Researchers at the IMIM (Institut de Recerca Hospital del Mar) have proven that the absence of the 14-3-3 protein sigma in breast cancer cells is directly associated with these cells’ capacity to activate the signaling of a protein complex called NF-kB, which is related to tumor progression.
The activation of NF-kB in tumors was also identified as the best indicator for relapse in breast cancer patients, compared to other parameters currently used, such as the presence of affected ganglions or the tumor’s size and degree. The investigators have also described a group of genes that are activated in breast cancer cells and that are also associated with a poor prognosis in other types of tumors.
Previous studies had detected that the 14-3-3 protein sigma was not present in the tumors of many breast cancer patients. They have now discovered that “the lack of this protein does not in itself establish a prognosis factor for these types of cancer, although the NF-kB complex is an essential requirement for it to remain active chronically, as it is associated with tumor invasion and metastasis or, stated differently, the progression of the tumor,” comments Luís Espinosa, study coordinator and researcher in the IMIM stem cells and cancer research group.
Breast cancer is most common among women in Western countries and relapse and metastasis are the fatal consequences of this disease. Identifying the mechanisms involved in the survival of breast cancer cells and their ability to colonize other tissues are crucial issues for improving treatment. With the participation of some 100 patients, this study analyzed the possible usefulness of determining the lack of the 14-3-3 sigma and/or the activation of NF-kB in tumor cells as a factor in prognosis and diagnosis, as well as for future clinical and therapeutic applications.
The results obtained from this project have opened up new roads of investigation that will have to center on identifying the pharmaceuticals that induce the expression of the 14-3-3 protein sigma in breast tumors and characterize their effect on tumor cells. They also hope to define which genes activated by the NF-kB complex are important for tumor progression in this group of patients and to study their potential as possible therapeutic targets.
According to Espinosa, “This opens up the possibility of researching and employing specific therapeutic strategies for this concrete group of patients who, in principle, have bad prognoses and an especially high risk of relapse.”
PloS One, May 31, 2012
Institut de Recerca Hospital del Mar (http://www.imim.es)