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Wnt signalling in gynaecological cancers: A future target for personalised medicine?
C E Ford1, C Henry1, E Llamosas1
1Metastasis Research Group, Prince of Wales Clinical School, Lowy Cancer Research Centre, University of New South Wales, Australia.
Abstract:
The three major gynaecological cancers, ovarian, uterine and cervical, contribute a significant burden to global cancer mortality, and affect women in both developed and developing countries. However, unlike other cancer types that have seen rapid advances and incorporation of targeted treatments in recent years, personalised medicine is not yet a reality in the treatment of gynaecological cancers. Advances in sequencing technology and international collaborations and initiatives such as The Cancer Genome Atlas are now revealing the molecular basis of these cancers, and highlighting key signalling pathways involved. One pathway which plays a role in all three cancer types, is the Wnt signalling pathway. This complex developmental pathway is altered in most human malignancies, and members of this pathway, particularly the recently linked ROR receptor tyrosine kinases may be attractive future therapeutic targets. This review provides an up-to-date summary of research into Wnt signalling and ovarian, uterine and cervical cancers, and discusses the potential of the Wnt pathway as a future target for personalised medicine in gynaecological cancers.
Insights
Personalized medicine remains elusive for ovarian, uterine, and cervical cancers. The Wnt signalling pathway presents a promising therapeutic target for these gynaecological malignancies.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Gynaecological cancers (ovarian, uterine, cervical) represent a significant global health burden.
- Personalized medicine approaches are lacking in gynaecological cancer treatment.
- Recent advances reveal the molecular underpinnings of these cancers, identifying key signaling pathways.
Purpose of the Study:
- To review current research on the Wnt signaling pathway in ovarian, uterine, and cervical cancers.
- To explore the potential of the Wnt pathway as a therapeutic target for personalized medicine in gynaecological oncology.
Main Methods:
- Literature review of Wnt signaling pathway research in gynaecological cancers.
- Analysis of molecular data from initiatives like The Cancer Genome Atlas.
- Identification of potential therapeutic targets within the Wnt pathway, including ROR receptor tyrosine kinases.
Main Results:
- The Wnt signaling pathway is implicated in all three major gynaecological cancers.
- Alterations in the Wnt pathway are common in human malignancies.
- ROR receptor tyrosine kinases are emerging as potential therapeutic targets within this pathway.
Conclusions:
- The Wnt signaling pathway is a critical player in gynaecological cancers.
- Targeting the Wnt pathway offers a potential avenue for developing personalized treatments.
- Further research into Wnt pathway modulators could revolutionize gynaecological cancer therapy.
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