC8001958
OpenAlexW3135897070

What OpenQuestion holds

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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.