Evidence map›Paper›PMID 42435178›Full record

ReviewAdvances in experimental medicine and biology2026

Targeting Lung Cancer Metabolism: Therapeutic Opportunities and Challenges.

Catarina Freitas-Dias, Cindy Mendes

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.

Catarina Freitas-DiasiNOVA4Health, NOVA Medical School | Faculdade de Ciências Médicas, NMS, FCM, Universidade NOVA de Lisboa, Lisboa, Portugal.
Cindy MendesiNOVA4Health, NOVA Medical School | Faculdade de Ciências Médicas, NMS, FCM, Universidade NOVA de Lisboa, Lisboa, Portugal. cindy.mendes@nms.unl.pt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer remains the leading cause of cancer-related deaths worldwide in both men and women. Although conventional chemotherapy has been the backbone of treatment, it often fails to provide long-term survival benefits for most patients. In recent years, advances in the understanding of molecular and genetic alterations in lung cancer have led to the identification of distinct subtypes and the development of targeted therapies. However, these therapies benefit only a limited group of patients with specific driver mutations. Similarly, immunotherapy has brought new hope, yet access and efficacy remain variable across the patient population. As the field evolves, there is growing recognition that cancer metabolism plays a crucial role in tumor progression, immune evasion, and resistance to therapy. This chapter will examine the metabolic reprogramming that occurs in lung cancer cells, including alterations in glycolysis, glutaminolysis, and lipid metabolism, within the context of the tumor microenvironment. It will also examine how these changes impact current treatments and highlight emerging therapeutic strategies targeting cancer metabolism.

Indexed as

Antineoplastic AgentsLung NeoplasmsMolecular Targeted TherapyAnimalsGlycolysisHumansImmunotherapyLipid MetabolismMetabolic ReprogrammingTumor MicroenvironmentAntineoplastic AgentsLung cancerMetabolic adaptationMetabolic remodelingMetabolism-directed therapiesTherapy responseTumor microenvironment

Identifiers

What Socratic 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 Socratic graph.