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Sofia C. Pérez Otero

Bio: Sofia C. Pérez Otero is an academic researcher from University of Puerto Rico, Río Piedras. The author has contributed to research in topics: Transferrin & Ribonucleotide reductase. The author has an hindex of 1, co-authored 2 publications receiving 21 citations.

Papers
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Journal ArticleDOI
TL;DR: Based on its chemical similarities with Fe, the biological coordination chemistry of Fe(III) and Ti(IV) is compared and it is hypothesized that Ti( IV) can bind to similar intracellular biomolecules and inhibit Fe bioavailability.

32 citations

Journal ArticleDOI
28 Jun 2021
TL;DR: In this paper, an intracellular iron chelator transmetalative approach was proposed to inhibit RNR using the titanium(IV) chemical transferrin mimetic (cTfm) compounds Ti(HBED) and Ti(Deferasirox)2.
Abstract: Efforts directed at curtailing the bioavailability of intracellular iron could lead to the development of broad-spectrum anticancer drugs given the metal's role in cancer proliferation and metastasis. Human ribonucleotide reductase (RNR), the key enzyme responsible for synthesizing the building blocks of DNA replication and repair, depends on Fe binding at its R2 subunit to activate the catalytic R1 subunit. This work explores an intracellular iron chelator transmetalative approach to inhibit RNR using the titanium(IV) chemical transferrin mimetic (cTfm) compounds Ti(HBED) and Ti(Deferasirox)2. Whole-cell EPR studies reveal that the compounds can effectively attenuate RNR activity though seemingly causing different changes to the labile iron pool that may account for differences in their potency against cells. Studies of Ti(IV) interactions with the adenosine nucleotide family at pH 7.4 reveal strong metal binding and extensive phosphate hydrolysis, which suggest the capacity of the metal to disturb the nucleotide substrate pool of the RNR enzyme. By decreasing intracellular Fe bioavailability and altering the nucleotide substrate pool, the Ti cTfm compounds could inhibit the activity of the R1 and R2 subunits of RNR. The compounds arrest the cell cycle in the S phase, indicating suppressed DNA replication, and induce apoptotic cell death. Cotreatment cell viability studies with cisplatin and Ti(Deferasirox)2 reveal a promising synergism between the compounds that is likely owed to their distinct but complementary effect on DNA replication.

5 citations


Cited by
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Journal ArticleDOI
30 Nov 2018
TL;DR: Efforts to improve the cellular delivery, efficacy, and tumor responsiveness of these chelators are presented including a transmetallation strategy for dual targeting of Cu and Fe.
Abstract: A very promising direction in the development of anticancer drugs is inhibiting the molecular pathways that keep cancer cells alive and able to metastasize. Copper and iron are two essential metals that play significant roles in the rapid proliferation of cancer cells and several chelators have been studied to suppress the bioavailability of these metals in the cells. This review discusses the major contributions that Cu and Fe play in the progression and spreading of cancer and evaluates select Cu and Fe chelators that demonstrate great promise as anticancer drugs. Efforts to improve the cellular delivery, efficacy, and tumor responsiveness of these chelators are also presented including a transmetallation strategy for dual targeting of Cu and Fe. To elucidate the effectiveness and specificity of Cu and Fe chelators for treating cancer, analytical tools are described for measuring Cu and Fe levels and for tracking the metals in cells, tissue, and the body.

63 citations

Journal ArticleDOI
TL;DR: Blood/serum titanium levels associated with well-functioning and malfunctioning prostheses are summarized, so that the prospects of using titanium measurements to gain insights into implant performance can be evaluated.

40 citations

Journal ArticleDOI
TL;DR: By closely examining the biological use of TiO2 and the influence of biomolecules on its stability and solubility, the reactivity of the material is reassessed in the presence and absence of UV energy.
Abstract: Titanium is one of the most abundant elements in the earth’s crust and while there are many examples of its bioactive properties and use by living organisms, there are few studies that have probed its biochemical reactivity in physiological environments. In the cosmetic industry, TiO2 nanoparticles are widely used. They are often incorporated in sunscreens as inorganic physical sun blockers, taking advantage of their semiconducting property, which facilitates absorbing ultraviolet (UV) radiation. Sunscreens are formulated to protect human skin from the redox activity of the TiO2 nanoparticles (NPs) and are mass-marketed as safe for people and the environment. By closely examining the biological use of TiO2 and the influence of biomolecules on its stability and solubility, we reassess the reactivity of the material in the presence and absence of UV energy. We also consider the alarming impact that TiO2 NP seepage into bodies of water can cause to the environment and aquatic life, and the effect that it can have on human skin and health, in general, especially if it penetrates into the human body and the bloodstream.

38 citations

Journal ArticleDOI
TL;DR: Lower level serum Co was positively associated with LBW and lower level serum Ti was negatively associated withLBW, especially gestational age >13 weeks, and both of them had non-linearity dose-relationships with LBw.

28 citations

Journal ArticleDOI
TL;DR: Prodigiosin, a natural pigment produced as a secondary metabolite by the non-photosynthetic bacterium Serratia marcescens, was tested as a sensitizer in dye-sensitized solar cells as mentioned in this paper.

23 citations