Evidence map›Paper›PMID 38757223›Full record

ArticleZoological research2024

Overexpression of wild-type HRAS drives non-alcoholic steatohepatitis to hepatocellular carcinoma in mice.

Chen Ling, Su-Su Liu, Yu-Ya Wang, Gui-Tao Huo, Yan-Wei Yang, Nan Xu, Hong Wang, Yong Wu, Yu-Fa Miao, Rui Fu and 2 more

Abstract read
In one paragraph

Article in Zoological research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 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

12 authors.

Chen LingCollege of Life Sciences, Northwest University, Provincial Key Laboratory of Biotechnology of Shaanxi Province, Xi'an, Shaanxi 710069, China.
Su-Su LiuDivision of Animal Model Research, Institute for Laboratory Animal Resources, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, China.
Yu-Ya WangDivision of Animal Model Research, Institute for Laboratory Animal Resources, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, China.
Gui-Tao HuoNational Center for Safety Evaluation of Drugs, National Institutes for Food and Drug Control (NIFDC), Beijing 100176, China.
Yan-Wei YangNational Center for Safety Evaluation of Drugs, National Institutes for Food and Drug Control (NIFDC), Beijing 100176, China.
Nan XuDivision of HIV/AIDS and Sexually Transmitted Virus Vaccines, Institute for Biological Products Control, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, China.
Hong WangDivision of Laboratory Animal Monitoring, Institute for Laboratory Animal Resources, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, China.
Yong WuDivision of Animal Model Research, Institute for Laboratory Animal Resources, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, China.
Yu-Fa MiaoNational Center for Safety Evaluation of Drugs, National Institutes for Food and Drug Control (NIFDC), Beijing 100176, China.
Rui FuDivision of Laboratory Animal Monitoring, Institute for Laboratory Animal Resources, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, China.
Yu-Wei ZhaoCollege of Life Sciences, Northwest University, Provincial Key Laboratory of Biotechnology of Shaanxi Province, Xi'an, Shaanxi 710069, China. E-mail: zhaoyw@nwu.edu.cn.
Chang-Fa FanDivision of Animal Model Research, Institute for Laboratory Animal Resources, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, China. E-mail: fancf@nifdc.org.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC), a prevalent solid carcinoma of significant concern, is an aggressive and often fatal disease with increasing global incidence rates and poor therapeutic outcomes. The etiology and pathological progression of non-alcoholic steatohepatitis (NASH)-related HCC is multifactorial and multistage. However, no single animal model can accurately mimic the full NASH-related HCC pathological progression, posing considerable challenges to transition and mechanistic studies. Herein, a novel conditional inducible wild-type human

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsNon-alcoholic Fatty Liver DiseaseProto-Oncogene Proteins p21(ras)AnimalsDisease Models, AnimalHumansMiceMice, Inbred C57BLMice, TransgenicProto-Oncogene Proteins p21(ras)CirrhosisFibrosisHCCHCC driver factorHRASNASHTHBS1Treatment evaluation

Identifiers

PMID38757223
PMCPMC11188599

What OpenQuestion holds

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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.