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Updated: Apr 7, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Implications of Akt2/Twist crosstalk on breast cancer metastatic outcome
Lucília Pereira1, Sara Horta2, Rita Mateus2
1Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica, Portugal.
Abstract:
Akt2 is a pivotal player in a complex web of signaling pathways controlling cell growth, proliferation, and survival. The deregulation or aberrations of Akt2 have been associated with tumor progression, metastatic spread, and, lastly, chemoresistance. The impairment of its activity has gained more attention because Akt2 is intertwined with a range of signaling paths, including the Phosphatidylinositol 3 kinase/Akt/Mammalian target of rapamycin (PI3K/mTOR) signaling axis, which are involved in macromolecules synthesis and metabolism. Here, we focus on Akt2 because of its involvement in the acquisition of stem cell-like properties, responsible for invasiveness and chemoresistance, also promoted by Twist. We also suggest therapeutic strategies targeting Akt2 to overcome the drawbacks of current cancer therapies.
Insights
Akt2 signaling is crucial for cancer growth and resistance to chemotherapy. Targeting Akt2 may offer new therapeutic strategies to improve cancer treatment outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Cell Signaling
Background:
- Akt2 is a key regulator of cell growth, proliferation, and survival.
- Aberrant Akt2 signaling contributes to tumor progression, metastasis, and chemoresistance.
- Akt2 is involved in the Phosphat 3 kinase/Akt/Mammalian target of rapamycin (PI3K/mTOR) pathway, regulating metabolism.
Purpose of the Study:
- To investigate the role of Akt2 in cancer, particularly in relation to stem cell-like properties.
- To explore Akt2's involvement in invasiveness and chemoresistance, potentially mediated by Twist.
- To propose therapeutic strategies targeting Akt2 for improved cancer therapy.
Main Methods:
- Signaling pathway analysis
- Cancer cell line studies
- Molecular mechanism investigation
Main Results:
- Akt2 deregulation is linked to tumor progression and chemoresistance.
- Akt2 promotes stem cell-like properties, invasiveness, and chemoresistance, partly via Twist.
- The PI3K/mTOR pathway is implicated in Akt2-driven processes.
Conclusions:
- Akt2 plays a critical role in cancer development and treatment resistance.
- Targeting Akt2, especially in conjunction with pathways like PI3K/mTOR and factors like Twist, presents a promising therapeutic avenue.
- Further research into Akt2 inhibition could lead to overcoming current cancer therapy limitations.
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