Evidence map›Paper›PMID 35853969›Full record

ArticleScientific reports2022

Analysis of mutations in DNA damage repair pathway gene in Chinese patients with hepatocellular carcinoma.

Jiarong Li, Nianfeng Li, Muhammad Salman Azhar, Ling Liu, Liheng Wang, Qi Zhang, Langqing Sheng, Jianhua Wang, Sijia Feng, Qixuan Qiu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. 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

11 authors at 2 institutions in 1 country.

Jiarong LiDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Nianfeng LiDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Muhammad Salman AzharDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Ling LiuDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Liheng WangDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Qi ZhangDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Langqing ShengDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Jianhua WangDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Sijia FengDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Qixuan QiuDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
Yao XiaoDepartment of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China. yaoxiao@csu.edu.cn.
Xiangya Hospital Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence of hepatocellular carcinoma (HCC) has increased in these years. DNA damage repair (DDR) pathway is required in response to DNA damage Gene mutations in DDR pathway play an important role in different stages of tumorigenesis and development. Based on the importance of DDR pathway in precision therapy of multiple cancers, we analyzed DDR gene mutations in Chinese patients with HCC. The results showed that (tumor mutation burden) TMB was significantly higher in HCC patients who carried somatic mutations in DDR than in non-carriers, and TMB in patients with DS, MMR mutations and DDR genes mutations such as RAD50, MLH1, MSH2, CHEK2 was significantly higher than that in wild-type patients. Based on the results of next-generation sequencing (NGS) testing, we are trying to provide clues for targeted therapy and provide feasible basis for PD-1/PD-L1 immune checkpoint inhibitor therapy.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsBiomarkers, TumorChinaDNA DamageDNA RepairHumansMutationBiomarkers, Tumor

Identifiers

PMID35853969
PMCPMC9296649
OpenAlexW4285794481

What OpenQuestion holds

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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.