DOI: 10.37421/2577-0535.2024.9.243
Breast cancer, a complex and varied disease affecting millions worldwide, poses a considerable treatment challenge due to its ability to evolve and adapt. Examining the intricate alterations within the breast cancer genome over time provides essential understanding of tumor evolution, treatment resistance and the tailoring of therapies. This piece explores the dynamic characteristics of breast cancer genomes, shedding light on the methods used to unravel their evolutionary trajectories.
DOI: 10.37421/2577-0535.2024.9.24
DOI: 10.37421/2577-0535.2024.9.246
DOI: 10.37421/2577-0535.2024.9.245
Protein Tyrosine Phosphatase PRL-3 (PTP4A3), belonging to the PRL family, has surfaced as a noteworthy participant in cancer signaling routes. Its irregularities have been linked to multiple phases of cancer advancement, such as metastasis and angiogenesis. This piece explores the architecture, operation, control, and medical relevance of PRL-3, illuminating its prospects as a target for cancer therapy.
DOI: 10.37421/2577-0535.2024.9.244
DOI: 10.37421/2577-0535.2024.9.242
DOI: 10.37421/2577-0535.2024.9.241
DOI: 10.37421/2577-0535.2024.9.240
DOI: 10.37421/2577-0535.2024.9.239
An ultrasensitive DNA-biomacromolecule system or technology can detect and analyze DNA molecules with exceptional precision. As the fundamental genetic material in living organisms, DNA is crucial for numerous biological processes and has extensive applications in diagnostics and research. These ultrasensitive technologies are designed to identify and quantify tiny amounts of DNA within a sample. Utilizing various detection methodologies such as fluorescence, electrochemical sensing, nanopore sequencing, or amplification techniques like polymerase chain reaction, these technologies allow scientists to achieve highly accurate and sensitive detection of DNA molecules, even at extremely low concentrations.
DOI: 10.37421/2577-0535.2024.9.238
Pancreatic Ductal Adenocarcinoma is among the most lethal cancers, characterized by limited treatment options and poor prognosis. Its hallmark resistance to conventional therapies necessitates the exploration of targeted therapeutic approaches. Recent advances have significantly deepened our understanding of the oncogenic pathways driving PDAC development and progression. This article reviews clinical and preclinical strategies targeting these pathways, highlighting promising avenues for treating this deadly cancer.
Journal of Cancer Clinical Trials received 95 citations as per Google Scholar report