Evidence map›Paper›PMID 26684585›Full record

ArticleJournal of biochemistry2016

Characterization of the 5'-flanking region of the human TP53 gene and its response to the natural compound, Resveratrol.

Fumiaki Uchiumi, Koichiro Shoji, Yuki Sasaki, Moe Sasaki, Yamato Sasaki, Takahiro Oyama, Kyoko Sugisawa, Sei-ichi Tanuma

Open access · hybridAbstract read
In one paragraph

Article in Journal of biochemistry, 2016. 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
0.9field-weighted citation impact, top 23% 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, 13 citations in OpenAlex.

  1. Effect of Culture Supernatant ofInternational journal of molecular sciences · 2024
    Article
  2. Induction of the humanMolecular medicine reports · 2024
    Article
  3. Genome-Protecting Compounds as Potential Geroprotectors.International journal of molecular sciences · 2020
    Review
  4. Review
  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

8 authors at 2 institutions in 2 countries.

Fumiaki UchiumiDepartment of Gene Regulation, Faculty of Pharmaceutical Sciences; Research Center for RNA Science, RIST; uchiumi@rs.noda.tus.ac.jp.
Koichiro ShojiDepartment of Gene Regulation, Faculty of Pharmaceutical Sciences;
Yuki SasakiDepartment of Gene Regulation, Faculty of Pharmaceutical Sciences;
Moe SasakiDepartment of Gene Regulation, Faculty of Pharmaceutical Sciences;
Yamato SasakiDepartment of Gene Regulation, Faculty of Pharmaceutical Sciences;
Takahiro OyamaDepartment of Gene Regulation, Faculty of Pharmaceutical Sciences;
Kyoko SugisawaDepartment of Gene Regulation, Faculty of Pharmaceutical Sciences;
Sei-ichi TanumaResearch Center for RNA Science, RIST; Biochemistry, Faculty of Pharmaceutical Sciences; and Drug Creation Frontier Research Center, RIST, Tokyo University of Science, Noda-shi, Chiba-ken 278-8510, Japan.
Immune Regulation (United Kingdom) · GBTokyo University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumour suppressor p53, which is encoded by theTP53gene, is widely known to play an important role in response to DNA damage and various stresses. It has recently been reported that p53 regulates glucose metabolism and that an increase in p53 protein level is induced after serum deprivation or treatments with a natural compound,trans-Resveratrol (Rsv). In this study, we constructed a Luciferase expression vector, pGL4-TP53-551, containing 551 bp of the 5'-upstream region of the humanTP53gene, which was then transfected into HeLa S3 cells. A Luciferase assay showed that Rsv treatment increased the promoter activity of theTP53gene in comparison to that ofPIF1 Detailed deletion and mutation analyses revealed that Nkx-2.5 and E2F-binding elements are required in addition to duplicated GGAA (TTCC), for the regulation ofTP53promoter activity. In this study, it is suggested that the transient induction ofTP53gene expression by Rsv treatment might be partly involved in its anti-aging effect through maintenance of chromosomal DNAs.

Indexed as

5' Flanking RegionPromoter Regions, GeneticAntioxidantsBinding SitesCellular SenescenceDNA HelicasesGene Expression RegulationHeLa CellsHumansLuciferasesMutationResveratrolSequence DeletionStilbenesTumor Suppressor Protein p53AntioxidantsDNA HelicasesLuciferasesPIF1 protein, humanResveratrolStilbenesTP53 protein, humanTumor Suppressor Protein p53E2FETSNkx-2.5ResveratrolTP53

Identifiers

PMID26684585
PMCPMC4885937
OpenAlexW2255901197

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.