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A View of Myeloid Transformation through the Hallmarks of Cancer.
- Source :
-
Blood cancer discovery [Blood Cancer Discov] 2024 Nov 01; Vol. 5 (6), pp. 377-387. - Publication Year :
- 2024
-
Abstract
- The development of myeloid malignancies is influenced by a range of cell-intrinsic and cell-extrinsic factors, which can be conceptualized using the hallmarks of cancer. Although many facets of myeloid transformation are similar to those in solid tumors, there are also notable differences. Unlike solid tumors, hematologic malignancies typically exhibit fewer genetic mutations, which have been well characterized. However, understanding the cell-extrinsic factors contributing to myeloid malignancies can be challenging due to the complex interactions in the hematopoietic microenvironment. Researchers need to focus on these intricate factors to prevent the early onset of myeloid transformation and develop appropriate interventions. Significance: Myeloid malignancies are common in the elderly, and acute myeloid leukemia has an adverse prognosis in older patients. Investigating cell-extrinsic factors influencing myeloid malignancies is crucial to developing approaches for preventing or halting disease progression and predicting clinical outcomes in patients with advanced disease. Whereas successful intervention may require targeting various mechanisms, understanding the contribution of each cell-extrinsic factor will help prioritize clinical targets.<br /> (©2024 American Association for Cancer Research.)
- Subjects :
- Humans
Tumor Microenvironment
Neoplasms pathology
Neoplasms genetics
Leukemia, Myeloid, Acute pathology
Leukemia, Myeloid, Acute genetics
Myeloproliferative Disorders pathology
Myeloproliferative Disorders genetics
Cell Transformation, Neoplastic genetics
Cell Transformation, Neoplastic pathology
Subjects
Details
- Language :
- English
- ISSN :
- 2643-3249
- Volume :
- 5
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Blood cancer discovery
- Publication Type :
- Academic Journal
- Accession number :
- 39422551
- Full Text :
- https://doi.org/10.1158/2643-3230.BCD-24-0009