Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Nina Wietek from the Ahmed lab is investigating fallopian tube tissue to see what we can understand about precancerous mutations in the tissue from which ovarian cancers develops.

Digital render ovarian cancer

High grade serous ovarian cancer (HGSOC) is the most common subtype of ovarian cancer, and is one of the deadliest. Over 80% of these ovarian cancers are detected at an advanced stage, such as stage III or IV, when cancers are much harder to treat. As a result, 10-year survival rates are less than 30% in the UK.

This is despite the fact that HGSOC has a latency period predicted to be between 6.5 and 40 years, whereby a precancerous lesion in the fallopian tube has developed and will go on to become a cancerous tumour. So, despite being present in the body for a long time, current methods are poor at detecting this type of ovarian cancer at an early stage once it has progressed.

This is due in part to a lack of screening techniques for ovarian cancer, such as the very successful screening programmes for other cancers like cervical or colorectal cancer, which have had a considerable impact on patient outcomes over the last decade. Ovarian cancer symptoms are also very non-specific and so make early diagnosis even more challenging, with women often presenting with bloating, abdominal pain, weight loss or weight gain. The precancerous lesions of the fallopian tubes that could develop into serous ovarian cancer are also hard to find due to their small size, and thus are hard to study. There is therefore an urgent need to find new methods of early detection.

Nina Wietek from the Ahmed Lab at the Nuffield Department of Women’s & Reproductive Health is investigating potential avenues for early detection through sequencing tumours and precancerous tissue to explore tumour initiation. To do this Nina is interrogating highly relevant samples obtained directly from patients to gain important insights into tumour development using the power of genomics. Through enhancing our understanding of these early changes, they hope to devise methods of looking for them in order to diagnose ovarian cancer at an early stage, which will have a direct impact on patient survival.

About Nina & the Ahmed lab

Nina Wietek is investigating methods of early detection and prevention of ovarian cancer at the Ahmed Lab. Publications and results from this work is expected later in 2021.

Led by Prof Ahmed Ahmed, the Ovarian Cancer Cell Laboratory in The Weatherall Institute of Molecular Medicine uses cutting-edge innovative technologies to gain deep understanding of mechanistic drivers of ovarian cancer initiation and progression. Find out more about this group here.

Similar Stories

Cancer Science DPhil student named Oxford Sparks Ambassador

Giampiero Valenzano - who is currently reading for a DPhil in Oncology - has been announced as a 2022/2023 Oxford Sparks Ambassador.

Research confirms important differences in colorectal cancer patients with a history of Inflammatory Bowel Disease

IBD-associated colorectal cancers were found to occur in younger patients and have worse outcomes. Researchers call for urgent improvement of early detection methods to provide more risk-based and personalised care.

Public talk: Using blood tests to detect cancer

Organised by the NIHR Oxford Biomedical Research Centre, Professor Mark Middleton and patient representative Sue Duncombe discuss how cancer blood tests are being assessed and how they may change how cancer is diagnosed in the NHS.