Evidence map›Paper›PMID 32138158›Full record

ReviewCells2020

Multifaceted Aspects of Metabolic Plasticity in Human Cholangiocarcinoma: An Overview of Current Perspectives.

Mirella Pastore, Giulia Lori, Alessandra Gentilini, Maria Letizia Taddei, Giovanni Di Maira, Claudia Campani, Stefania Recalcati, Pietro Invernizzi, Fabio Marra, Chiara Raggi

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Identification of the function ofTranslational cancer research · 2023
    Article
  8. Review
  9. Review
  10. 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

10 authors at 3 institutions in 1 country.

Mirella PastoreDepartment of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Giulia LoriDepartment of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Alessandra GentiliniDepartment of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Maria Letizia TaddeiDepartment of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Giovanni Di MairaDepartment of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Claudia CampaniDepartment of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Stefania RecalcatiDepartment of Biomedical Sciences for Health, University of Milan, 20133 Milan, Italy.
Pietro InvernizziDivision of Gastroenterology and Center for Autoimmune Liver Diseases, San Gerardo Hospital, Department of Medicine and Surgery, University of Milan-Bicocca, 20900 Monza, Italy.
Fabio MarraDepartment of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Chiara RaggiDepartment of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
University of Florence · ITUniversity of Milan · ITUniversity of Milano-Bicocca · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholangiocarcinoma (CCA) is a deadly tumor without an effective therapy. Unique metabolic and bioenergetics features are important hallmarks of tumor cells. Metabolic plasticity allows cancer cells to survive in poor nutrient environments and maximize cell growth by sustaining survival, proliferation, and metastasis. In recent years, an increasing number of studies have shown that specific signaling networks contribute to malignant tumor onset by reprogramming metabolic traits. Several evidences demonstrate that numerous metabolic mediators represent key-players of CCA progression by regulating many signaling pathways. Besides the well-known Warburg effect, several other different pathways involving carbohydrates, proteins, lipids, and nucleic acids metabolism are altered in CCA. The goal of this review is to highlight the main metabolic processes involved in the cholangio-carcinogeneis that might be considered as potential novel druggable candidates for this disease.

Indexed as

Bile Duct NeoplasmsCell PlasticityCell ProliferationCholangiocarcinomaHumansMitochondriacholangiocarcinomafatty acidsfatty acid synthasemitochondriaOXPHOSPGC-1αtricarboxylic acid cycle

Identifiers

PMID32138158
PMCPMC7140515
OpenAlexW3010150434

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.