Evidence map›Paper›PMID 29855544›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2018

Critical role of deoxynucleotidyl transferase terminal interacting protein 1 in oral cancer.

Yuki Sawai, Atsushi Kasamatsu, Dai Nakashima, Kazuaki Fushimi, Hiroki Kasama, Manabu Iyoda, Yukinao Kouzu, Masashi Shiiba, Hideki Tanzawa, Katsuhiro Uzawa

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  6. Pharmacogenomics and personalized medicine · 2022
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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

10 authors at 5 institutions in 1 country.

Yuki SawaiDepartment of Oral Science, Graduate School of Medicine, Chiba University, Chiba, Japan.
Atsushi KasamatsuDepartment of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan. kasamatsua@faculty.chiba-u.jp.
Dai NakashimaDepartment of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan.
Kazuaki FushimiDepartment of Dentistry and Oral Surgery, Eastern Chiba Medical Center, Chiba, Japan.
Hiroki KasamaDepartment of Dentistry and Oral Surgery, Eastern Chiba Medical Center, Chiba, Japan.
Manabu IyodaDivision of Oral Surgery, Chiba Rosai Hospital, Chiba, Japan.
Yukinao KouzuDivision of Dentistry, Chiba Children's Hospital, Chiba, Japan.
Masashi ShiibaDepartment of Medical Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Hideki TanzawaDepartment of Oral Science, Graduate School of Medicine, Chiba University, Chiba, Japan.
Katsuhiro UzawaDepartment of Oral Science, Graduate School of Medicine, Chiba University, Chiba, Japan. uzawak@faculty.chiba-u.jp.
Chiba University · JPChiba University Hospital · JPTeikyo University Chiba Medical Center · JPChiba Hospital · JPChiba Rosai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deoxynucleotidyl transferase terminal interacting protein 1 (DNTTIP1) forms a complex with histone deacetylase (HDAC); however, the relevance of DNTTIP1 in cancer remains unknown. The aim of this study was to examine DNTTIP1 expression and its functional mechanisms in oral squamous cell carcinomas (OSCCs). DNTTIP1 expression was analyzed by quantitative reverse transcriptase-polymerase chain reaction, immunoblotting analysis, and immunohistochemistry. The expression of DNTTIP1 was upregulated significantly in vitro and in vivo, and in patients with OSCC in whom DNTTIP1 was overexpressed and the expression level was correlated significantly (P < 0.05) with tumoral growth. DNTTIP1 knockdown (siDNTTIP1) cells showed depressed cellular proliferation by cell-cycle arrest at the G1 phase with high acetylation of p53 and upregulation of p21

Indexed as

AgedAnimalsAntineoplastic Agents, PhytogenicCarcinoma, Squamous CellCarrier ProteinsCell Cycle CheckpointsCell Line, TumorCell ProliferationDNA-Binding ProteinsFemaleGene Expression Regulation, NeoplasticHumansMaleMice, Inbred BALB CMice, NudeMouth NeoplasmsAntineoplastic Agents, PhytogenicCarrier ProteinsDNA-Binding ProteinsDNTTIP1 protein, humanNuclear ProteinsResveratrolTranscription Factors

Identifiers

PMID29855544
OpenAlexW2807466035

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.