Evidence map›Paper›PMID 27186436›Full record

ArticleAmerican journal of cancer research2016

Tumour-specific metabolic adaptation to acidosis is coupled to epigenetic stability in osteosarcoma cells.

Tokuhiro Chano, Sofia Avnet, Katsuyuki Kusuzaki, Gloria Bonuccelli, Pierre Sonveaux, Dante Rotili, Antonello Mai, Nicola Baldini

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Epigenetic Regulation Mediated by Sphingolipids in Cancer.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Osteosarcoma and Metastasis.Frontiers in oncology · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review
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

8 authors at 2 institutions in 2 countries.

Tokuhiro ChanoDepartment of Clinical Laboratory Medicine, Shiga University of Medical Science Otsu, Shiga, Japan.
Sofia AvnetOrthopaedic Pathophysiology and Regenerative Medicine Unit, Istituto Ortopedico Rizzoli Bologna, Italy.
Katsuyuki KusuzakiDepartment of Musculoskeletal Oncology, Takai Hospital Tennri, Nara, Japan.
Gloria BonuccelliOrthopaedic Pathophysiology and Regenerative Medicine Unit, Istituto Ortopedico Rizzoli Bologna, Italy.
Pierre SonveauxInstitut de Recherche Expérimentale et Clinique (IREC), Pole of Pharmacology (FATH), Université Catholique de Louvain (UCL) Brussels, Belgium.
Dante RotiliDepartment of Drug Chemistry and Technologies, Sapienza University of Roma Roma, Italy.
Antonello MaiDepartment of Drug Chemistry and Technologies, Sapienza University of RomaRoma, Italy; Pasteur Institute-Cenci Bolognetti Foundation, Sapienza University of RomaRoma, Italy.
Nicola BaldiniOrthopaedic Pathophysiology and Regenerative Medicine Unit, Istituto Ortopedico RizzoliBologna, Italy; Department of Biomedical and Neuromotor Sciences, University of BolognaBologna, Italy.
Sapienza University of Rome · ITShiga University of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The glycolytic-based metabolism of cancers promotes an acidic microenvironment that is responsible for increased aggressiveness. However, the effects of acidosis on tumour metabolism have been almost unexplored. By using capillary electrophoresis with time-of-flight mass spectrometry, we observed a significant metabolic difference associated with glycolysis repression (dihydroxyacetone phosphate), increase of amino acid catabolism (phosphocreatine and glutamate) and urea cycle enhancement (arginino succinic acid) in osteosarcoma (OS) cells compared with normal fibroblasts. Noteworthy, metabolites associated with chromatin modification, like UDP-glucose and N(8)-acetylspermidine, decreased more in OS cells than in fibroblasts. COBRA assay and acetyl-H3 immunoblotting indicated an epigenetic stability in OS cells than in normal cells, and OS cells were more sensitive to an HDAC inhibitor under acidosis than under neutral pH. Since our data suggest that acidosis promotes a metabolic reprogramming that can contribute to the epigenetic maintenance under acidosis only in tumour cells, the acidic microenvironment should be considered for future therapies.

Indexed as

Acidosisepigenomemetabolomeosteosarcoma

Identifiers

PMID27186436
PMCPMC4859889
OpenAlexW2403162493

What OpenQuestion holds

Textmetadata
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.