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René Nieves-Alicea

Researcher at University of Texas MD Anderson Cancer Center

Publications -  16
Citations -  1012

René Nieves-Alicea is an academic researcher from University of Texas MD Anderson Cancer Center. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 13, co-authored 16 publications receiving 966 citations. Previous affiliations of René Nieves-Alicea include University of Texas Health Science Center at Houston & University of Puerto Rico, Medical Sciences Campus.

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Identification of thioaptamer ligand against E-selectin: potential application for inflamed vasculature targeting.

TL;DR: The discovery of a thioaptamer (ESTA-1) that binds to E-selectin with high affinity and specificity is substantiated, thereby highlighting the potential application of ESTA-1 for E- selectin targeted delivery.
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In vivo evaluation of safety of nanoporous silicon carriers following single and multiple dose intravenous administrations in mice.

TL;DR: Evidence of a safe intravenous administration of S1MPs as a drug delivery carrier is provided and pSi structures designed as a cargo for nanocarrier drug delivery to enable the loaded therapeutics and diagnostics to sequentially overcome the biological barriers in order to reach their target.
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Thioaptamer conjugated liposomes for tumor vasculature targeting.

TL;DR: This study has developed long circulating liposomes with the outer surface decorated with thioated oligonucleotide aptamer (thioaptamer) against E-selectin (ESTA) and evaluated the targeting efficacy and PK parameters, and opens the door to testing various combinations of thIOaptamer and nanocarriers that can be constructed to target multiple cancer types and tumor components for delivery of both therapeutics and imaging agents.
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Programmed cell death 4 inhibits breast cancer cell invasion by increasing tissue inhibitor of metalloproteinases-2 expression.

TL;DR: The novel findings that suppression of PDCD4 expression is vital for the invasive activity of COX-2 mediated by PGE2 and IL-8, and that PD CD4 increases TIMP-2 expression to inhibit breast cancer cell invasion are reported.