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Delia Mezzanzanica

Researcher at University of Milan

Publications -  115
Citations -  4743

Delia Mezzanzanica is an academic researcher from University of Milan. The author has contributed to research in topics: Monoclonal antibody & Antigen. The author has an hindex of 38, co-authored 109 publications receiving 4363 citations. Previous affiliations of Delia Mezzanzanica include National Institutes of Health.

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Characterization of human ovarian carcinoma‐associated antigens defined by novel monoclonal antibodies with tumor‐restricted specificity

TL;DR: Three new monoclonal antibodies (MAbs) were raised against human ovarian carcinoma, and the properties of these antibodies, their restricted ovarian tumor specificities and relative high affinity constants suggest that they could represent promising tools for in vivo applications.
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Alterations of Choline Phospholipid Metabolism in Ovarian Tumor Progression

TL;DR: Evidence of abnormal phosphatidylcholine metabolism might have implications in EOC biology and might provide an avenue to the development of noninvasive clinical tools for EOC diagnosis and treatment follow-up.
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Activation of Phosphatidylcholine Cycle Enzymes in Human Epithelial Ovarian Cancer Cells

TL;DR: Overall, it was shown that the elevated PCho pool detected in EOC cells primarily resulted from upregulation/activation of ChoK and PC-plc involved in PC biosynthesis and degradation, respectively.
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Cellular FLICE-inhibitory protein (c-FLIP) signalling: a key regulator of receptor-mediated apoptosis in physiologic context and in cancer.

TL;DR: The role of c-FLIP(L) as anti-apoptotic pro-survival factor in tumors and the potential utility of this molecule as a possible alternative therapeutic target are discussed.
Journal Article

The apoptosis inhibitor protein survivin induces tumor-specific CD8+ and CD4+ T cells in colorectal cancer patients.

TL;DR: It is shown that the inhibitor of apoptosis protein, survivin, is immunogenic in colorectal cancer patients, and it is found that survivin elicited CD8(+) T cell-mediated responses in peripheral blood or in tumor-associated lymphocytes from patients at different disease stage.