Evidence map›Paper›PMID 28685058›Full record

ArticleBiomedical reports2017

Cell division cycle 34 is highly expressed in hepatitis C virus-positive hepatocellular carcinoma with favorable phenotypes.

Keiko Takagi, Tadatoshi Takayama, Yutaka Midorikawa, Hiromasa Hasegawa, Takanaga Ochiai, Masamichi Moriguchi, Tokio Higaki, Masayoshi Soma, Hiroki Nagase, Kyoko Fujiwara

Open access · bronzeAbstract read
In one paragraph

Article in Biomedical reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 3 institutions in 1 country.

Keiko TakagiDepartment of Digestive Surgery, Nihon University School of Medicine, Itabashi, Tokyo 173-8610, Japan.
Tadatoshi TakayamaDepartment of Digestive Surgery, Nihon University School of Medicine, Itabashi, Tokyo 173-8610, Japan.
Yutaka MidorikawaDepartment of Digestive Surgery, Nihon University School of Medicine, Itabashi, Tokyo 173-8610, Japan.
Hiromasa HasegawaDepartment of Oral Pathology, Matsumoto Dental University, Shiojiri, Nagano 399-0781, Japan.
Takanaga OchiaiDepartment of Oral Pathology, Matsumoto Dental University, Shiojiri, Nagano 399-0781, Japan.
Masamichi MoriguchiDepartment of Digestive Surgery, Nihon University School of Medicine, Itabashi, Tokyo 173-8610, Japan.
Tokio HigakiDepartment of Digestive Surgery, Nihon University School of Medicine, Itabashi, Tokyo 173-8610, Japan.
Masayoshi SomaDepartment of General Medicine, Nihon University School of Medicine, Itabashi, Tokyo 173-8610, Japan.
Hiroki NagaseLaboratory of Cancer Genetics, Chiba Cancer Center Research Institute, Chiba 260-8717, Japan.
Kyoko FujiwaraDepartment of General Medicine, Nihon University School of Medicine, Itabashi, Tokyo 173-8610, Japan.
Nihon University · JPMatsumoto Dental University · JPChiba Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite tremendous efforts to develop curative agents, there are few effective drugs for the treatment of hepatocellular carcinoma (HCC). This is predominantly due to the variations in individual HCC cases. As numerous HCC cases have no mutations in known tumor-associated genes, identification of novel genes involved in the development and progression of human cancers is considered to be an urgent issue. In the present study, surgical specimens of HCC were analyzed for the expression patterns of ubiquitin-conjugating enzyme, cell division cycle 34 (CDC34), which is hypomethylated in its promoter region and exhibits elevated expression levels in mouse skin tumors. The results of the current study clearly indicated that the elevated CDC34 expression level in cancerous regions was significantly associated with favorable clinicopathological features, such as reduced alanine aminotransferase (ALT) levels and histological grades. Similarly, a higher T/N ratio, which is the ratio of CDC34 expression in HCCs to that in non-tumorous tissues, was significantly associated with favorable features, such as a lower indocyanin green retention rate after 15 min (ICG15R), reduced α-fetoprotein and smaller tumor size. These results indicate that the CDC34 expression level in HCC is a marker for predicting the HCC prognosis and that CDC34 acts as a tumor suppressor.

Indexed as

cell division cycle 34clinicopathological featurehepatitis C virus-positive hepatocellular carcinomaprognostic markertumor suppressor

Identifiers

PMID28685058
PMCPMC5492648
OpenAlexW2614897476

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.