Kimaya Das
This research paper focuses on gene expression in Pediatric Acute Myeloid Leukemia (AML) as well as discovering genes that are linked to chemotherapy resistance in AML.Â
This research paper focuses on gene expression in Pediatric Acute Myeloid Leukemia (AML) as well as discovering genes that are linked to chemotherapy resistance in AML.Â
Acute Myeloid Leukemia (AML) is a dangerous type of blood cancer that is common in both adults and children. This research paper offers a revealing glimpse into the genetic landscape of pediatric AML that does not respond to initial chemotherapy. This study is a step toward understanding the stubborn nature of certain leukemias and paves the way for personalized therapeutic strategies. AML in children often presents a challenging battle due to its genetic complexity and the potential for resistance to standard chemotherapy treatments. The goal is to identify potential genetic targets for improving treatment efficacy and patient outcomes in this challenging subset of AML. To accomplish this goal, high throughput sequencing analysis was employed to examine the gene expression profiles of bone marrow samples collected from pediatric AML patients who did not respond to initial chemotherapy. This approach allowed the scientists to identify and characterize the genetic mutations associated with treatment resistance. While this study seeks to unravel the genetic factors that underlie the resistance of pediatric AML to first-line chemotherapy, there was a focus on the role of NUP98, WT1, and FRMD8 gene expressions. Specifically, the researchers found that these genetic alterations disrupt normal gene expression pathways, which may contribute to the disease's persistence despite treatment. Understanding the gene expression patterns provides valuable insights into the underlying mechanisms of leukemia development and chemotherapy resistance. This knowledge can potentially lead to the development of targeted therapies that can improve treatment outcomes for patients with AML.
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