{"id":4904,"date":"2020-02-20T00:00:00","date_gmt":"2020-02-19T23:00:00","guid":{"rendered":"https:\/\/idibell.cat\/en\/blog\/2020\/05\/01\/new-results-on-the-function-of-the-tumor-suppressor-herc-protein\/"},"modified":"2020-05-28T09:42:15","modified_gmt":"2020-05-28T07:42:15","slug":"new-results-on-the-function-of-the-tumor-suppressor-herc-protein","status":"publish","type":"post","link":"https:\/\/idibell.cat\/en\/2020\/02\/new-results-on-the-function-of-the-tumor-suppressor-herc-protein\/","title":{"rendered":"New results on the function of the tumor suppressor HERC protein"},"content":{"rendered":"
The RAF protein could be a therapeutical target to treat the tumor growth in regulated pathways by the p38 protein, according to a new study published in the journal\u00a0Scientific Reports<\/a>\u00a0by a team of experts of the Faculty of Medicine and Health Sciences of the UB and the Bellvitge Institute for Biomedical Research (IDIBELL). The study analyzes the mechanisms that regulate some molecular signaling pathways related to carcinogenesis and tumor progression and opens new perspectives to the fight against human cancer.<\/p>\n Among the participants in the new study, led by Professor Jos\u00e9 Luis Rosa, are the researchers Leonardo Pedrazza, Taiane Schneider, Ramon Bartrons and Francesc Ventura, from the Department of Physiological Sciences of the UB and IDIBELL.<\/p>\n <\/p>\n <\/p>\n The p38 protein, which belongs to the family of mitogen-activated kinase (MAP or MAPK kinase), is a factor with a distinguished role in the response to cellular stress signals and the control of proliferation and progress of tumor cells.<\/p>\n MAPK proteins and the regulator kinases \u2013MAPKK and MAPKKK\u2013 take part in intracellular signaling cascades such as the RAF\/MEK\/ERK pathway, which controls the essential cell processes (growth, proliferation, differentiation, survival and cell migration). Dysfunctions in the regulation of these molecular signaling pathways can alter the physiological cycle of the cell and therefore generate the tumor proliferation and growth.<\/p>\n The published study in the journal\u00a0Scientific Reports\u00a0describes for the first time how the HERC1 enzyme \u2013ubiquitin ligase- is able to regulate the process of cell migration through the MKK\u00b7\/p38 signaling pathway, regulated by the C-RAF factor.\u00a0The new study expands the knowledge on the tumor-suppressor role of HERC proteins (ubiquitin ligase); enzymes that regulate the function of some proteins involved in processes such as cell growth and proliferation through its molecular marking with ubiquitin molecules (ubiquitination). In particular, the new study reveals HERC1 ligase i sable to regulate the activation of ERK and p38 kinase through the union of ubiquitin molecules with the C-RAF factor.<\/p>\n According to the authors, the discovery of an unexpected communication between RAF proteins and MKK3\/p38 pathway opens new perspectives regarding future therapeutical targets in the fight against human cancers.<\/p>\n Moreover, the research group has a distinguished experience in the study of HERC proteins and their link to several pathologies (cancer, ataxia, etc.). In previous studies, the team contributed to the functional characterization of two ubiquitin kinases \u2013HERC1 and HERC2 (Frontiers in Oncology,<\/a>\u00a02019)\u2014 and the description of the role of HERC1 ligase in the regulation of the cell proliferation through the activation of the ERK signaling pathway through a mechanism that affects ubiquitination and degradation of C-RAF (Oncotarget<\/a>, 2018).<\/p>\n <\/p>\n <\/p>\nHow does HERC1 ligase regulate the activation of ERK and p38 kinase?<\/h4>\n
HERC2 ligase and regulation of p5 protein, tumor suppressor<\/h4>\n