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Saveria Aquila

Researcher at University of Calabria

Publications -  93
Citations -  9125

Saveria Aquila is an academic researcher from University of Calabria. The author has contributed to research in topics: Sperm & Receptor. The author has an hindex of 36, co-authored 90 publications receiving 8213 citations.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Metabolic reprogramming of cancer-associated fibroblasts by TGF-β drives tumor growth: Connecting TGF-β signaling with “Warburg-like” cancer metabolism and L-lactate production

TL;DR: Ligand-dependent or cell-autonomous activation of the TGF-β pathway in stromal cells induces their metabolic reprogramming, with increased oxidative stress, autophagy/mitophagy and glycolysis, and downregulation of Cav-1, and establishes a clear causative link between the tumor-promoting effects of T GF-β signaling and the metabolicReprogramming of the tumor microenvironment.
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Estrogen Receptor (ER)α and ERβ Are Both Expressed in Human Ejaculated Spermatozoa: Evidence of Their Direct Interaction with Phosphatidylinositol-3-OH Kinase/Akt Pathway

TL;DR: The concomitant expression of ER beta and ER alpha in human ejaculated spermatozoa is demonstrated and a different interaction of the two ERs with the PI3K/Akt pathway is provided, for the first time, because ER alpha interacts with the p55 regulatory subunit ofPI3K, whereas ER beta interacts with Akt1.
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Estrogen receptor alpha binds to peroxisome proliferator-activated receptor response element and negatively interferes with peroxisome proliferator-activated receptor gamma signaling in breast cancer cells

TL;DR: The data show for the first time that ERα binds to PPAR response element and represses its transactivation, and this crosstalk between ERα and PPARγ pathways in breast cancer cells could be taken into account in setting new pharmacologic strategies for breast cancer disease.
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G protein-coupled receptor 30 expression is up-regulated by EGF and TGF alpha in estrogen receptor alpha-positive cancer cells

TL;DR: The data may suggest that ligand-activated EGFR could contribute to the failure of tamoxifen therapy also by up-regulating GPR30, which in turn could facilitates the action of estrogen.