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Open AccessJournal ArticleDOI

Towards Personalized Treatment of Prostate Cancer: PSMA I&T, a Promising Prostate-Specific Membrane Antigen-Targeted Theranostic Agent.

TLDR
The preclinical application of PSMA I&T, a DOTAGA-chelated urea-based PSMA inhibitor, for SPECT/CT imaging and radionuclide therapy of prostate cancer is presented and indicates that PSMA-specific uptake in kidneys can be successfully tackled using blocking agents such as 2-PMPA.
Abstract
Prostate-specific membrane antigen (PSMA) is a well-established target for nuclear imaging and therapy of prostate cancer (PCa). Radiolabeled small-molecule PSMA inhibitors are excellent candidates for PCa theranostics-they rapidly and efficiently localize in tumor lesions. However, high tracer uptake in kidneys and salivary glands are major concerns for therapeutic applications. Here, we present the preclinical application of PSMA IT however, high renal and spleen uptake in control mice (no 2-PMPA) interfered with visualization of metastases in the vicinity of those organs. Coadministration of 2-PMPA increased the tumor-to-kidney absorbed dose ratio during (177)Lu-PSMA I&T radionuclide therapy. Hence, at equivalent absorbed dose to the tumor (36 Gy), coinjection of 2-PMPA decreased absorbed dose to the kidneys from 30 Gy to 12 Gy. Mice injected with (177)Lu-PSMA I&T only, showed signs of nephrotoxicity at 3 months after therapy, whereas mice injected with (177)Lu-PSMA I&T + 2-PMPA did not. These data indicate that PSMA I&T is a promising theranostic tool for PCa. PSMA-specific uptake in kidneys can be successfully tackled using blocking agents such as 2-PMPA.

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Journal ArticleDOI

Radioactive Transition Metals for Imaging and Therapy.

TL;DR: This Review provides an overview of some of the ways that new technologies, primarily related to radionuclide production, have provided solutions to these problems and several historical examples of the limitations of earlier metalloradiopharmaceuticals.
Journal ArticleDOI

131I-labeled Anti-HER2 Camelid sdAb as a Theranostic Tool in Cancer Treatment

TL;DR: The generation of a 131I-labeled sdAb as a theranostic drug to treat HER2-overexpressing cancer and demonstrate the theranostics potential of [131I]SGMIB-2Rs15d could impact therapy outcome on HER2+ breast cancer patients.
Journal ArticleDOI

Gut Microbiota-Mediated Personalized Treatment of Hyperlipidemia Using Berberine.

TL;DR: It is shown here that feeding hamsters with high fat diet (HFD) caused an increase in blood lipids and NR activity in the intestine and the fecal NR activity might serve as a biomarker in the personalized treatment of hyperlipidemia using BBR.
Journal ArticleDOI

Enhancing Treatment Efficacy of 177Lu-PSMA-617 with the Conjugation of an Albumin-Binding Motif: Preclinical Dosimetry and Endoradiotherapy Studies.

TL;DR: A novel albumin-binder-conjugated 177Lu-PSMA-617 derivative with an extended blood retention time to maximize the radiation dose delivered to prostate tumors expressing prostate-specific membrane antigen (PSMA) warrants further investigation for endoradiotherapy of prostate cancer.
References
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Journal ArticleDOI

Cancer treatment and survivorship statistics, 2012

TL;DR: Common cancer treatments, survival rates, and posttreatment concerns are summarized and the new National Cancer Survivorship Resource Center is introduced, which has engaged more than 100 volunteer survivorship experts nationwide to develop tools for cancer survivors, caregivers, health care professionals, advocates, and policy makers.
Journal ArticleDOI

EAU Guidelines on Prostate Cancer. Part 1: Screening, Diagnosis, and Local Treatment with Curative Intent—Update 2013

TL;DR: Current evidence is insufficient to warrant widespread population-based screening by prostate-specific antigen (PSA) for PCa, and watchful waiting is a treatment alternative to androgen-deprivation therapy (ADT), with equivalent oncologic efficacy.
Journal Article

Prostate-specific membrane antigen expression in normal and malignant human tissues.

TL;DR: The decrease in PSMA immunoreactivity noted in advanced prostate cancer suggests that expression of this molecule may be linked to the degree of tumor differentiation and the neoexpression of PSMA in endothelial cells of capillary beds in certain tumors may be related to tumor angiogenesis and suggests a potential mechanism for specific targeting of tumor neovasculature.
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