Evidence map›Paper›PMID 41715254›Full record

ArticleBiological research2026

The polyamine inhibitor SAM486A increases the efficacy of adagrasib in non-small cell lung cancer cells harboring KRAS

Antonia Martin-Martin, Carina Chipón, Constanza Guzman-Kunstmann, Sergio Guzman-Kunstmann, Neudo Buelvas, Claudio Henríquez, Francisca Vidal, Franz Villarroel-Espindola, Trista K Hinz, Lynn E Heasley and 1 more

Abstract read
In one paragraph

Article in Biological research, 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

11 authors.

Antonia Martin-MartinInstituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, PO. 5090000, Valdivia, Chile.
Carina ChipónInstituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, PO. 5090000, Valdivia, Chile.
Constanza Guzman-KunstmannInstituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, PO. 5090000, Valdivia, Chile.
Sergio Guzman-KunstmannInstituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, PO. 5090000, Valdivia, Chile.
Neudo BuelvasInstituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, PO. 5090000, Valdivia, Chile.
Claudio HenríquezInstituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, PO. 5090000, Valdivia, Chile.
Francisca VidalUnidad Medicina Traslacional, Instituto Oncológico Fundación Arturo López Pérez, Santiago, Chile.
Franz Villarroel-EspindolaUnidad Medicina Traslacional, Instituto Oncológico Fundación Arturo López Pérez, Santiago, Chile.
Trista K HinzSchool of Dental Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.
Lynn E HeasleySchool of Dental Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.
Rodrigo A López-MuñozInstituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, PO. 5090000, Valdivia, Chile. rodrigo.lopez@uach.cl.ORCID http://orcid.org/0000-0003-1825-8563

Funding

Agencia Nacional de Investigación y Desarrollo FONDAP 1523A0008 (ACCDiS)Agencia Nacional de Investigación y Desarrollo FONDECYT 1221415Agencia Nacional de Investigación y Desarrollo FONDECYT 1241400BLRD VA I01 BX004751U.S. Department of Veterans Affairs VA Merit Grant BX004751-05
6 · The paper itself

Abstract

backgroundNon-small cell lung cancer (NSCLC) accounts for most lung cancer cases and poses major challenges due to late-stage diagnosis and limited options. A substantial subset of NSCLC harbors KRAS mutations, most commonly at codon 12. Although KRAS

methodsIn vitro assays included viability (MTT), clonogenic, BrdU incorporation, and Western blot analyses across four NSCLC cell lines. Drug-drug interactions were quantified using Combenefit software. In vivo efficacy was tested in C57BL/6 mice using an orthotopic model with LLC46 (KRAS

resultsIn vitro, adagrasib reduced AMD1 levels, and SAM486A synergistically enhanced its antiproliferative effects, particularly in KRAS

conclusionsOur results suggest that targeting polyamine metabolism with SAM486A enhances the efficacy of KRAS

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsPolyaminesProto-Oncogene Proteins p21(ras)AnimalsCell Line, TumorCell ProliferationHumansMiceMice, Inbred C57BLMutationKRAS protein, humanPolyaminesProto-Oncogene Proteins p21(ras)Drug combinationsKRAS inhibitorsNon-small cell lung cancerPolyamines

Identifiers

PMID41715254
PMCPMC13020075

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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.