Defining a molecular subclass of treatment resistant prostate cancer.

2015 ◽  
Vol 33 (15_suppl) ◽  
pp. 5004-5004 ◽  
Author(s):  
Himisha Beltran ◽  
Davide Prandi ◽  
Juan Miguel Mosquera ◽  
Eugenia Giannopoulou ◽  
Loredana Puca ◽  
...  
2015 ◽  
Author(s):  
Himisha Beltran ◽  
Davide Prandi ◽  
Juan Miguel Mosquera ◽  
Eugenia Giannopoulou ◽  
Loredana Puca ◽  
...  

Cancers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 692
Author(s):  
Roosa Kaarijärvi ◽  
Heidi Kaljunen ◽  
Kirsi Ketola

Neuroendocrine plasticity and treatment-induced neuroendocrine phenotypes have recently been proposed as important resistance mechanisms underlying prostate cancer progression. Treatment-induced neuroendocrine prostate cancer (t-NEPC) is highly aggressive subtype of castration-resistant prostate cancer which develops for one fifth of patients under prolonged androgen deprivation. In recent years, understanding of molecular features and phenotypic changes in neuroendocrine plasticity has been grown. However, there are still fundamental questions to be answered in this emerging research field, for example, why and how do the prostate cancer treatment-resistant cells acquire neuron-like phenotype. The advantages of the phenotypic change and the role of tumor microenvironment in controlling cellular plasticity and in the emergence of treatment-resistant aggressive forms of prostate cancer is mostly unknown. Here, we discuss the molecular and functional links between neurodevelopmental processes and treatment-induced neuroendocrine plasticity in prostate cancer progression and treatment resistance. We provide an overview of the emergence of neurite-like cells in neuroendocrine prostate cancer cells and whether the reported t-NEPC pathways and proteins relate to neurodevelopmental processes like neurogenesis and axonogenesis during the development of treatment resistance. We also discuss emerging novel therapeutic targets modulating neuroendocrine plasticity.


Author(s):  
Alastair Davies ◽  
Shaghayegh Nouruzi ◽  
Dwaipayan Ganguli ◽  
Takeshi Namekawa ◽  
Daksh Thaper ◽  
...  

The Prostate ◽  
2019 ◽  
Vol 79 (16) ◽  
pp. 1837-1851 ◽  
Author(s):  
Jin‐Yih Low ◽  
Paul Sirajuddin ◽  
Michael Moubarek ◽  
Shreya Agarwal ◽  
Apurv Rege ◽  
...  

2018 ◽  
Author(s):  
Shayna Elizabeth Thomas-Jardin ◽  
Mohammed Kanchwala ◽  
Joan Jacob ◽  
Rachel Meade ◽  
Nagham Gahnim ◽  
...  

2011 ◽  
Vol 74 (8) ◽  
pp. 1731-1736 ◽  
Author(s):  
Samy A. F. Morad ◽  
Claudia Schmidt ◽  
Berthold Büchele ◽  
Bernd Schneider ◽  
Michael Wenzler ◽  
...  

2020 ◽  
Vol 13 ◽  
Author(s):  
Selin Soyluoglu ◽  
Gulay Durmus-Altun

Background: Theranostic is a new field of medicine that combines diagnosis and patient-specific targeted treatment. In the theranostic approach, it is aimed to detect diseased cells by using targeted molecules using disease-specific biological pathways and then destroy them by cellular irradiation without damaging other tissues. Diagnostic tests guide the use of specific therapeutic agents by demonstrating the presence of the receptor/molecule on the target tissue. Because the therapeutic agent is administered to patients who have a positive diagnostic test, the efficacy of treatment in these patients is largely guaranteed. As therapeutic efficacy can be predicted by therapeutic agents, it is also possible to monitor the response to treatment. Many diagnostic and therapeutic procedures in nuclear medicine are classified as theranostic. 131I treatment and scintigraphy is the best example of theranostic application. Likewise, 177Lu / 90Y octreotate for neuroendocrine tumors, 177Lu PSMA for metastatic or treatment-resistant prostate cancer, 90Y SIRT for metastatic liver cancer, and 223Ra for bone metastasis of prostate cancer are widely used. Also nanoparticles are one of the most rapidly developing subjects of theranostics. Diagnostic and therapeutic agents that show fluorescent, ultrasonic, magnetic, radioactive, contrast, pharmacological drug or antibody properties are loaded into the nanoparticle to provide theranostatic use. Method: This article will review general aspects of preclinical models for theranostic research, and present examples from the literature. Conclusion: To achieve successful results in rapidly accelerating personalized treatment research of today, the first step is to conduct appropriate preclinical studies.


2016 ◽  
Vol 2 (5) ◽  
pp. 469-471 ◽  
Author(s):  
Rahul Aggarwal ◽  
Tomasz M. Beer ◽  
Martin Gleave ◽  
Joshua M. Stuart ◽  
Matthew Rettig ◽  
...  

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