Dr. Asem Mansour, Dr. Amal Al Omari and Dr. Omar El Agnaf
Doha: Qatar Biomedical Research Institute (QBRI) – part of Qatar Foundation member Hamad Bin Khalifa University and the King Hussain Cancer Center (KHCC) in Jordan, together with Hamad Medical Corporation (HMC), have launched a strategic initiative aimed at developing a better understanding of breast cancer complexity in the Arab region, employing cutting-edge technologies and engaging scientists and clinicians with varied expertise.
Regionally, breast cancer is the most common cancer among women accounting for approximately 30 percent of female cancer cases in Qatar and the MENA region, meaning it represents a major health burden.
The chief goal of the Qatar-Jordan collaboration is to discover novel susceptibility genes in the Arab population which could help to identify and monitor families with a high genetic risk of developing breast cancer; and to enable prevention, early detection, and treatment, improve breast cancer patients’ prospects of surviving the condition. It could also lead to more personalized treatment for patients, by allowing the most appropriate therapy to be selected based on their genetic background.
Chief Scientific Officer at KHCC, Dr. Amal Al Omari, “Breast cancer is still the most common malignancy among women worldwide and constitutes a significant percentage of all cancer cases diagnosed in Arab females.
“Breast cancer in Arab women is also characterized by distinctive features, such as the younger age at the point of diagnosis compared to Western countries. Today, our understanding of disease mechanisms and gene functions enables us to guide treatment strategies and design medical interventions that are appropriate to the individual patient’s needs and assess the extent of the response to these targeted interventions.”Among the well-known familial breast cancer risk factors are mutations in the BRCA1 and BRCA2 genes, which account for only 10-20 percent of high-risk cancer cases. This means the genetic driver behind other high-risk familial breast cancer phenotypes in the MENA region remain unidentified.
As a first step towards identification of those driver genes, QBRI has received the first batch of genomic DNA from patients with familial breast cancer not related to BRCA1 and BRCA2 mutations from KHCC. Those samples have undergone whole genome sequencing, with the data currently being analyzed. Initial analysis of those samples has revealed the presence of large number of genetic alterations.
Through complex computational algorithms, scientists at QBRI are currently working to decipher genetic data to identify novel susceptibility driver genes beyond BRCA1 and BRCA2. They are doing this by analyzing additional samples from KHCC while also integrating data from Qatari patients though the collaboration with HMC, to provide a wider picture of genomic alterations in breast cancer patients from the MENA region.
Executive Director of QBRI, Dr. Omar El Agnaf said, “Breast cancer can be a result of different underlying genetic causes, and this variability lends itself to the growing field of precision medicine, which can result in immense patient benefits.
Chief Executive Officer and Director General of KHCC, Dr. Asem Mansour, said, “There is great optimism for this unique scientific cooperation between the exceptional research capabilities of Qatar Biomedical Research Institute and the distinguished medical and research expertise at the King Hussein Cancer Center. He said “We hope that, in the near future, there will be a transformation in healthcare and diagnostic technology in the Arab world."
