Evidence map›Paper›PMID 24877058›Full record

ReviewBioMed research international2014

Involvement of DNA damage response pathways in hepatocellular carcinoma.

Sheau-Fang Yang, Chien-Wei Chang, Ren-Jie Wei, Yow-Ling Shiue, Shen-Nien Wang, Yao-Tsung Yeh

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

63 citing papers in PubMed, 101 citations in OpenAlex.

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3 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 1 country.

Sheau-Fang YangDepartment of Pathology, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung City 801, Taiwan ; Department of Pathology, Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung City 807, Taiwan.
Chien-Wei ChangDepartment of Medical Laboratory Sciences and Biotechnology, Fooyin University, Kaohsiung City 831, Taiwan ; Cancer Center and Division of General & Gastroenterological Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.ORCID 0000-0003-3177-2567
Ren-Jie WeiDepartment of Medical Laboratory Sciences and Biotechnology, Fooyin University, Kaohsiung City 831, Taiwan ; Department of Pathology, Kaohsiung Armed Forces General Hospital, Kaohsiung City 802, Taiwan ; Department of Biological Sciences, National Sun Yat-sen University, Kaohsiung City 804, Taiwan.
Yow-Ling ShiueDepartment of Biological Sciences, National Sun Yat-sen University, Kaohsiung City 804, Taiwan.
Shen-Nien WangDepartment of Surgery, Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung City 807, Taiwan ; Division of Hepato-Pancreatico-Biliary Surgery, Kaohsiung Medical University Hospital, Kaohsiung City 807, Taiwan.
Yao-Tsung YehDepartment of Medical Laboratory Sciences and Biotechnology, Fooyin University, Kaohsiung City 831, Taiwan.ORCID 0000-0002-7780-7983
Kaohsiung Medical University · TWNational Sun Yat-sen University · TWFooyin University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) has been known as one of the most lethal human malignancies, due to the difficulty of early detection, chemoresistance, and radioresistance, and is characterized by active angiogenesis and metastasis, which account for rapid recurrence and poor survival. Its development has been closely associated with multiple risk factors, including hepatitis B and C virus infection, alcohol consumption, obesity, and diet contamination. Genetic alterations and genomic instability, probably resulted from unrepaired DNA lesions, are increasingly recognized as a common feature of human HCC. Dysregulation of DNA damage repair and signaling to cell cycle checkpoints, known as the DNA damage response (DDR), is associated with a predisposition to cancer and affects responses to DNA-damaging anticancer therapy. It has been demonstrated that various HCC-associated risk factors are able to promote DNA damages, formation of DNA adducts, and chromosomal aberrations. Hence, alterations in the DDR pathways may accumulate these lesions to trigger hepatocarcinogenesis and also to facilitate advanced HCC progression. This review collects some of the most known information about the link between HCC-associated risk factors and DDR pathways in HCC. Hopefully, the review will remind the researchers and clinicians of further characterizing and validating the roles of these DDR pathways in HCC.

Indexed as

DNA DamageAnimalsCarcinoma, HepatocellularCell Cycle CheckpointsChromosome AberrationsDNA AdductsHumansLiver NeoplasmsSignal TransductionDNA Adducts

Identifiers

PMID24877058
PMCPMC4022277
OpenAlexW2055528768

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.