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Molecular targets for anticancer therapies in companion animals and humans: what can we learn from each other?

作者信息

Beltrán Hernández Irati, Kromhout Jannes Z, Teske Erik, Hennink Wim E, van Nimwegen Sebastiaan A, Oliveira Sabrina

机构信息

Pharmaceutics, Department of Pharmaceutical Sciences, Faculty of Science, Utrecht University, 3584 CG Utrecht, the Netherlands.

Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, 3584 CH Utrecht, the Netherlands.

出版信息

Theranostics. 2021 Feb 6;11(8):3882-3897. doi: 10.7150/thno.55760. eCollection 2021.


DOI:10.7150/thno.55760
PMID:33664868
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7914358/
Abstract

Despite clinical successes in the treatment of some early stage cancers, it is undeniable that novel and innovative approaches are needed to aid in the fight against cancer. Targeted therapies offer the desirable feature of tumor specificity while sparing healthy tissues, thereby minimizing side effects. However, the success rate of translation of these therapies from the preclinical setting to the clinic is dramatically low, highlighting an important point of necessary improvement in the drug development process in the oncology field. The practice of a comparative oncology approach can address some of the current issues, by introducing companion animals with spontaneous tumors in the linear drug development programs. In this way, animals from the veterinary clinic get access to novel/innovative therapies, otherwise inaccessible, while generating robust data to aid therapy refinement and increase translational success. In this review, we present an overview of targetable membrane proteins expressed in the most well-characterized canine and feline solid cancers, greatly resembling the counterpart human malignancies. We identified particular areas in which a closer collaboration between the human and veterinary clinic would benefit both human and veterinary patients. Considerations and challenges to implement comparative oncology in the development of anticancer targeted therapies are also discussed.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b705/7914358/0d81f8b3ff6a/thnov11p3882g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b705/7914358/33c01aa64c09/thnov11p3882g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b705/7914358/0d81f8b3ff6a/thnov11p3882g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b705/7914358/33c01aa64c09/thnov11p3882g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b705/7914358/0d81f8b3ff6a/thnov11p3882g002.jpg

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本文引用的文献

[1]
Molecular homology between canine spontaneous oral squamous cell carcinomas and human head-and-neck squamous cell carcinomas reveals disease drivers and therapeutic vulnerabilities.

Neoplasia. 2020-12

[2]
Naturally-Occurring Canine Mammary Tumors as a Translational Model for Human Breast Cancer.

Front Oncol. 2020-4-28

[3]
Differential stromal reprogramming in benign and malignant naturally occurring canine mammary tumours identifies disease-modulating stromal components.

Sci Rep. 2020-3-26

[4]
Exploiting the folate receptor α in oncology.

Nat Rev Clin Oncol. 2020-3-9

[5]
Naturally-Occurring Invasive Urothelial Carcinoma in Dogs, a Unique Model to Drive Advances in Managing Muscle Invasive Bladder Cancer in Humans.

Front Oncol. 2020-1-21

[6]
Diverse roles of epidermal growth factors receptors in oral and cutaneous canine melanomas.

BMC Vet Res. 2020-1-29

[7]
Prospective clinical trial of masitinib mesylate treatment for advanced stage III and IV canine malignant melanoma.

J Small Anim Pract. 2020-3

[8]
In vitro and in vivo effects of toceranib phosphate on canine osteosarcoma cell lines and xenograft orthotopic models.

Vet Comp Oncol. 2019-12-15

[9]
Molecular Targeting Therapy against EGFR Family in Breast Cancer: Progress and Future Potentials.

Cancers (Basel). 2019-11-20

[10]
A novel MCT1 and MCT4 dual inhibitor reduces mitochondrial metabolism and inhibits tumour growth of feline oral squamous cell carcinoma.

Vet Comp Oncol. 2020-9

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