Evidence map›Paper›PMID 25051362›Full record

ArticleOncotarget2014

Adiponectin promotes pancreatic cancer progression by inhibiting apoptosis via the activation of AMPK/Sirt1/PGC-1α signaling.

Bingqing Huang, Xixi Cheng, Dan Wang, Meiyu Peng, Zhenyi Xue, Yurong Da, Ning Zhang, Zhi Yao, Min Li, Aimin Xu and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
8.8field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. The role of AMPK in pancreatic cancer: from carcinogenesis to treatment.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  10. The critical role of Sirt1 in ischemic stroke.Frontiers in pharmacology · 2025
    Review
  11. Review
  12. Article
  13. Electro-Metabolic Coupling of Cumulus-Oocyte Complex.International journal of molecular sciences · 2024
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. ∆nFGF1 ProtectsOxidative medicine and cellular longevity · 2022
    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 3 institutions in 3 countries.

Bingqing HuangResearch Center of Basic Medical Science, Tianjin Medical University, Tianjin, China. Key Laboratory of Immune Microenvironment and Diseases of Educational Ministry of China, Department of Immunology, Basic Medical College, Tianjin Medical University, Tianjin, China. These authors contributed equally to this work.
Xixi ChengResearch Center of Basic Medical Science, Tianjin Medical University, Tianjin, China. These authors contributed equally to this work.
Dan WangResearch Center of Basic Medical Science, Tianjin Medical University, Tianjin, China. These authors contributed equally to this work.
Meiyu PengResearch Center of Basic Medical Science, Tianjin Medical University, Tianjin, China.
Zhenyi XueResearch Center of Basic Medical Science, Tianjin Medical University, Tianjin, China.
Yurong DaResearch Center of Basic Medical Science, Tianjin Medical University, Tianjin, China.
Ning ZhangResearch Center of Basic Medical Science, Tianjin Medical University, Tianjin, China.
Zhi YaoKey Laboratory of Immune Microenvironment and Diseases of Educational Ministry of China, Department of Immunology, Basic Medical College, Tianjin Medical University, Tianjin, China.
Min LiDepartment of Integrative Biology & Pharmacology, The University of Texas Medical School at Houston, Houston, TX, USA.
Aimin XuState Key laboratory of Pharmaceutical Biotechnology, and Department of Medicine, University of Hong Kong, Hong Kong, China.
Rongxin ZhangResearch Center of Basic Medical Science, Tianjin Medical University, Tianjin, China. Key Laboratory of Immune Microenvironment and Diseases of Educational Ministry of China, Department of Immunology, Basic Medical College, Tianjin Medical University, Tianjin, China.
Tianjin Medical University · CNThe University of Texas Health Science Center at Houston · USUniversity of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adiponectin is an adipocyte-secreted adipokine with pleiotropic actions. Clinical evidence has shown that serum adiponectin levels are increased and that adiponectin can protect pancreatic beta cells against apoptosis, which suggests that adiponectin may play an anti-apoptotic role in pancreatic cancer (PC). Here, we investigated the effects of adiponectin on PC development and elucidated the underlying molecular mechanisms. Adiponectin deficiency markedly attenuated pancreatic tumorigenesis in vivo. We found that adiponectin significantly inhibited the apoptosis of both human and mouse pancreatic cancer cells via adipoR1, but not adipoR2. Furthermore, adiponectin can increase AMP-activated protein kinase (AMPK) phosphorylation and NAD-dependent deacetylase sirtuin-1 (Sirt1) of PC cells. Knockdown of AMPK or Sirt1 can increase the apoptosis in PC cells. AMPK up-regulated Sirt1, and Sirt1 can inversely phosphorylate AMPK. Further studies have shown that Sirt1 can deacetylate peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC1α), which can increase the expression levels of mitochondrial genes. Thus, adiponectin exerts potent anti-apoptotic effects on PC cells via the activation of AMPK/Sirt1/PGC1α signaling. Finally, adiponectin can elevate β-catenin levels. Taken together, these novel findings reveal an unconventional role of adiponectin in promoting pancreatic cancers, and suggest that the effects of adiponectin on tumorigenesis are highly tissue-dependent.

Indexed as

AdiponectinAMP-Activated Protein KinasesAnimalsApoptosisCaspase 3Cell Line, TumorCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticHEK293 CellsHep G2 CellsHumansImmunoblottingMice, Inbred C57BLMice, KnockoutAdiponectinadiponectin receptor 1, mouseAMP-Activated Protein KinasesCaspase 3Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mouseReceptors, AdiponectinSirt1 protein, mouseSirtuin 1Transcription Factors

Identifiers

PMID25051362
PMCPMC4148095
OpenAlexW1772625670

What OpenQuestion holds

Textmetadata
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.