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1.
Clin. transl. oncol. (Print) ; 23(2): 197-204, feb. 2021. ilus
Article in English | IBECS | ID: ibc-220603

ABSTRACT

In modern medicine, natural products have aided humans against their battles with cancer. Among these products, microorganisms, medicinal herbs and marine organisms are considered to be of great benefit. In recent decades, more than 30 fungal immunity proteins have been identified and proved to be extractable from a wide range of fungi, including mushrooms. Although chemotherapy is used to overcome cancer cells, the side effects of this method are of great concern in clinical practice. Fungal products and their derivatives constitute more than 50% of the clinical drugs currently being used globally. Approximately 60% of the clinically approved drugs for cancer treatment have natural roots. Anti-tumor immunotherapy is prospective with a rapidly growing market worldwide due to its high efficiency, immunity, and profit. Polysaccharide extracts from natural sources are being used in clinical and therapeutic trials on cancer patients. This review aims to present the latest findings in cancer treatment through isolated and extraction of fungal derivatives and other natural biomaterials (AU)


Subject(s)
Humans , Antineoplastic Agents/therapeutic use , Biological Products/therapeutic use , Fungi/chemistry , Neoplasms/drug therapy , Agaricales/chemistry , Anti-Inflammatory Agents/therapeutic use , Basidiomycota/chemistry , Fungal Polysaccharides/therapeutic use , Fungal Proteins/therapeutic use , Fungi/metabolism , Nanoparticles/therapeutic use , Neoplasms/immunology
2.
Clin Transl Oncol ; 23(2): 197-204, 2021 Feb.
Article in English | MEDLINE | ID: mdl-32557335

ABSTRACT

In modern medicine, natural products have aided humans against their battles with cancer. Among these products, microorganisms, medicinal herbs and marine organisms are considered to be of great benefit. In recent decades, more than 30 fungal immunity proteins have been identified and proved to be extractable from a wide range of fungi, including mushrooms. Although chemotherapy is used to overcome cancer cells, the side effects of this method are of great concern in clinical practice. Fungal products and their derivatives constitute more than 50% of the clinical drugs currently being used globally. Approximately 60% of the clinically approved drugs for cancer treatment have natural roots. Anti-tumor immunotherapy is prospective with a rapidly growing market worldwide due to its high efficiency, immunity, and profit. Polysaccharide extracts from natural sources are being used in clinical and therapeutic trials on cancer patients. This review aims to present the latest findings in cancer treatment through isolated and extraction of fungal derivatives and other natural biomaterials.


Subject(s)
Antineoplastic Agents/therapeutic use , Biological Products/therapeutic use , Fungi/chemistry , Neoplasms/drug therapy , Agaricales/chemistry , Anti-Inflammatory Agents/therapeutic use , Basidiomycota/chemistry , Fungal Polysaccharides/therapeutic use , Fungal Proteins/therapeutic use , Fungi/metabolism , Humans , Nanoparticles/therapeutic use , Neoplasms/immunology
3.
Curr Med Mycol ; 2(2): 16-19, 2016 Jun.
Article in English | MEDLINE | ID: mdl-28681015

ABSTRACT

BACKGROUND AND PURPOSE: MicroRNAs are small non-coding RNAs with 19-24 nucleotides in length. Up- or down-regulation of many miRNAs has been shown by stimulation of Toll-like receptors (TLRs) in the innate immune system. Up-regulation of miR-146a has been reported by both TLR and heat-killed Candida albicans. In this study, we aimed to evaluate the expression of miR-146a in cultured monocyte-derived macrophages (MDMs) infected by Candida glabrata at 12, 24, and 48 hours. MATERIALS AND METHODS: miR-146a expression was evaluated by qRT-real time polymerase chain reaction (PCR) at three time points in C. glabrata-infected MDMs. The data was analyzed using repeated measures ANOVA. RESULTS: miR-146a expression was down-regulated in infected MDMs compared to the control group (P<0.018). The expression of miR-146a was at its highest level at 48 h, as compared to 12 and 24 h (P<0.018) .The differences between the experimental group compared to the control group were statistically significant (P<0.018). CONCLUSION: These results suggest that miR-146a can be involved in regulating macrophage function following TLR stimulation in C.glabrata-infected MDMs.

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