Evidence map›Paper›PMID 42435165›Full record

ReviewAdvances in experimental medicine and biology2026

The Interdependence of Carbon Substrates and Metabolic Pathways Enables the Metabolic Plasticity of Cancer Cells.

Inês Serpa-Gonçalves, Jacinta Serpa

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Inês Serpa-GonçalvesiNOVA4Health, NOVA Medical School | Faculdade de Ciências Médicas, NMS, FCM, Universidade NOVA de Lisboa, Lisboa, Portugal.
Jacinta SerpaiNOVA4Health, NOVA Medical School | Faculdade de Ciências Médicas, NMS, FCM, Universidade NOVA de Lisboa, Lisboa, Portugal. jacinta.serpa@nms.unl.pt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor microenvironment (TME) functions as a dynamic and co-evolving ecosystem, where malignant and non-malignant cells form a metabolically interdependent community. This ecological view reimagines tumors not as isolated cell masses, but as complex biotopes in which cellular interactions are integral to tumor initiation, growth, and progression. A hallmark of this adaptive environment is metabolic plasticity-an essential mechanism that enables tumor cells, including the metastatic ones, to reprogram their metabolism in response to fluctuating nutrient availability and environmental stressors. At the core of this reprogramming lies carbon metabolism, characterized by the selective and flexible utilization of key metabolites, including glucose, lactate, glutamine, cysteine, and fatty acids. These compounds support energy production, biomass synthesis, and redox balance, while also facilitating the export and repurposing of metabolic byproducts for signaling or reuse. This chapter presents a conceptual framework that explores the interdependence of central metabolic pathways, emphasizing how tumors coordinate energy generation, biosynthesis, and redox control to support malignant progression.

Indexed as

CarbonEnergy MetabolismMetabolic Networks and PathwaysNeoplasmsTumor MicroenvironmentAnimalsGlucoseGlutamineGlycolysisHumansMetabolic ReprogrammingOxidation-ReductionCarbonGlucoseGlutamineGluconeogenesisGlutaminolysisGlycolysisInterconnected metabolic pathwaysMetabolic dependenceMetabolism-targeted therapiesPentose phosphate pathway (PPP)

Identifiers

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.