Cancer genetics and genomics is a rapidly evolving field that focuses on understanding the genetic mutations and alterations that contribute to the development and progression of cancer. By studying the genetic makeup of both normal and cancerous cells, researchers are uncovering the underlying mechanisms that drive tumor formation. This knowledge is crucial for identifying specific biomarkers for early diagnosis, predicting treatment responses, and developing personalized therapies. Advances in genomic technologies, such as next-generation sequencing, have made it possible to analyze cancer genomes in unprecedented detail, paving the way for targeted therapies that can more effectively treat various types of cancer.
Title : A novel blood-based mRNA genomics technology for cancer diagnosis and treatment
Rajvir Dahiya, University of California San Francisco, United States
Title : Uncovering tumor-suppressive roles of histone modifiers in gastric cancer through spatial transcriptomics and epigenomics
Shilpa S Dhar, UT MD Anderson Cancer Center, United States
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 : A case-based approach using IMPeTUs criteria in FDG PET/CT reporting of multiple myeloma
Mudalsha Ravina, All India Institute of Medical Sciences, India
Title : Transforming cancer care: Innovations, integrations, and impact
Shayan Maqsood, Jamia Hamdard University, India
Title : Updates on controversies surrounding the staging and management of newly diagnosed localized prostate cancer using prostate-specific membrane antigen (PSMA) positron emission tomography
Patricia Tai, University of Saskatchewan, Canada