In vitro evaluation of the new radiotracer 99mTc-HYNIC-PSMA for prostate cancer diagnosis
Joint Event on International Conference on Plastic and Cosmetic Surgery & International Conference on Biomarkers
March 11-12, 2019 | London, UK
Monika Orzelowska, Michal Maurin and Piotr Garnuszek
National Centre for Nuclear Research Radioisotope Centre POLATOM, Poland
Posters & Accepted Abstracts : Case Rep Surg Invasive Proced
Abstract:
Introduction: Prostate cancer is the second commonly occurring
malignance in men. The selection of an effective therapy form
depends on the proper assessment of the disease progression.
The prostate-specific membrane antigen (PSMA) is becoming
increasingly recognized as a viable target for imaging and therapy
of prostate and other types of cancer.
As it is important to fully characterize the properties of
radiolabelled compounds before in vivo studies, the aim
of this work was to evaluate the in vitro biological activity
of new developed PSMA inhibitor - 99mTc-HYNIC-PSMApotential
tracer for SPECT diagnosis of prostate cancer.
Method: Saturation binding assay was performed to determine
specificity of binding, dissociation constant (Kd) and maximal
concentration of receptors on the cell surface (Bmax). HYNICPSMA
inhibitor was labelled with 99mTc. The binding of 99mTc-
HYNIC-PSMA was evaluated by carrying out the studies using
the cell membranes isolated from LNCaP cells. The non-specific
binding was determined using membranes isolated from PC3
cells known not to express PSMA. IC50 values of the tested
compounds were determined by competitive binding assay
on LNCaP cell membranes using 131I-MIP1095 radioligand
with known high affinity to PSMA (IC50=0.3). As a reference
substance, PSMA11 was used.
Results: 99mTc-PSMA-T4 showed high specific affinity to
PSMA, which represented 99% of total binding. The Kd value
determined from the specific binding of the tested radioligand
was 5.47 nM and the Bmax was 9533 pmol/mg. The IC50 value
of HYNIC-PSMA was assessed at the level of 79.5 and it was 10
times lower than value obtained for PSMA11.
Conclusion: High specific binding of 99mTc-HYNIC-PSMA to
the PSMA suggests its huge potential for prostate cancer
diagnosis. Comparison of the affinities of 99mTc-HYNIC-PSMA
and 68Ga-PSMA11 points out that despite SPECT technique
has a lower spatial resolution than PET, 99mTc-HYNIC-PSMA
can be a useful alternative in diagnosis and staging of prostate
cancer.
Biography:
Monika OrzeĊowska graduated in Biotechnology from the Faculty of Biology and Biotechnology in Maria-Curie Sklodowska University in Lublin, Poland. She obtained a master’s degree in 2014. In August 2015, she started work in R&D Department at National Centre for Nuclear Research, Radioisotope Centre POLATOM.
E-mail: Monika.Orzelowska@polatom.pl
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