Evidence map›Paper›PMID 38885414›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

A Novel AMPK Inhibitor Sensitizes Pancreatic Cancer Cells to Ferroptosis Induction.

Carolin Schneider, Jorina Hilbert, Franziska Genevaux, Stefanie Höfer, Lukas Krauß, Felix Schicktanz, Constanza Tapia Contreras, Shaishavi Jansari, Aristeidis Papargyriou, Thorsten Richter and 23 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Reprogramming of fatty acid metabolism in thyroid cancer: Potential targets and mechanisms.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2025
    Article
  9. Review
  10. Article
  11. Review
  12. A Novel AMPK Inhibitor Sensitizes Pancreatic Cancer Cells to Ferroptosis Induction.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    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

33 authors.

Carolin SchneiderDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Jorina HilbertDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Franziska GenevauxMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, 81675, Munich, Germany.
Stefanie HöferProteomics and Bioanalytics, Department of Molecular Life Sciences, School of Life Sciences, Technical University of Munich, 85354, Freising, Germany.
Lukas KraußDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Felix SchicktanzInstitute of Pathology, Technical University of Munich, 81675, Munich, Germany.
Constanza Tapia ContrerasDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Shaishavi JansariDepartment of Gynecology and Obstetrics, University Medical Center Göttingen, Göttingen, Germany.
Aristeidis PapargyriouMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, 81675, Munich, Germany.
Thorsten RichterDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Abdallah M AlfayomyDepartment of Medicinal Chemistry, Institute of Pharmacy, Martin-Luther University Halle-Wittenberg, 06120, Halle (Saale), Germany.
Chiara FalcomatàInstitute for Translational Cancer Research and Experimental Cancer Therapy, Technical University Munich, 81675, Munich, Germany.
Christian SchneeweisInstitute for Translational Cancer Research and Experimental Cancer Therapy, Technical University Munich, 81675, Munich, Germany.
Felix OrbenMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, 81675, Munich, Germany.
Ruppert ÖllingerInstitute of Molecular Oncology and Functional Genomics, TUM School of Medicine, Technical University of Munich, 81675, Munich, Germany.
Florian WegwitzDepartment of Gynecology and Obstetrics, University Medical Center Göttingen, Göttingen, Germany.
Angela BoshnakovskaDepartment of Cellular Biochemistry, University Medical Center, 37073, Göttingen, Germany.
Peter RehlingDepartment of Cellular Biochemistry, University Medical Center, 37073, Göttingen, Germany.
Denise MüllerInstitute of Pathology, University Medical Center, 37075, Göttingen, Germany.
Philipp StröbelInstitute of Pathology, University Medical Center, 37075, Göttingen, Germany.
Volker EllenriederClinical Research Unit 5002, KFO5002, University Medical Center Göttingen, 37075, Göttingen, Germany.
Lena ConradiDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Elisabeth HessmannClinical Research Unit 5002, KFO5002, University Medical Center Göttingen, 37075, Göttingen, Germany.
Michael GhadimiDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Marian GradeDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Matthias WirthDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.
Katja SteigerInstitute of Pathology, Technical University of Munich, 81675, Munich, Germany.
Roland RadInstitute of Molecular Oncology and Functional Genomics, TUM School of Medicine, Technical University of Munich, 81675, Munich, Germany.
Bernhard KusterProteomics and Bioanalytics, Department of Molecular Life Sciences, School of Life Sciences, Technical University of Munich, 85354, Freising, Germany.
Wolfgang SipplDepartment of Medicinal Chemistry, Institute of Pharmacy, Martin-Luther University Halle-Wittenberg, 06120, Halle (Saale), Germany.
Maximilian ReichertMedical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich, 81675, Munich, Germany.
Dieter SaurInstitute for Translational Cancer Research and Experimental Cancer Therapy, Technical University Munich, 81675, Munich, Germany.
Günter SchneiderDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075, Göttingen, Germany.ORCID 0000-0003-1840-4508

Funding

Bavarian Ministry of Economic Affairs 01KD2206PBavarian Ministry of Economic Affairs 01KD2208BBavarian Ministry of Economic Affairs 13N16450Bavarian Ministry of Economic Affairs BMBFBavarian Ministry of Economic Affairs LSM-2104-0017Deutsche Forschungsgemeinschaft ID329628492(SFB1321)Deutsche Forschungsgemeinschaft KFO5002Deutsche Forschungsgemeinschaft RE 3723/4-1Deutsche Forschungsgemeinschaft RE 3723/6-1Deutsche Forschungsgemeinschaft SCHN 959/3-2Deutsche Forschungsgemeinschaft SCHN 959/6-1Deutsche Forschungsgemeinschaft SCHN959/7-1Deutsche Forschungsgemeinschaft SCHN959/8-1Deutsche Forschungsgemeinschaft WI 6148/1-1DKTK (German Cancer Consortium) Strategic Initiative Organoid PlatformGerman Cancer Aid 111273German Cancer Aid 70113760German Cancer Aid 70115444Wilhelm-Sander-Stiftung 2022.074.1Wilhelm-Sander-Stiftung 2023.027.1
6 · The paper itself

Abstract

Cancer cells must develop strategies to adapt to the dynamically changing stresses caused by intrinsic or extrinsic processes, or therapeutic agents. Metabolic adaptability is crucial to mitigate such challenges. Considering metabolism as a central node of adaptability, it is focused on an energy sensor, the AMP-activated protein kinase (AMPK). In a subtype of pancreatic ductal adenocarcinoma (PDAC) elevated AMPK expression and phosphorylation is identified. Using drug repurposing that combined screening experiments and chemoproteomic affinity profiling, it is identified and characterized PF-3758309, initially developed as an inhibitor of PAK4, as an AMPK inhibitor. PF-3758309 shows activity in pre-clinical PDAC models, including primary patient-derived organoids. Genetic loss-of-function experiments showed that AMPK limits the induction of ferroptosis, and consequently, PF-3758309 treatment restores the sensitivity toward ferroptosis inducers. The work established a chemical scaffold for the development of specific AMPK-targeting compounds and deciphered the framework for the development of AMPK inhibitor-based combination therapies tailored for PDAC.

Indexed as

AMP-Activated Protein KinasesFerroptosisPancreatic NeoplasmsAnimalsCarcinoma, Pancreatic DuctalCell Line, TumorHumansMiceAMP-Activated Protein KinasesAMPKferroptosispancreatic cancer

Identifiers

PMID38885414
PMCPMC11336956

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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.