Evidence map›Paper›PMID 40748136›Full record

ArticleEndocrine-related cancer2025

Targeting Src tyrosine kinase to enhance radioiodide uptake in breast cancer.

Vikki L Poole, Mohammed M Alshahrani, Selvambigai Manivannan, Iñigo Landa, Aditi Hariharan, Rebecca J Thompson, Merve Kocbiyik, Caitlin E M Thornton, Katie Brookes, Alice Fletcher and 4 more

Abstract read
In one paragraph

Article in Endocrine-related cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Vikki L PooleDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.
Mohammed M AlshahraniDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.
Selvambigai ManivannanDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.
Iñigo LandaInstitut Gustave Roussy, Inserm U981, Villejuif, France.ORCID 0000-0002-2817-8295
Aditi HariharanDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.
Rebecca J ThompsonDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.
Merve KocbiyikDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.
Caitlin E M ThorntonDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.
Katie BrookesDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.
Alice FletcherDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.
Kristien BoelaertDepartment of Applied Health Sciences, College of Medicine and Health, University of Birmingham, Birmingham, UK.
Martin L ReadDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.ORCID 0000-0001-8918-4333
Christopher J McCabeDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.ORCID 0000-0002-8687-3405
Vicki E SmithDepartment of Metabolism & Systems Science (MSS) and Centre for Endocrinology, Diabetes and Metabolism (CEDAM), College of Medicine and Health, University of Birmingham, Birmingham, UK.ORCID 0000-0003-0757-7198

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sodium iodide symporter (NIS) expression in breast cancer renders radioiodide (RAI) a promising treatment modality. However, insufficient functional NIS within the plasma membrane limits RAI uptake (RAIU). We aimed to elucidate NIS regulatory mechanisms that impede RAIU in breast cancer and identify molecular targets for stimulating RAI-avidity in breast tumours. Mechanistic interaction between pituitary tumor-transforming gene-binding factor (PBF/PTTG1IP) and NIS was investigated through NanoBiT, co-immunoprecipitation, immunofluorescent microscopy, subcellular localisation and RAIU assays utilising wild-type and CRISPR-Cas9 PBF knockout breast cancer cells. In breast cancer cells, NIS:PBF interaction resulted in diminished RAIU, reversible through reduced PBF phosphorylation by the Src inhibitor dasatinib. Src overexpression diminished RAIU in a PBF-dependent manner that was mediated by Src myristoylation by N-myristoyltransferase 1 (NMT1). NMT1 inhibition significantly enhanced RAIU via Src and PBF in breast and thyroid cancer cells. Bioinformatic analyses revealed clinical associations between high Src and NMT1 expression and increased tumour recurrence in RAI-treated thyroid cancers indicating RAI-resistance. In breast cancer, high PBF and Src expression was associated with the more aggressive tumours that are most likely to benefit from targeted RAI therapy. We describe a new NIS regulatory pathway in breast cancer cells via Src myristoylation and PBF phosphorylation and show that the same pathway exists in thyroid cells, the canonical setting for the exploitation of NIS function. These findings reveal that PBF interaction with NIS may be modulated by Src, which in turn is susceptible to NMT inhibition, and suggest that targeting NMT1 may represent an innovative approach for augmenting RAI-avidity in breast cancer.

Indexed as

Breast NeoplasmsIodine Radioisotopessrc-Family KinasesCell Line, TumorDasatinibFemaleHumansSecurinSodium-Iodide SymportersSymportersDasatinibIodine Radioisotopespituitary tumor-transforming protein 1, humanSecurinSodium-Iodide Symporterssrc-Family KinasesSymportersbreast cancerNISPBF/PTTG1IPradioiodideSrc myristoylation

Identifiers

PMID40748136
PMCPMC12372067

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.