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Phase transition inside the nucleus provides oncogenic function to mutant p53 in cancer


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IMAGE: Pathway of mutant p53 from liquid droplets to gel-like and solid-like (amyloid) states, in vitro and in cell.
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Credit: Guilherme de Oliveira
Cancer has been recently shown to be affected by protein clusters, particularly by the aggregation of mutant variants of the tumor suppressor protein p53, which are present in more than half of malignant tumors. However, how the aggregates are formed is not yet fully understood. The understanding of this process is expected to provide new therapeutic tools able to prevent proteins to clump and cancer progression.
In Brazil, researchers at the Federal University of Rio de Janeiro have identified a key mechanism behind the mutant p53 aggregation process, linked to cancer pathology, opening new paths for the development of novels drugs against the disease. ....

Rio De Janeiro , Estado Do Rio , Fernandop Almeida , Adrianil Felix , Yullim Passos , Yraima Cordeiro , Mayraa Marques , Michellef Mota , Giuliads Ferretti , Benjamin Jakobus , Tuane Vieira , Murilom Pedrote , Elainec Petronilho , Technology For Structural Biology , Technological Development Cnpq , Royal Society Of Chemistry , National Institute Of Science , University Of Rio De Janeiro , National Council For Scientifc , Carlos Chagas Filho Foundation For Research , Federal University , Chemical Science , Royal Society , Jerson Lima Silva , Lima Silva , Santos De Sousa ,