Evidence map›Paper›PMID 33401522›Full record

ReviewCancers2021

MicroRNA-Mediated Metabolic Shaping of the Tumor Microenvironment.

Federico Virga, Lorena Quirico, Stefania Cucinelli, Massimiliano Mazzone, Daniela Taverna, Francesca Orso

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

17 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Acid affairs in anti-tumour immunity.Cancer cell international · 2024
    Review
  9. MicroRNAs in metabolism for precision treatment of lung cancer.Cellular & molecular biology letters · 2024
    Review
  10. Stroma-derived miR-214 coordinates tumor dissemination.Journal of experimental & clinical cancer research : CR · 2023
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. 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

6 authors at 2 institutions in 2 countries.

Federico VirgaMolecular Biotechnology Center (MBC), University of Torino, 10126 Torino, Italy.
Lorena QuiricoMolecular Biotechnology Center (MBC), University of Torino, 10126 Torino, Italy.
Stefania CucinelliMolecular Biotechnology Center (MBC), University of Torino, 10126 Torino, Italy.
Massimiliano MazzoneMolecular Biotechnology Center (MBC), University of Torino, 10126 Torino, Italy.
Daniela TavernaMolecular Biotechnology Center (MBC), University of Torino, 10126 Torino, Italy.
Francesca OrsoMolecular Biotechnology Center (MBC), University of Torino, 10126 Torino, Italy.ORCID 0000-0003-4706-6464
University of Turin · ITVIB-KU Leuven Center for Cancer Biology · BE

Funding

Associazione Italiana per la Ricerca sul Cancro 24188LQAssociazione Italiana per la Ricerca sul Cancro IG2013-14201DTAssociazione Italiana per la Ricerca sul Cancro IG2017-20258DTEuropean Research Council 773208Fondazione CRT 2018.1311DTRegione Piemonte DEFLECT- 320-44
6 · The paper itself

Abstract

The metabolism of cancer cells is generally very different from what is found in normal counterparts. However, in a tumor mass, the continuous crosstalk and competition for nutrients and oxygen among different cells lead to metabolic alterations, not only in cancer cells, but also in the different stromal and immune cells of the tumor microenvironment (TME), which are highly relevant for tumor progression. MicroRNAs (miRs) are small non-coding RNAs that silence their mRNA targets post-transcriptionally and are involved in numerous physiological cell functions as well as in the adaptation to stress situations. Importantly, miRs can also be released via extracellular vesicles (EVs) and, consequently, take part in the bidirectional communication between tumor and surrounding cells under stress conditions. Certain miRs are abundantly expressed in stromal and immune cells where they can regulate various metabolic pathways by directly suppressing enzymes or transporters as well as by controlling important regulators (such as transcription factors) of metabolic processes. In this review, we discuss how miRs can induce metabolic reprogramming in stromal (fibroblasts and adipocytes) and immune (macrophages and T cells) cells and, in turn, how the biology of the different cells present in the TME is able to change. Finally, we debate the rebound of miR-dependent metabolic alterations on tumor progression and their implications for cancer management.

Indexed as

metabolismmiRtumor microenvironment

Identifiers

PMID33401522
PMCPMC7795884
OpenAlexW3118547187

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.