Publications by authors named "Sanaa El Marsafy"

Tumor recurrence is a colossal challenge in clinical oncology. This multifactorial problem is attributed to the emergence of additional genetic mutations and the presence of dormant cancer cells. However, the plasticity of non-stem cancer cells and the acquisition of cancer stem cell (CSC) functionality is another contributing factor to tumor recurrence.

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Article Synopsis
  • - The study utilizes whole-genome sequencing (WGS) to analyze a patient with chronic myeloid leukemia, tracking changes over 9 years from chronic phase to blast phase, revealing significant mutations and clonal dynamics.
  • - WGS identified multiple mutations, including ASXL1 and SEC23B, along with 12,000 rare DNA variants, indicating a complex genetic landscape within the patient's CML cells.
  • - The research suggests that current understandings of clonal evolution in CML may need reevaluation, as similar mutations appeared in other cases of myeloproliferative neoplasms but not in healthy individuals.
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Tumors grow in privileged microenvironment referred to as the cancer niche. This niche is composed of cancer cells and various components including mesenchymal stem cells (MSC), fibroblasts, network of microvasculature added to innate and primed immune cells. Additionally, it encloses other elements such as the extracellular matrix (ECM), cytokines, chemokines and growth factors.

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Melanoma is an aggressive malignancy with poor prognosis. Eradication of tumor cells requires an effective interaction between melanoma cells and different players of the immune system. As the most potent professional antigen-presenting cells, dendritic cells (DCs) play a pivotal role in mounting a specific immune response where their intratumoral and peritumoral density as well as their functional status are correlated with clinical staging of the disease and with patients' survival.

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