News
Comment: Why progress in endometriosis research is urgently needed
By Dr. Zahid Khan, a consultant gynaecologist working in the UAE and CEO of femtech firm, My ANNA Health.
Endometriosis affects an estimated one in 10 women of reproductive age globally—approximately 190 million women. Yet, despite its prevalence, research into this condition has been grossly underfunded and underprioritised.
Recent statistics suggest that only 2 percent of medical research funding is spent on pregnancy, childbirth, and female reproductive health. This is despite one in three women reporting a reproductive or gynaecological health problem.
It is under-researched and underfunded compared to other chronic conditions, contributing to poor diagnostic tools and treatment options. For example, in the U.S., the National Institutes of Health (NIH), the world’s largest source of biomedical research funding, allocated US$41.7bn in 2022.
Despite this, only US$16m – or 0.038 per cent of the NIH budget – was designated for endometriosis research.
Given that endometriosis affects around 11 per cent of US women over their lifetime, this equates to just US$2 per patient per year. In stark contrast, diabetes, which impacts 12 per cent of US women, receives over 1,500 per cent more funding per woman, with an estimated US$31.30 allocated per female patient.
This disparity in funding not only limits our understanding of the disease but also delays the development of effective treatments and diagnostic tools.
An encouraging advancement in the battle against endometriosis is the creation of new AI tools like ANNA (Artificial Narrow Neural Assistant). Designed to aid early diagnosis and reduce the long wait times associated with specialist consultations, ANNA is an AI-driven platform that is being trialled in primary care settings in the UK.
Unlike traditional diagnostic methods that rely on invasive procedures like laparoscopy, ANNA uses a sophisticated algorithm to analyze symptoms and suggest the likelihood of endometriosis. ANNA has been tested with over 160 patients, showing a 100 percent agreement with specialist diagnoses, a clear indicator of its potential in revolutionizing early diagnosis.
ANNA is multilingual and designed with a culturally sensitive avatar, breaking down language barriers and providing healthcare access to women from diverse backgrounds. It can be used independently by patients or in consultation with healthcare professionals, guiding them on when to seek specialist help and offering pain management strategies. By integrating ANNA into primary care, the timeline for diagnosis can be significantly shortened, allowing women to receive timely treatment and improve their quality of life.
Research into and adoption of non-invasive diagnostic tools, like ANNA, is critical to reducing the years of suffering that many women endure. Beyond diagnosis, we need to focus on better treatment options that go beyond hormonal therapies and surgery.
These treatments often have severe side effects, and in many cases, they aren’t curative. Research into the causes of endometriosis—whether genetic, hormonal-, or immunological—will pave the way for more targeted therapies that address the disease at its source.
The importance of awareness cannot be overstated. Primary care providers need to be better trained to recognise the symptoms of endometriosis early on. Public health campaigns should inform women about what constitutes normal menstruation and when they should seek help. Too many women suffer in silence, told by doctors that their pain is “normal” or dismissed with misdiagnoses.
Abu Dhabi is investing in making real changes, developing these cutting-edge surgical techniques for endometriosis and setting up efficient specialized care centers. At our Centre of Excellence, we perform six to seven endometriosis surgeries a week, with recurrence rates below 9 percent.
These are promising advancements, but the next challenge is scaling up these technologies and advancements, ensuring that they are accessible to women worldwide.
Diagnosis
Lung cancer drug shows breast cancer potential
Ovarian cancer cells quickly activate survival responses after PARP inhibitor treatment, and a lung cancer drug could help block this, research suggests.
PARP inhibitors are a common treatment for ovarian cancer, particularly in tumours with faulty DNA repair. They stop cancer cells fixing DNA damage, which leads to cell death, but many tumours later stop responding.
Researchers identified a way cancer cells may survive PARP inhibitor treatment from the outset, pointing to a potential way to block that response. A Mayo Clinic team found ovarian cancer cells rapidly switch on a pro-survival programme after exposure to PARP inhibitors. A key driver is FRA1, a transcription factor (a protein that turns genes on and off) that helps cancer cells adapt and avoid death.
The team then tested whether brigatinib, a drug approved for certain lung cancers, could block this response and boost the effect of PARP inhibitors. Brigatinib was chosen because it inhibits multiple signalling pathways involved in cancer cell survival.
In laboratory studies, combining brigatinib with a PARP inhibitor was more effective than either treatment alone. Notably, the effect was seen in cancer cells but not normal cells, suggesting a more targeted approach.
Brigatinib also appeared to act in an unexpected way. Rather than working through the usual DNA repair routes, it shut down two signalling molecules, FAK and EPHA2, that aggressive ovarian cancer cells rely on. FAK and EPHA2 are proteins that relay survival signals inside cells. Blocking both at once weakened the cells’ ability to adapt and resist treatment, making them more vulnerable to PARP inhibitors.
Tumours with higher levels of FAK and EPHA2 responded better to the drug combination. Other data link high levels of these molecules to more aggressive disease, pointing to potential benefit in harder-to-treat cases.
Arun Kanakkanthara, an oncology investigator at Mayo Clinic and a senior author of the study, said: “This work shows that drug resistance does not always emerge slowly over time; cancer cells can activate survival programmes very early after treatment begins.”
John Weroha, a medical oncologist at Mayo Clinic and a senior author of the study, said: “From a clinical perspective, resistance remains one of the biggest challenges in treating ovarian cancer. By combining mechanistic insights from Dr Kanakkanthara’s laboratory with my clinical experience, this preclinical work supports the strategy of targeting resistance early, before it has a chance to take hold. This strategy could improve patient outcomes.”
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