Evidence map›Paper›PMID 35666002›Full record

ReviewMolecular oncology2022

Metabolic reprogramming: a bridge between aging and tumorigenesis.

Stanislav Drapela, Didem Ilter, Ana P Gomes

Open access · goldAbstract readReview
In one paragraph

Review in Molecular oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.6field-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.

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

30 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Imaging Cellular Metabolic Rewiring with SuMMIT-SRS.bioRxiv : the preprint server for biology · 2025
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Host-directed therapy for tuberculosis.European journal of medical research · 2025
    Review
  16. Review
  17. Article
  18. Review
  19. American journal of translational research · 2025
    Article
  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

3 authors at 1 institution in 1 country.

Stanislav DrapelaDepartment of Molecular Oncology, H. Lee Moffit Cancer Center & Research Institute, Tampa, FL, USA.ORCID 0000-0002-9421-9972
Didem IlterDepartment of Molecular Oncology, H. Lee Moffit Cancer Center & Research Institute, Tampa, FL, USA.
Ana P GomesDepartment of Molecular Oncology, H. Lee Moffit Cancer Center & Research Institute, Tampa, FL, USA.ORCID 0000-0003-0881-727X
Moffitt Cancer Center · US

Funding

Vitamin B12 supplementation as novel therapeutic strategy to improve cancer-associated outcomesR00CA218686 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI DA SILVA GOMES, ANA · 2020 to 2022
$916k
NCI NIH HHS R00 CA218686
6 · The paper itself

Abstract

Aging is the most robust risk factor for cancer development, with more than 60% of cancers occurring in those aged 60 and above. However, how aging and tumorigenesis are intertwined is poorly understood and a matter of significant debate. Metabolic changes are hallmarks of both aging and tumorigenesis. The deleterious consequences of aging include dysfunctional cellular processes, the build-up of metabolic byproducts and waste molecules in circulation and within tissues, and stiffer connective tissues that impede blood flow and oxygenation. Collectively, these age-driven changes lead to metabolic reprogramming in different cell types of a given tissue that significantly affects their cellular functions. Here, we put forward the idea that metabolic changes that happen during aging help create a favorable environment for tumorigenesis. We review parallels in metabolic changes that happen during aging and how these changes function both as adaptive mechanisms that enable the development of malignant phenotypes in a cell-autonomous manner and as mechanisms that suppress immune surveillance, collectively creating the perfect environment for cancers to thrive. Hence, antiaging therapeutic strategies that target the metabolic reprogramming that occurs as we age might provide new opportunities to prevent cancer initiation and/or improve responses to standard-of-care anticancer therapies.

Indexed as

Cell Transformation, NeoplasticNeoplasmsHumansagingcellular energeticsimmune responsemetabolic reprogrammingtumorigenesis

Identifiers

PMID35666002
PMCPMC9490145
OpenAlexW4281620894

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.