CHAPTER 12. Challenges and Chances in the Preclinical to Clinical Translation of Anticancer Metallodrugs

Author(s):  
Isabella Pötsch ◽  
Dina Baier ◽  
Bernhard K. Keppler ◽  
Walter Berger
2009 ◽  
Vol 9 (2) ◽  
pp. 83-90 ◽  
Author(s):  
Frank Jacobs ◽  
Yingmei Feng ◽  
Eline Craeyveld ◽  
Joke Lievens ◽  
Jan Snoeys ◽  
...  

MedChemComm ◽  
2019 ◽  
Vol 10 (12) ◽  
pp. 2111-2117 ◽  
Author(s):  
Kusum Vats ◽  
Kanhaiyalal Agrawal ◽  
Rohit Sharma ◽  
Haladhar Dev Sarma ◽  
Drishty Satpati ◽  
...  

This study explores the feasibility of radiolabeling the HBED-CC-PSMA (PSMA-11) ligand with Tc-99m for SPECT imaging of prostate cancer patients.


2018 ◽  
Vol 5 ◽  
Author(s):  
Cameron Keighron ◽  
Caomhán J. Lyons ◽  
Michael Creane ◽  
Timothy O'Brien ◽  
Aaron Liew

2021 ◽  
Vol 5 (2) ◽  
pp. 021503
Author(s):  
Muhammad Anwaar Nazeer ◽  
Ismail Can Karaoglu ◽  
Onur Ozer ◽  
Cem Albayrak ◽  
Seda Kizilel

2021 ◽  
Vol 22 ◽  
pp. 100264
Author(s):  
Qian Chen ◽  
Wei Qin ◽  
Weizhi Qi ◽  
Lei Xi

Neurosurgery ◽  
2020 ◽  
Author(s):  
Ben Jiahe Gu ◽  
David K Kung ◽  
Han-Chiao Isaac Chen

Abstract Cell therapy has been widely recognized as a promising strategy to enhance recovery in stroke survivors. However, despite an abundance of encouraging preclinical data, successful clinical translation remains elusive. As the field continues to advance, it is important to reexamine prior clinical trials in the context of their intended mechanisms, as this can inform future preclinical and translational efforts. In the present work, we review the major clinical trials of cell therapy for stroke and highlight a mechanistic shift between the earliest studies, which aimed to replace dead and damaged neurons, and later ones that focused on exploiting the various neuromodulatory effects afforded by stem cells. We discuss why both mechanisms are worth pursuing and emphasize the means through which cell replacement can still be achieved.


Marine Drugs ◽  
2021 ◽  
Vol 19 (4) ◽  
pp. 196
Author(s):  
Muhammad Bilal ◽  
Leonardo Vieira Nunes ◽  
Marco Thúlio Saviatto Duarte ◽  
Luiz Fernando Romanholo Ferreira ◽  
Renato Nery Soriano ◽  
...  

Naturally occurring biological entities with extractable and tunable structural and functional characteristics, along with therapeutic attributes, are of supreme interest for strengthening the twenty-first-century biomedical settings. Irrespective of ongoing technological and clinical advancement, traditional medicinal practices to address and manage inflammatory bowel disease (IBD) are inefficient and the effect of the administered therapeutic cues is limited. The reasonable immune response or invasion should also be circumvented for successful clinical translation of engineered cues as highly efficient and robust bioactive entities. In this context, research is underway worldwide, and researchers have redirected or regained their interests in valorizing the naturally occurring biological entities/resources, for example, algal biome so-called “treasure of untouched or underexploited sources”. Algal biome from the marine environment is an immense source of excellence that has also been demonstrated as a source of bioactive compounds with unique chemical, structural, and functional features. Moreover, the molecular modeling and synthesis of new drugs based on marine-derived therapeutic and biological cues can show greater efficacy and specificity for the therapeutics. Herein, an effort has been made to cover the existing literature gap on the exploitation of naturally occurring biological entities/resources to address and efficiently manage IBD. Following a brief background study, a focus was given to design characteristics, performance evaluation of engineered cues, and point-of-care IBD therapeutics of diverse bioactive compounds from the algal biome. Noteworthy potentialities of marine-derived biologically active compounds have also been spotlighted to underlying the impact role of bio-active elements with the related pathways. The current review is also focused on the applied standpoint and clinical translation of marine-derived bioactive compounds. Furthermore, a detailed overview of clinical applications and future perspectives are also given in this review.


2021 ◽  
Vol 12 ◽  
pp. 204173142110190
Author(s):  
Jung-Hwan Lee ◽  
Ji-Young Yoon ◽  
Jun Hee Lee ◽  
Hae-Hyoung Lee ◽  
Jonathan C Knowles ◽  
...  

Extracellular vesicles (EVs), including exosomes, carry the genetic packages of RNA, DNA, and proteins and are heavily involved in cell-cell communications and intracellular signalings. Therefore, EVs are spotlighted as therapeutic mediators for the treatment of injured and dysfunctional tissues as well as biomarkers for the detection of disease status and progress. Several key issues in EVs, including payload content and bioactivity, targeting and bio-imaging ability, and mass-production, need to be improved to enable effective therapeutics and clinical translation. For this, significant efforts have been made recently, including genetic modification, biomolecular and chemical treatment, application of physical/mechanical cues, and 3D cultures. Here we communicate those recent technological advances made mainly in the biogenesis process of EVs or at post-collection stages, which ultimately aimed to improve the therapeutic efficacy in tissue healing and disease curing and the possibility of clinical translation. This communication will help tissue engineers and biomaterial scientists design and produce EVs optimally for tissue regenerative therapeutics.


2021 ◽  
Vol 446 ◽  
pp. 214129
Author(s):  
Enrique Ortega ◽  
Gloria Vigueras ◽  
Francisco José Ballester ◽  
José Ruiz

Talanta ◽  
2021 ◽  
Vol 225 ◽  
pp. 122002
Author(s):  
Leila Syedmoradi ◽  
Michael L. Norton ◽  
Kobra Omidfar

Sign in / Sign up

Export Citation Format

Share Document