Evidence map›Paper›PMID 25805929›Full record

ReviewWorld journal of gastroenterology2015

Mitochondrial uncoupling protein 2 and pancreatic cancer: a new potential target therapy.

Massimo Donadelli, Ilaria Dando, Elisa Dalla Pozza, Marta Palmieri

Registry-linked trialOpen access · hybridAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05587088 (Evaluation of the Safety and Efficacy of Esperanza Extract), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 9% 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.

NCT05587088 phase1 / phase2unknown statusnot on this mapstarted 2022, after this paper: background citation

Evaluation of the Safety and Efficacy of Esperanza Extract (Petiveria Alliacea) in Patients With Metastatic Gastrointestinal Tumors and Acute Leukemia

TypeinterventionalSponsorHospital Universitario San IgnacioRan2022 to 2023Enrolled82ConditionsNeoplasm, Stomach, Gastric Neoplasms Malignant, Pancreatic Neoplasms, Colorectal NeoplasmsArmsPetiveria Alliacea Preparation, Placebo
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Proteomics in pancreatic cancer.Biomarker research · 2025
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. UCP2 - Taking the heat out of P-glycoprotein?Cancer drug resistance (Alhambra, Calif.) · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. The enhancement of glycolysis regulates pancreatic cancer metastasis.Cellular and molecular life sciences : CMLS · 2020
    Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Massimo DonadelliMassimo Donadelli, Ilaria Dando, Elisa Dalla Pozza, Marta Palmieri, Department of Life and Reproduction Sciences, Biochemistry Section, University of Verona, 37134 Verona, Italy.
Ilaria DandoMassimo Donadelli, Ilaria Dando, Elisa Dalla Pozza, Marta Palmieri, Department of Life and Reproduction Sciences, Biochemistry Section, University of Verona, 37134 Verona, Italy.
Elisa Dalla PozzaMassimo Donadelli, Ilaria Dando, Elisa Dalla Pozza, Marta Palmieri, Department of Life and Reproduction Sciences, Biochemistry Section, University of Verona, 37134 Verona, Italy.
Marta PalmieriMassimo Donadelli, Ilaria Dando, Elisa Dalla Pozza, Marta Palmieri, Department of Life and Reproduction Sciences, Biochemistry Section, University of Verona, 37134 Verona, Italy.
University of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overall 5-years survival of pancreatic cancer patients is nearly 5%, making this cancer type one of the most lethal neoplasia. Furthermore, the incidence rate of pancreatic cancer has a growing trend that determines a constant increase in the number of deceases caused by this pathology. The poor prognosis of pancreatic cancer is mainly caused by delayed diagnosis, early metastasis of tumor, and resistance to almost all tested cytotoxic drugs. In this respect, the identification of novel potential targets for new and efficient therapies should be strongly encouraged in order to improve the clinical management of pancreatic cancer. Some studies have shown that the mitochondrial uncoupling protein 2 (UCP2) is over-expressed in pancreatic cancer as compared to adjacent normal tissues. In addition, recent discoveries established a key role of UCP2 in protecting cancer cells from an excessive production of mitochondrial superoxide ions and in the promotion of cancer cell metabolic reprogramming, including aerobic glycolysis stimulation, promotion of cancer progression. These observations together with the demonstration that UCP2 repression can synergize with standard chemotherapy to inhibit pancreatic cancer cell growth provide the molecular rationale to consider UCP2 as a potential therapeutic target for pancreatic cancer. In this editorial, recent advances describing the relationship between cancer development and mitochondrial UCP2 activity are critically provided.

Indexed as

Signal TransductionAnimalsAntineoplastic AgentsBiomarkers, TumorHumansIon ChannelsMitochondrial ProteinsMolecular Targeted TherapyPancreatic NeoplasmsUncoupling Protein 2Up-RegulationAntineoplastic AgentsBiomarkers, TumorIon ChannelsMitochondrial ProteinsUCP2 protein, humanUncoupling Protein 2MetabolismPancreatic cancerReactive oxygen speciesTarget therapyUncoupling protein 2

Identifiers

PMID25805929
PMCPMC4363752
OpenAlexW2183106106

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.