Mireia Niso-Santano

Dr. Mireia Niso-Santano

1. Department Bioquímica y Biología Molecular y Genética, Facultad de Enfermería y Terapia Ocupacional, Universidad de Extremadura Avda de la Universidad s/n, 10003 Cáceres, Spain
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Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 January 2014 in Nature Reviews Molecular Cell Biology
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Journal Article
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Guillermo MariñoGuillermo Mariño
Guillermo Mariño
MNMireia Niso-Santano
Mireia Niso-Santano
EBEric H. Baehrecke
Eric H. Baehrecke
Guido KroemerGuido Kroemer
Guido Kroemer

26 October 2014 in Nature Medicine
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Journal Article
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Antonella SistiguAntonella Sistigu
Antonella Sistigu
TYTakahiro Yamazaki
Takahiro Yamazaki
EVErika Vacchelli
Erika Vacchelli
KCKariman Chaba
Kariman Chaba
DEDavid P Enot
David P Enot
LZLaurence Zitvogel
Laurence Zitvogel

1 March 2014 in Molecular Cell
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Journal Article
Closed access
Guillermo MariñoGuillermo Mariño
Guillermo Mariño
FPFederico Pietrocola
Federico Pietrocola
Tobias EisenbergTobias Eisenberg
Tobias Eisenberg
YKYongli Kong
Yongli Kong
SMShoaib Ahmad Malik
Shoaib Ahmad Malik
Guido KroemerGuido Kroemer
Guido Kroemer

28 September 2012 in Science
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Journal Article
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LSLaura SENOVILLA
Laura SENOVILLA
IVIlio Vitale
Ilio Vitale
IMIsabelle Martins
Isabelle Martins
MTMaximilien Tailler
Maximilien Tailler
CPClaire Pailleret
Claire Pailleret
Guido KroemerGuido Kroemer
Guido Kroemer
Keeping Cancer Cells At Bay: Cancer cells are often aneuploid; that is, they have an abnormal number of chromosomes. But to what extent this contributes to the tumorigenic phenotype is not clear. Senovilla et al. (p. 1678 ; see the Perspective by Zanetti and Mahadevan ) found that tetraploidization of cancer cells can cause them to become immunogenic and thus aid in their clearance from the body by the immune system. Cells with excess chromosomes put stress on the endoplasmic reticulum, which leads to movement of the protein calreticulin to the cell surface. Calreticulin exposure in turn caused recognition of cancer cells in mice by the host immune system. Thus, the immune system appears to serve a protective role in eliminating hyperploid cells that must be overcome to allow unrestricted growth of cancer cells.

19 December 2014 in Cell Death & Differentiation
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Journal Article
Open access
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FPFederico Pietrocola
Federico Pietrocola
SLS Lachkar
S Lachkar
DED P Enot
D P Enot
MNMireia Niso-Santano
Mireia Niso-Santano
José Manuel Bravo San PedroJosé Manuel Bravo San Pedro
José Manuel Bravo San Pedro
Guido KroemerGuido Kroemer
Guido Kroemer
Several natural compounds found in health-related food items can inhibit acetyltransferases as they induce autophagy. Here we show that this applies to anacardic acid, curcumin, garcinol and spermidine, all of which reduce the acetylation level of cultured human cells as they induce signs of increased autophagic flux (such as the formation of green fluorescent protein-microtubule-associated protein 1A/1B-light chain 3 (GFP-LC3) puncta and the depletion of sequestosome-1, p62/SQSTM1) coupled to the inhibition of the mammalian target of rapamycin complex 1 (mTORC1). We performed a screen to identify the acetyltransferases whose depletion would activate autophagy and simultaneously inhibit mTORC1. The knockdown of only two acetyltransferases (among 43 candidates) had such effects: EP300 (E1A-binding protein p300), which is a lysine acetyltranferase, and NAA20 (N(α)-acetyltransferase 20, also known as NAT5), which catalyzes the N-terminal acetylation of methionine residues. Subsequent studies validated the capacity of a pharmacological EP300 inhibitor, C646, to induce autophagy in both normal and enucleated cells (cytoplasts), underscoring the capacity of EP300 to repress autophagy by cytoplasmic (non-nuclear) effects. Notably, anacardic acid, curcumin, garcinol and spermidine all inhibited the acetyltransferase activity of recombinant EP300 protein in vitro. Altogether, these results support the idea that EP300 acts as an endogenous repressor of autophagy and that potent autophagy inducers including spermidine de facto act as EP300 inhibitors.

1 October 2013 in Seminars in Cancer Biology
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Journal Article
Closed access
FPFederico Pietrocola
Federico Pietrocola
VIValentina Izzo
Valentina Izzo
MNMireia Niso-Santano
Mireia Niso-Santano
EVErika Vacchelli
Erika Vacchelli
LGLorenzo Galluzzi
Lorenzo Galluzzi
Guido KroemerGuido Kroemer
Guido Kroemer