Next-generation sequencing (NGS) has become a cornerstone in oncology research, offering unprecedented insights into the molecular architecture of cancers. This advanced technology allows for a detailed examination of the genetic mutations, variations, and alterations that drive tumor growth. By sequencing the DNA or RNA of cancerous tissues, clinicians can identify specific mutations, enabling personalized treatment options tailored to the individual’s genetic makeup. NGS is also valuable in detecting rare genetic mutations that may not be visible with conventional methods, allowing for early diagnosis and more targeted therapies. As a result, it plays a crucial role in precision medicine, offering hope for more effective treatments and improved patient outcomes.
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