Evidence map›Paper›PMID 33457002›Full record

ArticleJournal of gastrointestinal oncology2020

High expression of the

Zai-Yi Fei, Wei-Si Wang, Su-Fen Li, Jia-Ji Zi, Li Yang, Ting Liu, Song Ao, Qian-Qian Liu, Qing-Hua Cui, Min Yu and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of gastrointestinal oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 36% 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.

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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

11 authors at 2 institutions in 1 country.

Zai-Yi FeiSchool of Life Sciences, Yunnan University, Kunming, China.
Wei-Si WangCollege of Basic Medical Sciences, Dali University, Dali, China.
Su-Fen LiCollege of Basic Medical Sciences, Dali University, Dali, China.
Jia-Ji ZiCollege of Basic Medical Sciences, Dali University, Dali, China.
Li YangSchool of Life Sciences, Yunnan University, Kunming, China.
Ting LiuSchool of Life Sciences, Yunnan University, Kunming, China.
Song AoSchool of Life Sciences, Yunnan University, Kunming, China.
Qian-Qian LiuSchool of Life Sciences, Yunnan University, Kunming, China.
Qing-Hua CuiSchool of Life Sciences, Yunnan University, Kunming, China.
Min YuSchool of Life Sciences, Yunnan University, Kunming, China.
Wei XiongCollege of Basic Medical Sciences, Dali University, Dali, China.
Yunnan University · CNDali University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMitochondrial transcription elongation factor (TEFM) is an essential molecule that regulates the replication-transcription switch of mitochondrial DNA. TEFM modulates both transcription elongation and RNA processing in mitochondria. The purpose of the present study was to determine the association of TEFM with tumor progression and prognosis in hepatocellular carcinoma (HCC) patients.

methodsThe different protein expression level of TEFM among HCC cell lines was detected by Western blotting. The gene expression profiling interactive analysis (GEPIA) was used to dynamically analyze the mRNA expression of

resultsTEFM is upregulated in HCC cell lines compared to noncancerous liver cell line. TEFM protein and mRNA expression levels in HCC tissues were significantly upregulated compared with those in noncancerous liver tissues. In addition, the mRNA expression level of TEFM was significantly correlated with sex, serum AFP level, and vascular invasion (P<0.05). Further analysis showed that high expression level of TEFM was unfavorable in terms of the prognosis of patients with HCC. Cox multivariate regression analysis showed that patient age, vascular invasion, and TEFM expression were independent factors affecting the prognosis of HCC patients (P<0.05). The expression level of the TEFM gene was significantly positively correlated with the expression of multiple mitochondrial regulatory genes and biomarker genes of HCC (P<0.01, R>0).

conclusionsOur findings reveal that TEFM may play an important role in the progression of HCC. More importantly, the elevated expression of TEFM may potentially predict poor overall survival (OS) and disease-free survival (DFS) in patients with HCC.

Indexed as

hepatocellular carcinoma (HCC)immunohistochemistryMitochondrial transcription elongation factor (TEFM)prognosisTCGA dataset

Identifiers

PMID33457002
PMCPMC7807266
OpenAlexW3109334830

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.