Cancer and rare genetic disorders are an emerging area of research, as certain rare genetic conditions predispose individuals to specific types of cancer. Syndromes such as Li-Fraumeni syndrome, Lynch syndrome, and Fanconi anemia, which are caused by inherited mutations in tumor suppressor genes or repair genes, increase the risk of developing a variety of cancers at an early age. Cancer research is focused on identifying the genetic mutations that contribute to these rare disorders and understanding how they promote cancer development. Researchers are also looking into precision therapies that target the underlying genetic defects, which could provide more effective treatments for individuals with rare genetic disorders and their associated cancers.
Title : A novel blood-based mRNA genomics technology for cancer diagnosis and treatment
Rajvir Dahiya, University of California San Francisco, United States
Title : tRNA-derived fragment 3′tRF-AlaAGC modulates cell chemoresistance and M2 macrophage polarization via binding to TRADD in breast cancer
Feng Yan, The Affiliated Cancer Hospital of Nanjing Medical University, China
Title : Integrating single-cell and spatial transcriptomics to uncover and elucidate GP73-mediated pro-angiogenic regulatory networks in hepatocellular carcinoma
Jiazhou Ye, Guangxi Medical University Cancer Hospital, China
Title : Unveiling the synergism of radiofrequency therapy and graphene nanocomposite in tumor cell viability assay
Paulo Cesar De Morais, Catholic University of Brasilia, Brazil
Title : Analysis of the dynamic evolution and influencing factors of nutritional risk in breast cancer patients during treatment
Jingwen Yan, Sun Yat-sen University, China
Title : Integrative multi-omics reveals metabolic–stemness coupling and novel therapeutic targets in osteosarcoma chemoresistance
Jinyan Feng, Tianjin Medical University Cancer Institute and Hospital, China