Oxidative stress stimulates p38 MAPK-mediated tumor suppression
The MAPK p38-alpha is a signaling protein that plays a critical role in coordinating cellular responses to stress, including oxidative stress that is characterized by the accumulation of increased levels of reactive oxygen species (ROS) within the cell. Although the p38-alpha pathway has been implicated in tumor suppression, the mechanisms involved are not well understood. Dr. Angel R. Nebreda from CNIO (Spanish National Cancer Center) in Madrid and colleagues induced malignant transformation in cells from mice lacking p38-alpha and in wild-type cells to study the importance of p38-alpha in tumorigenesis.
The deficiency of p38-alpha caused increased cell proliferation, decreased cell death via apoptosis, and enhancement of other characteristics associated with malignancy. Importantly, reintroduction of p38-alpha to the deficient cells reversed this phenotype. The researchers observed that the transformed cells lacking p38-alpha had much higher ROS levels than the wild-type cells. Further, ROS-stimulated p38-alpha activity in the wild-type cells stimulated apoptosis, whereas the cells lacking p38-alpha were resistant to ROS-induced apoptosis. The researchers point out that this finding may have clinical significance, as they observed that increased ROS levels were also linked to tumorigenic potential in several human cancer cell lines that were examined.
The authors suggest that it may be possible for cancer cells to escape the tumor-suppressive functions of p38-alpha by desensitizing p38-alpha to oxidative stress. Indeed, many tumor cells exhibit increased expression of GST proteins that are known to specifically inhibit p38-alpha activation by ROS. Reduced expression of GST in cancer cells correlated with increased p38-alpha activity and apoptosis, while enhanced expression of GST led to reduced p38-alpha activation, higher ROS levels, and enhanced malignancy of cancer cells.
Taken together, the findings suggest that p38-alpha plays a critical role in the negative regulation of tumor formation by triggering apoptosis in response to oncogene-induced ROS accumulation and that cancer cells may elude this protective mechanism by uncoupling ROS from p38-alpha. “Our results illustrate a mechanism used by cancer cells for the inactivation of tumor suppressor pathways and suggest that restoring the ROS-induced activation of p38 MAPK, for example, by targeting GST proteins, may be of potential therapeutic interest,” concludes Dr. Nebreda.
Alle Nachrichten aus der Kategorie: Life Sciences
Articles and reports from the Life Sciences area deal with applied and basic research into modern biology, chemistry and human medicine.
Valuable information can be found on a range of life sciences fields including bacteriology, biochemistry, bionics, bioinformatics, biophysics, biotechnology, genetics, geobotany, human biology, marine biology, microbiology, molecular biology, cellular biology, zoology, bioinorganic chemistry, microchemistry and environmental chemistry.
New approach to fighting cancer could reduce costs and side effects
CAR-T biotherapeutics company Carina Biotech and researchers at the University of South Australia have developed a novel approach based on microfluidic technology to “purify” the immune cells of patients in…