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Francesca Spinella

Researcher at University of Naples Federico II

Publications -  75
Citations -  4332

Francesca Spinella is an academic researcher from University of Naples Federico II. The author has contributed to research in topics: Angiogenesis & Ovarian carcinoma. The author has an hindex of 36, co-authored 75 publications receiving 3805 citations. Previous affiliations of Francesca Spinella include National Research Council.

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Endothelin 1 in cancer: biological implications and therapeutic opportunities.

TL;DR: The advances in the understanding of the diverse biological roles of ET1 are discussed and the latest preclinical and clinical progress that has been made using small-molecule antagonists ofET1 receptors that inhibit ET1-driven signalling are described.
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Correlation between aneuploidy, standard morphology evaluation and morphokinetic development in 1730 biopsied blastocysts: a consecutive case series study

TL;DR: Correlations were observed, in that euploid human blastocysts showed a higher percentage with top quality inner cell mass (ICM) and trophectoderm (TE), higher expansion grades and shorter time to start of blastulation, expansion and hatching, compared to aneuploid ones.
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Endothelin-1 Induces Vascular Endothelial Growth Factor by Increasing Hypoxia-inducible Factor-1α in Ovarian Carcinoma Cells *

TL;DR: The results suggest that new therapeutic strategies using specific ETAR antagonists could provide an additional approach to the treatment of ovarian carcinoma by inhibiting neovascularization as well as tumor cell growth, and provide a mechanism whereby ET-1 acting selectively through ETAR can interact with the HIF-1α-dependent machinery of angiogenesis.
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Acquisition of chemoresistance and EMT phenotype is linked with activation of the endothelin A receptor pathway in ovarian carcinoma cells

TL;DR: The data provide the first evidence that blockade of ETAR-driven EMT can overcome chemoresistance and inhibit tumor progression, improving the outcome of EOC patients' treatment.
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Endothelin-1 promotes epithelial-to-mesenchymal transition in human ovarian cancer cells

TL;DR: It is shown that the ET-1/ET(A)R autocrine pathway drives epithelial-to-mesenchymal transition (EMT) in ovarian tumor cells by inducing a fibroblastoid and invasive phenotype, down-regulation of E-cadherin, increased levels of beta-catenin, Snail, and other mesenchymic markers, and suppression of E/E/R promoter activity.