Evidence map›Paper›PMID 33222332›Full record

ArticleCancer science2021

NQO1 promotes an aggressive phenotype in hepatocellular carcinoma via amplifying ERK-NRF2 signaling.

Yun Yang, Jie Zheng, Mengchao Wang, Jin Zhang, Tao Tian, Zhiheng Wang, Shengxian Yuan, Lei Liu, Peng Zhu, Fangming Gu and 4 more

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Cancer science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

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  14. The Potential Key Role of the NRF2/NQO1 Pathway in the Health Effects of Arsenic Pollution on SCC.International journal of environmental research and public health · 2022
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4 · The record

Corrections and comments

  • Retraction · 2023-05-22Objections by Third Party · Original Data and/or Images not Provided and/or not Available · Unreliable Results and/or Conclusions ·
  • Retracted
5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Yun YangThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Jie ZhengDepartment of Intervention, First Affiliated Hospital, Wenzhou Medical University, Zhejiang, China.
Mengchao WangThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.ORCID https://orcid.org/0000-0002-6409-4267
Jin ZhangThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Tao TianThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Zhiheng WangThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Shengxian YuanThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Lei LiuThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Peng ZhuThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Fangming GuThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Siyuan FuThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Yunfeng ShanDepartment of Hepatobiliary Surgery, First Affiliated Hospital, Wenzhou Medical University, Zhejiang, China.
Zeya PanThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Weiping ZhouThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Shanghai, China.
Second Military Medical University · CNWenzhou Medical University · CNMinistry of Education of the People's Republic of China · CN

Funding

National Human Genetic Resources Sharing Service Platform 2005DKA21300National Natural Science Foundation of China 81502416National Natural Science Foundation of China 81572791Science Fund for Creative Research Groups, NSFC, China 81521091Shanghai Municipal Commission of Health and Family Planning Project 201440443State Key Infection Disease Project of China 2018ZX10732202-002-005
6 · The paper itself

Abstract

Patients with hepatocellular carcinoma (HCC) are usually diagnosed at the later stages and have poor survival outcomes. New molecules are urgently needed for the prognostic predication and individual treatment. Our study showed that high levels of NQO1 expression frequently exist in HCC with an obvious cancer-specific pattern. Patients with NQO1-high tumors are significantly associated with poor survival outcomes and serve as independent predictors. Functional experiments showed that NQO1 promotes the growth and aggressiveness of HCC in both in vitro and in vivo models, and the underlying mechanism involved NQO1-derived amplification of ERK/p38-NRF2 signaling. Combined block of ERK and NRF2 signaling generated stronger growth inhibition compared with any single block, especially for HCC with high-NQO1. Therefore, NQO1 is a potential biomarker for HCC early diagnosis and prognosis prediction, and also attractive for cancer-specific targets for HCC treatment.

Indexed as

AnimalsBiomarkers, TumorCarcinoma, HepatocellularFemaleHeterograftsHumansLiver NeoplasmsMaleMAP Kinase Signaling SystemMiceMice, Inbred BALB CMice, NudeNAD(P)H Dehydrogenase (Quinone)NF-E2-Related Factor 2PhenotypePrognosisBiomarkers, TumorNAD(P)H Dehydrogenase (Quinone)NFE2L2 protein, humanNF-E2-Related Factor 2NQO1 protein, humanhepatocellular carcinomaNQO1NRF2prognosistumorigenesis

Identifiers

PMID33222332
PMCPMC7894015
OpenAlexW3110331866

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.