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Farshad Mirzavi

Researcher at Mashhad University of Medical Sciences

Publications -  27
Citations -  113

Farshad Mirzavi is an academic researcher from Mashhad University of Medical Sciences. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 3, co-authored 5 publications receiving 15 citations.

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A review on liposome-based therapeutic approaches against malignant melanoma.

TL;DR: An overview of liposome-based targeted drug delivery methods for melanoma is presented in this article, where the new insights regarding the efficacy and clinical significance of combinatorial treatment with liposomal formulations with immunotherapy and conventional therapies in melanoma patients are discussed.
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SP/NK1R system regulate carcinogenesis in prostate cancer: Shedding light on the antitumoral function of aprepitant.

TL;DR: In this article , the authors found that SP acting via neurokinin-1-receptor (NK1R) promotes tumorigenicity in many human malignant tumors, but its pro-tumorigenic functions and the therapeutic effects of its inhibition in prostate cancer remain unclear.
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The therapeutic potential of targeting CD73 and CD73-derived adenosine in melanoma.

TL;DR: This paper aims to comprehensively review the therapeutic potential of CD73 ectonucleotidase targeting in melanoma, and depicts the metabolism and signaling ofCD73-derived adenosine along with its progressive role in development of melanoma.
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Enhanced antitumor immune response in melanoma tumor model by anti-PD-1 small interference RNA encapsulated in nanoliposomes

TL;DR: Wang et al. as discussed by the authors used a liposomal formulation as a siRNA carrier to silence PD-1 expression in T cells and investigate it's in vivo antitumor efficacy.
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Tumor-Inhibitory Effects of Zerumbone Against HT-29 Human Colorectal Cancer Cells

TL;DR: Zerumbone significantly inhibited the migration of HT-29 cells and decreased MMP-2/-9 mRNA expression and activity and could be developed as a promising natural agent for future CRC therapy.