ANXO
VIDAL FIGUEROA

Anxo Vidal received his Ph.D. in Cell Biology in 1997 at the University of Santiago de Compostela. From 1998 to 2003 he was a postdoc at Memorial Sloan-Kettering Cancer Center. Anxo’s research interests were the study of p27Kip1 regulation and the genetic and functional relationships among tumor suppressors. In 2002 he was ranked no. 2 nationwide in the area of Physiology in the “Ramon y Cajal” Program. Back in Santiago de Compostela in 2003, he established his own laboratory devoted to study cell cycle and tumor biology through mouse models. Since 2008, Anxo is an Associate Professor of Physiology in the University of Santiago de Compostela. Anxo was the recipient of the 2006 Novartis Award in Endocrine Tumor Pathology. Invited speaker at several national and foreign research centers. Principal investigator of competitive national and international grants, he is an author of around 70 international publications in high visibility journals (Nature Communications, Cell Stem Cell, Nature Neuroscience, Adv Func Mater…), with an h-index of 32 (Scopus, September 2025) and a relative citation ratio of 1,53 (iCite, September 2025). He is an author also of four international patents and has supervised 16 PhD thesis. Main contributions to research are summarized as follows: 1. Mechanisms of p27Kip1 translational regulation: My research during my postdoctoral stage at MSKCC focused on how levels of p27Kip1 (a cell cycle inhibitor and a tumor suppressor) are regulated. I was involved in the characterization of 'cis' elements on p27 mRNA important for its translation, the isolation of proteins that bind those sites as well as the delineation of signalling pathways involved (Millard et al MCB 2000; Vidal et al JBC 2002). 2. New cooperative functions of cell cycle regulators: In contrast to biochemical and cellular approaches, genetic mouse models have provided light to overlapping and redundant “in vivo” roles of cell cycle inhibitors. Having established my own group at USC my work has contributed to discover new cooperative functions of cell cycle regulators in angiogenesis (Vidal et al, PNAS 2005) and endochondral bone formation (Yeh et al, MCB 2007). 3. Cell cycle independent roles of cdk-inhibitors in cancer, stem cell biology and aging: For many years, the only attributed functions of cdk inhibitors (mainly p21Cip and p27Kip1) were to bind to and to inhibit cdk kinases. In collaboration with others my group has made fundamental contributions to show how these cdk inhibitors work as transcriptional regulators, a function which is essential for embryonic and adult stem cell biology, but also for their role as tumor suppressors (Li et al Cell Stem Cell 2012; Marques-Torrejon et al Cell Stem Cell 2013; Porlan et al Nat Neurosci 2013). In continuation with our previous findings, work form my group has contributed to establish how cell cycle regulators control expression of reprogramming factors, and how this impinges on tumor initiation and development, but also in tissue homeostasis maintenance and hence in aging (Vilas et al Oncotarget 2015; Vilas et al Aging Cell 2018; Ferreiros et al Stem Cell Reports 2019; Lado-Fernández et al Int J Cancer 2025) 4. New therapeutic tools in advanced cancer: In recent years, our group explores new therapeutic strategies in cancer using nanomedicines (Amaral et al Angew Chem 2018; Teijeiro-Valiño et al J Control Rel 2019; Goldberg et al Nat Commun 2022). Work from my lab has contributed to establish that drug nanocarriers represent a promising therapy for the treatment of advanced lung metastatic cancer (Borrajo et al J Control Rel 2016) to test new materials as therapeutic tools in cancer (Porto et al Adv Func Mater 2022), and to explore new biological therapies (McDonald et al Mol Oncol 2025, López-Estévez et al J Control Rel 2025)