Evidence map›Paper›PMID 40332401›Full record

ArticleInternational journal of molecular sciences2025

Lapatinib-Resistant HER2+ Breast Cancer Cells Are Associated with Dysregulation of MAPK and p70S6K/PDCD4 Pathways and Calcium Management, Influence of Cryptotanshinone.

Jorge Hernández-Valencia, Ruth García-Villarreal, Manuel Rodríguez-Jiménez, Alex Daniel Hernández-Avalos, Ignacio A Rivero, José Luis Vique-Sánchez, Brenda Chimal-Vega, Angel Pulido-Capiz, Victor García-González

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

9 authors.

Jorge Hernández-ValenciaDepartamento de Bioquímica, Facultad de Medicina Mexicali, Universidad Autónoma de Baja California, Mexicali 21100, Baja California, Mexico.ORCID 0000-0002-4548-6812
Ruth García-VillarrealDepartamento de Bioquímica, Facultad de Medicina Mexicali, Universidad Autónoma de Baja California, Mexicali 21100, Baja California, Mexico.ORCID 0009-0001-0268-3437
Manuel Rodríguez-JiménezDepartamento de Bioquímica, Facultad de Medicina Mexicali, Universidad Autónoma de Baja California, Mexicali 21100, Baja California, Mexico.
Alex Daniel Hernández-AvalosDepartamento de Bioquímica, Facultad de Medicina Mexicali, Universidad Autónoma de Baja California, Mexicali 21100, Baja California, Mexico.ORCID 0009-0003-0856-146X
Ignacio A RiveroCentro de Graduados e Investigación en Química, Tecnológico Nacional de México, Instituto Tecnológico de Tijuana, Tijuana 22510, Baja California, Mexico.ORCID 0000-0003-4920-6379
José Luis Vique-SánchezCentro de Ciencias de la Salud Mexicali, Universidad Autónoma de Baja California, Mexicali 21000, Baja California, Mexico.
Brenda Chimal-VegaDepartamento de Bioquímica, Facultad de Medicina Mexicali, Universidad Autónoma de Baja California, Mexicali 21100, Baja California, Mexico.ORCID 0000-0002-2238-0708
Angel Pulido-CapizDepartamento de Bioquímica, Facultad de Medicina Mexicali, Universidad Autónoma de Baja California, Mexicali 21100, Baja California, Mexico.ORCID 0000-0001-9650-2555
Victor García-GonzálezDepartamento de Bioquímica, Facultad de Medicina Mexicali, Universidad Autónoma de Baja California, Mexicali 21100, Baja California, Mexico.ORCID 0000-0002-9421-3730

Funding

Coordinación General de Investigación y Posgrado/UABC 23a. Convocatoria Interna de Apoyo a Proyectos de Investigación (2-12-213-2-003-2-1994)Fondo Sectorial de Investigación para la Educación CB 2017-2018 A1-S-28653/SEP/CONACYTPrograma Presupuestario F003 Programas Nacionales Estratégicos de Ciencia, Tecnología y Vinculación con los Sectores Social, Público y Privado
6 · The paper itself

Abstract

Resistance to HER2 tyrosine-kinase inhibitor Lapatinib (Lap) is one of the leading causes of cancer treatment failure in HER2+ breast cancer (BC), associated with an aggressive tumor phenotype. Cryptotanshinone (Cry) is a natural terpene molecule that could function as a chemosensitizer by disturbing estrogen receptor (ERα) signaling and inhibiting the protein translation factor-4A, eIF4A. Therefore, we evaluated Cry dual regulation on eIF4A and ERα. This study aimed to elucidate the underlying mechanisms of Lap chemoresistance and the impact of Cry on them. We generated two Lap-resistant BT474 cell HER2+ variants named BT474

Indexed as

Apoptosis Regulatory ProteinsBreast NeoplasmsCalciumDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesLapatinibPhenanthrenesRibosomal Protein S6 Kinases, 70-kDaRNA-Binding ProteinsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMAP Kinase Signaling SystemSignal TransductionApoptosis Regulatory ProteinsCalciumcryptotanshinoneERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesLapatinibPhenanthrenesRibosomal Protein S6 Kinases, 70-kDaRNA-Binding Proteinsbreast cancer HER2+calcium homeostasischemoresistancecryptotanshinonelapatinib

Identifiers

PMID40332401
PMCPMC12027730

What OpenQuestion holds

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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.