Interactions between ADGRF1 (GPR110) and extracellular matrix proteins govern its effects on tumorigenesis in HER2‐positive breast cancer

ADGRF1 switches from a tumour-promoting to tumour-suppressive function upon interaction with laminin-111, leading to improvements in sensitivity to anti-HER2 drugs. Leveraging ADGRF1 interactions with laminin-111 may allow the design of novel therapies against ADGRF1 in HER2+ BC.

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Publication Details

Journal
British Journal of Pharmacology
Published
2025-02-18
DOI
https://doi.org/10.1111/bph.17463
Citations
6
Primary Topic
HER2/EGFR in Cancer Research
Type
article
Field-Weighted Citation Impact
6.27

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article

Interactions between ADGRF1 (GPR110) and extracellular matrix proteins govern its effects on tumorigenesis in HER2‐positive breast cancer

Martin J. Shea, Raksha R. Bhat, Suhas Vasaikar, Micah Castillo et al.
6 citations
British Journal of Pharmacology
HER2/EGFR in Cancer Research
6.27
article

Interactions between ADGRF1 (GPR110) and extracellular matrix proteins govern its effects on tumorigenesis in HER2‐positive breast cancer

Martin J. Shea, Raksha R. Bhat, Suhas Vasaikar, Micah Castillo, Rachel Schiff, Meghana V. Trivedi, Preethi H. Gunaratne, Tahir Hussain, Tasneem Bawa‐Khalfe, Jamunarani Veeraraghavan, Sarmistha Nanda, Hee‐Yong Kim, Alexis Ruiz, Sung Yun Jung, Wangjia Cao, Noor Mazin Abdulkareem, Xinli Liu
article en
6 citations

Abstract

ADGRF1 switches from a tumour-promoting to tumour-suppressive function upon interaction with laminin-111, leading to improvements in sensitivity to anti-HER2 drugs. Leveraging ADGRF1 interactions with laminin-111 may allow the design of novel therapies against ADGRF1 in HER2+ BC.

British Journal of PharmacologyVol. 182(11)
Baylor College of Medicine (US), National Institute on Alcohol Abuse and Alcoholism (US), University of Houston (US), Seagen (United States) (US)
U.S. Department of Defense, Breast Cancer Research Foundation, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 4%
HER2/EGFR in Cancer Research
6.27
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