Evidence map›Paper›PMID 38465433›Full record

ArticleCurrent cancer drug targets2025

HAND2-AS1 Promotes Ferroptosis to Reverse Lenvatinib Resistance in Hepatocellular Carcinoma by TLR4/NOX2/DUOX2 Axis.

Zheng Song, Yu Zhang, Wei Luo, Chao Sun, Caihong Lv, Sihao Wang, Quanwei He, Ran Xu, Zhaofang Bai, Xiujuan Chang and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Current cancer drug targets, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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  5. Article
  6. Review
  7. Long-term exposure to PMScientific reports · 2024
    Article
  8. Review
  9. Review
  10. Review
  11. Current Progress of Ferroptosis Study in Hepatocellular Carcinoma.International journal of biological sciences · 2024
    Review
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.

Zheng SongPeking University 302 Clinical Medical School, Beijing, China.
Yu ZhangPeking University 302 Clinical Medical School, Beijing, China.
Wei LuoDepartment of Liver Disease of Chinese PLA General Hospital, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Chao SunDepartment of Liver Disease of Chinese PLA General Hospital, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Caihong LvPeking University 302 Clinical Medical School, Beijing, China.
Sihao WangDepartment of Liver Disease of Chinese PLA General Hospital, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Quanwei HeDepartment of Liver Disease of Chinese PLA General Hospital, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Ran XuDepartment of Liver Disease of Chinese PLA General Hospital, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Zhaofang BaiDepartment of Liver Disease of Chinese PLA General Hospital, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Xiujuan ChangDepartment of Liver Disease of Chinese PLA General Hospital, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Yongping YangPeking University 302 Clinical Medical School, Beijing, China.

Funding

Beijing Natural Science Foundation 7212101Research and Translational Application of Clinical Characteristic Diagnosis and Treatment Technology in the Capital Z221100007422002State Key Projects Specialized on Infectious Diseases, Chinese Ministry of Science and Technology 2013ZX10005002, 2018ZX10725506
6 · The paper itself

Abstract

introductionLenvatinib resistance causes less than 40% of the objective response rate. Therefore, it is urgent to explore new therapeutic targets to reverse the lenvatinib resistance for HCC. HAND2-AS1 is a critical tumor suppressor gene in various cancers.

methodsHere, we investigated the role of HAND2-AS1 in the molecular mechanism of lenvatinib resistance in HCC. It was found that HAND2-AS1 was lowly expressed in the HepG2 lenvatinib resistance (HepG2-LR) cells and HCC tissues and associated with progression-free intervals via TCGA. Overexpression of HAND2-AS1 (OE-HAND2-AS1) decreased the IC

resultsA xenograft model in which nude mice were injected with OE-HAND2-AS1 HepG2-LR cells confirmed that OE-HAND2-AS1 could reverse lenvatinib resistance and decrease tumor formation

conclusionHAND2-AS1 promotes ferroptosis in HCC cells and reverses lenvatinib resistance by regulating TLR4/NOX2/DUOX2 axis. It suggested that HAND2-AS1 may be a potential therapeutic target and an indicator of early recurrence for HCC.

Indexed as

Carcinoma, HepatocellularDrug Resistance, NeoplasmFerroptosisLiver NeoplasmsNADPH Oxidase 2Phenylurea CompoundsQuinolinesToll-Like Receptor 4AnimalsFemaleHep G2 CellsHumansMaleMiceMice, Inbred BALB CMice, NudeCYBB protein, humanlenvatinibNADPH Oxidase 2Phenylurea CompoundsQuinolinesTLR4 protein, humanToll-Like Receptor 4cancercellsdeathsHepatocellular carcinomalenvatinib.reactive oxygen species

Identifiers

PMID38465433

What OpenQuestion holds

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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.