AXL-Driven Stemness and Hedgehog Signaling in HER2-Positive Breast Cancer with Acquired Trastuzumab Resistance: Synergistic Potential of AXL and HER2 Co-Targeting
Asiye Busra Boz, Idris Er, Enric Arasanz Picher, Sneha Smarakan

TL;DR
This study shows that AXL and hedgehog signaling contribute to trastuzumab resistance in HER2-positive breast cancer, and targeting both could improve treatment outcomes.
Contribution
The study reveals AXL's role in regulating stemness and hedgehog signaling, and proposes AXL and HER2 co-targeting as a novel strategy for overcoming resistance.
Findings
Trastuzumab resistance is linked to increased AXL expression and stemness.
AXL overexpression boosts hedgehog and stemness markers, while AXL silencing reduces them.
Combining AXL inhibition with trastuzumab reduces stemness and resistance.
Abstract
Stemness is a critical factor in tumor initiation, progression, metastasis, and resistance to treatment. The AXL receptor and hedgehog (Hh) signaling pathways play significant roles in regulating stemness, making them potential therapeutic targets. This study explores the involvement of AXL and hedgehog signaling in maintaining stemness and contributing to trastuzumab resistance in HER2-positive breast cancer. The expression of AXL and Hh markers was assessed in trastuzumab-resistant SKBR3 and HCC1954 cell lines and their parental counterparts. Trastuzumab resistance was associated with upregulation of AXL expression, with the GAS6/AXL axis identified as a regulator of stemness. Although inhibition of hedgehog signaling using GANT61 did not affect AXL expression, overexpression of AXL led to increased levels of hedgehog markers (e.g., Gli1, Ptch1) and stemness markers (e.g., Sox2, Oct4,…
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Taxonomy
TopicsPhagocytosis and Immune Regulation · Hedgehog Signaling Pathway Studies · Cancer Cells and Metastasis
