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Updated: Jun 20, 2026

Tropomodulin 3 Overexpression as a Marker for Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
TrkB as a therapeutic target for ovarian cancer
Michelle K Y Siu1, Oscar G W Wong, Annie N Y Cheung
1The University of Hong Kong, Queen Mary Hospital, Department of Pathology, Hong Kong, China.
Background:
In many countries, ovarian cancer is the most lethal gynecological malignancy. Its poor prognosis is mainly due to the late stage of disease with metastasis at presentation. The significant failure rate of chemotherapy in patients with advanced stage disease is also a main concern. As such, developing novel therapeutic targets is essential to improve long-term survival. Overexpression of Tropomyosin-related kinase B (TrkB), a tyrosine kinase receptor, has been documented in ovarian cancer and is found to be correlated with poor prognosis.
Objective/Methods:
We discuss the functional roles and the related downstream signaling pathways of TrkB and its ligand brain-derived neurotrophic factor (BDNF) in ovarian cancer. The possible crosstalk between TrkB/BDNF and other putative molecular targets in ovarian cancer is also discussed.
Results/Conclusions:
All these latest findings shed light on the application of TrkB as a therapeutic target for ovarian cancer.
Insights
Tropomyosin-related kinase B (TrkB) is overexpressed in ovarian cancer, correlating with poor prognosis. Targeting TrkB and its ligand, brain-derived neurotrophic factor (BDNF), offers a promising therapeutic strategy for this lethal gynecological malignancy.
Area of Science:
- Gynecologic Oncology
- Molecular Oncology
- Cancer Signaling
Background:
- Ovarian cancer is a leading cause of cancer death globally, often presenting with metastasis and resistance to chemotherapy.
- Poor prognosis in ovarian cancer is linked to late-stage diagnosis and treatment failure.
- Overexpression of Tropomyosin-related kinase B (TrkB), a receptor tyrosine kinase, is observed in ovarian cancer and associated with adverse outcomes.
Purpose of the Study:
- To review the functional roles of TrkB and its ligand, brain-derived neurotrophic factor (BDNF), in ovarian cancer.
- To elucidate the downstream signaling pathways influenced by TrkB/BDNF in ovarian cancer.
- To explore potential crosstalk between the TrkB/BDNF pathway and other molecular targets in ovarian cancer.
Main Methods:
- Literature review of studies investigating TrkB and BDNF in ovarian cancer.
- Analysis of signaling pathways downstream of TrkB activation.
- Examination of potential therapeutic targeting strategies.
Main Results:
- TrkB and BDNF play significant roles in ovarian cancer progression and survival.
- Specific downstream signaling cascades activated by TrkB/BDNF contribute to tumorigenesis.
- Interactions between TrkB/BDNF and other molecular pathways are implicated in ovarian cancer.
Conclusions:
- The TrkB receptor and its ligand BDNF are critical players in ovarian cancer.
- Targeting the TrkB/BDNF pathway presents a viable therapeutic avenue.
- Further research into TrkB as a therapeutic target could improve patient survival in ovarian cancer.
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