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Updated: Jun 29, 2025

Monitoring Hippo Signaling Pathway Activity Using a Luciferase-based Large Tumor Suppressor LATS Biosensor
Published on: September 13, 2018
Breast cancer drug resistance: Decoding the roles of Hippo pathway crosstalk
Fariba Dehghanian1, Laleh Ebrahimi Ghahnavieh1, Amirhossein Naghsh Nilchi1
1Department of Cell and Molecular Biology & Microbiology, Faculty of Biological Science and Technology, University of Isfahan, HezarJarib Street, Isfahan 81746-73441, Iran.
Abstract:
The most significant factors that lead to cancer-related death in breast cancer (BC) patients include drug resistance, migration, invasion, and metastasis. Several signaling pathways are involved in the development of BC. The different types of BC are initially sensitive to chemotherapy, and drug resistance can occur through multiple molecular mechanisms. Regardless of developing targeted Therapy, due to the heterogenic nature and complexity of drug resistance, it is a major clinical challenge with the low survival rate in BC patients. The deregulation of several signaling pathways, particularly the Hippo pathway (HP), is one of the most recent findings about the molecular mechanisms of drug resistance in BC, which are summarized in this review. Given that HP is one of the recent cancer research hotspots, this review focuses on its implication in BC drug resistance. Unraveling the different molecular basis of HP through its crosstalk with other signaling pathways, and determining the effectiveness of HP inhibitors can provide new insights into possible therapeutic strategies for overcoming chemoresistance in BC.
Insights
Drug resistance in breast cancer (BC) poses a major challenge. This review highlights the Hippo pathway's role in BC drug resistance and explores potential therapeutic strategies.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Breast cancer (BC) remains a leading cause of cancer-related death, significantly influenced by drug resistance, metastasis, and invasion.
- Chemotherapy resistance in BC is a complex clinical challenge, driven by diverse molecular mechanisms and the cancer's heterogeneous nature.
- Recent research implicates the deregulation of signaling pathways, notably the Hippo pathway (HP), in the development of BC drug resistance.
Purpose of the Study:
- This review summarizes the molecular mechanisms underlying Hippo pathway (HP) deregulation in breast cancer (BC) drug resistance.
- It focuses on the Hippo pathway as a recent area of cancer research and its specific implications in BC chemoresistance.
- The review aims to explore HP's crosstalk with other signaling pathways and evaluate the potential of HP inhibitors for overcoming resistance.
Main Methods:
- Literature review of recent studies on breast cancer signaling pathways and drug resistance.
- Analysis of molecular mechanisms involving the Hippo pathway (HP) in BC.
- Examination of the crosstalk between HP and other signaling pathways relevant to chemoresistance.
Main Results:
- Deregulation of the Hippo pathway (HP) is identified as a key molecular mechanism contributing to drug resistance in breast cancer (BC).
- The review details the complex interplay and crosstalk between HP and other signaling pathways involved in BC progression and resistance.
- Understanding these molecular underpinnings is crucial for developing effective therapeutic strategies.
Conclusions:
- The Hippo pathway (HP) plays a significant role in the molecular basis of drug resistance in breast cancer (BC).
- Further investigation into HP's function and its interactions with other pathways is essential for advancing BC treatment.
- Targeting the Hippo pathway holds promise for developing novel therapeutic strategies to overcome chemoresistance in BC patients.
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