Emerging treatment options for patients with p53-pathway-deficient CLL.
Marisa J L AitkenHun J LeeSean M PostPublished in: Therapeutic advances in hematology (2019)
Over the past 40 years, p53 has been the most widely studied protein in cancer biology. Originally thought to be an oncogene due to its stabilization in many cancers, it is now considered to be one of the most critical tumor suppressors in a cell's ability to combat neoplastic transformation. Due to its critical roles in apoptosis, cell-cycle arrest, and senescence, TP53 deletions and mutations are commonly observed and are often a portent of treatment failures and poor clinical outcomes. This is particularly true in chronic lymphocytic leukemia (CLL), as patients with p53 alterations have historically had dismal outcomes. As such, the tremendous efforts made to better understand the functions of p53 in CLL have contributed substantially to recent advances in treating patients with p53-pathway-deficient CLL.
Keyphrases
- chronic lymphocytic leukemia
- cell cycle arrest
- cell death
- pi k akt
- oxidative stress
- dna damage
- single cell
- signaling pathway
- papillary thyroid
- endoplasmic reticulum stress
- endothelial cells
- stem cells
- cell therapy
- cell proliferation
- squamous cell
- squamous cell carcinoma
- quality improvement
- adipose tissue
- metabolic syndrome
- insulin resistance
- small molecule
- combination therapy
- lymph node metastasis
- smoking cessation