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Stefania D'Atri

Researcher at University of Rome Tor Vergata

Publications -  98
Citations -  5581

Stefania D'Atri is an academic researcher from University of Rome Tor Vergata. The author has contributed to research in topics: Melanoma & Cytotoxic T cell. The author has an hindex of 31, co-authored 93 publications receiving 4694 citations.

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Genomic Classification of Cutaneous Melanoma

Rehan Akbani, +351 more
- 18 Jun 2015 - 
TL;DR: This clinicopathological and multi-dimensional analysis suggests that the prognosis of melanoma patients with regional metastases is influenced by tumor stroma immunobiology, offering insights to further personalize therapeutic decision-making.
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Involvement of the mismatch repair system in temozolomide-induced apoptosis

TL;DR: The existence of a link between a functional mismatch repair system and the trigger of apoptosis in cells exposed to clinically relevant concentrations of temozolomide is demonstrated and the results suggest that p53 induction in response to O6-guanine methylation involves the mismatchrepair system.
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Downregulation of 14-3-3σ Prevents Clonal Evolution and Leads to Immortalization of Primary Human Keratinocytes

TL;DR: Downregulation of 14-3-3σ, which is specifically expressed in human stratified epithelia, prevents keratinocyte clonal evolution, thereby forcing keratinocytes into the stem cell compartment, and suggest that inhibition of a single endogenous gene product fosters immortalization of primary human epithelial cells without the need of exogenous oncogenes and/or oncoviruses.
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DNA damage induced by temozolomide signals to both ATM and ATR: role of the mismatch repair system.

TL;DR: It is demonstrated that TMZ treatment activates ATM- and ATR-dependent signaling pathways and that this process is absolutely dependent on functional MMR only at low drug concentrations.
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Human Melanoma Cells Secrete and Respond to Placenta Growth Factor and Vascular Endothelial Growth Factor

TL;DR: Both primary and metastatic melanoma cells were found to express the mRNAs encoding for vascular endothelial growth factor and placenta growth factor receptors, and exposure of melanomas cells to these cytokines resulted in a specific proliferative response, supporting the hypothesis of a role of these angiogenic factors in melanoma growth.