Evidence map›Paper›PMID 38243102›Full record

ArticleCell biochemistry and biophysics2024

Adiponectin Receptor Agonist Effectively Suppresses Hepatocellular Carcinoma Growth.

Mai Ly Thi Nguyen, Chi Pham, Van Tran Pham, Phuong Linh Thi Nham, Ba Thang Ta, Dinh Tuan Le, Quoc Vuong Le, Xuan Cuong Hoang, Przemyslaw Bozko, Linh Toan Nguyen and 1 more

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Article in Cell biochemistry and biophysics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Adiponectin Regulated by Indole-3-Acetic Acid in Paneth Cells Controls Renewal and Differentiation of Gut Stem Cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  5. Adipokines: masterminds of metabolic inflammation.Nature reviews. Immunology · 2025
    Review
  6. 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

11 authors at 2 institutions in 2 countries.

Mai Ly Thi NguyenVietnam Military Medical University, Hanoi, Vietnam.
Chi PhamLaboratory Animal Research Centre, Vietnam Military Medical University, Hanoi, Vietnam.
Van Tran PhamVietnam Military Medical University, Hanoi, Vietnam.
Phuong Linh Thi NhamLaboratory Animal Research Centre, Vietnam Military Medical University, Hanoi, Vietnam.
Ba Thang TaVietnam Military Medical University, Hanoi, Vietnam.
Dinh Tuan LeVietnam Military Medical University, Hanoi, Vietnam.
Quoc Vuong LeVietnam Military Medical University, Hanoi, Vietnam.
Xuan Cuong HoangVietnam Military Medical University, Hanoi, Vietnam.
Przemyslaw BozkoDepartment of Internal medicine I, Universitätsklinikum Tübingen, Tübingen, Germany.
Linh Toan NguyenVietnam Military Medical University, Hanoi, Vietnam.
Khac Cuong BuiVietnam Military Medical University, Hanoi, Vietnam. buikhaccuong@gmail.com.ORCID http://orcid.org/0000-0002-5781-5898
Vietnam Military Medical University · VNUniversitätsklinikum Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the second lethal cancer. Short overall survival, low five-year survival rate, and unimproved treatment efficacy urge the need to improve HCC prognosis. Adiponectin is key protector against cancer and hepatic abnormalities. Hypoadiponectinemia occurs in and promotes carcinogenesis and hepatic diseases. Adiponectin reactivation by different methods showed impressive effect against cancer and hepatic diseases. Recently, AdipoRon, an adiponectin receptor agonist, can interact with both Adiponectin receptors. AdipoRon showed promising anti-cancer effect in some cancers, but no study on HCC yet. The in vitro effect of AdipoRon on HCC was investigated by cell viability, migration, invasion, colony formation and apoptosis assays. The signalling alteration was determined by RT-qPCR and Western blot. The effect of treatment was interpreted by comparison between treatments and control. The difference between two cell lines was relatively compared. Our results showed significant in vitro anti-cancer effect of AdipoRon via AMPK- and dose-dependent manner. Huh7 cells showed a lower level of AdipoR1/2 and a superior proliferation and aggressiveness, compared to Hep3B. In addition, Huh7 cells were more sensitive to AdipoRon treatment (lower IC

Indexed as

Carcinoma, HepatocellularCell ProliferationLiver NeoplasmsReceptors, AdiponectinAMP-Activated Protein KinasesApoptosisCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionSignal TransductionAMP-Activated Protein KinasesReceptors, AdiponectinAdiponectinAdipoRonAMPKAnticancerHCCSEMA7A

Identifiers

PMID38243102
OpenAlexW4391042369

What OpenQuestion holds

Textmetadata
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.