Evidence map›Paper›PMID 28924544›Full record

ArticleBalkan journal of medical genetics : BJMG2017

Analysis of the Mitochondrial 4977 Bp Deletion in Patients with Hepatocellular Carcinoma.

Z S Guo, C L Jin, Z J Yao, Y M Wang, B T Xu

Abstract read
In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Article
  7. Article
  8. Mitochondrial dysfunction, UPRCell & bioscience · 2021
    Review
  9. Review
  10. Article
  11. mtDNA deletions responsible for unsuccessful pregnancy after in- vitro fertilization.International journal of reproductive biomedicine · 2020
    Article
  12. Article
  13. Role of the mitochondrial stress response in human cancer progression.Experimental biology and medicine (Maywood, N.J.) · 2020
    Review
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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

5 authors.

Z S GuoDepartment of Hepatobiliary Surgery, Zhuji People's Hospital, Shaoxing, People's Republic of China.
C L JinDepartment of Endocrinology, Zhuji People's Hospital, Shaoxing, People's Republic of China.
Z J YaoDepartment of Hepatobiliary Surgery, Zhuji People's Hospital, Shaoxing, People's Republic of China.
Y M WangDepartment of Hepatobiliary Surgery, Zhuji People's Hospital, Shaoxing, People's Republic of China.
B T XuDepartment of Cardiothoracic Surgery, Zhuji People's Hospital, Shaoxing, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the mitochondrial (mt) genome that result in mt dysfunction, have long been proposed to play important roles in the pathogenesis of hepatocellular carcinoma (HCC). Among these, the common mtDNA 4977 bp deletion is one of the most frequent mutations observed in various cancers. To understand the relationship between the mtDNA 4977 bp deletion and HCC, we performed mutational screening for the presence of this deletion in 105 HCC patients and 69 unrelated healthy subjects. After nested-polymerase chain reaction (nested-PCR) amplification, we found that there were 10 patients carrying the mtDNA 4977 bp deletion, and this deletion was absent in control subjects. Moreover, HCC patients carrying this deletion showed a marked increase in reactive oxygen species (ROS) level and mtDNA copy number when compared with the healthy controls. Taken together, our data indicated that the mtDNA 4977 bp deletion may play important role in the carcinogenesis of HCC, possibly

Indexed as

4977 bp deletionCopy numberHepatocellular carcinoma (HCC)Mitochondrial DNA (mtDNA)reactive oxygen species (ROS)

Identifiers

PMID28924544
PMCPMC5596825

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Registered trials

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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.