School of Food Science and Engineering, South China University of Technology, Guangzhou 510641, Guangdong, PR China.
School of Food Science and Engineering, South China University of Technology, Guangzhou 510641, Guangdong, PR China.
Biomed Pharmacother. 2021 Oct;142:112016. doi: 10.1016/j.biopha.2021.112016. Epub 2021 Aug 9.
The incidence and associated mortality of melanoma have increased significantly in recent years but treatment options are plagued with many undesirable side effects. Traditional Chinese herbal medicine polysaccharides are gaining increasing attention due to their potential role in the treatment of chronic diseases including tumors and the regulation of the immune system.
In this study, the potential effects of Ganoderma lucidum crude polysaccharides (GLCP) and Codonopsis pilosula crude polysaccharides (CPCP) on melanoma in C57 mice were explored. In addition, the inhibition and repolarization effect of digested Codonopsis pilosula polysaccharide (dCPP) on the proliferation of tumor-associated macrophages (TAMs) with M2-like phenotype induced by IL-4 were investigated.
The results showed that the various polysaccharides could significantly reduce tumor volume in melanoma mice. GLCP and GLCP + CPCP could further significantly reduce the number of CD68 macrophages in tumors and also prolong survival in melanoma mice to a certain extent. Significantly, dCPP could inhibit the proliferation of IL-4-induced M2-like TAMs, and significantly increase the mRNA expression levels of IL-1, IL-6, iNOS and TNF-a, thereby promoting the repolarization of M2-like TAMs to M1-like TAMs.
Overall, it could be deduced that GLCP, CPCP and dCPP hold great potential as safe therapeutic options for melanoma and an immune-modulator which may require further exploration.
近年来,黑色素瘤的发病率和相关死亡率显著上升,但治疗选择存在许多不良副作用。由于传统中草药多糖在治疗肿瘤等慢性病和调节免疫系统方面的潜在作用,它们越来越受到关注。
本研究探讨了灵芝粗多糖(GLCP)和党参粗多糖(CPCP)对 C57 小鼠黑色素瘤的潜在影响。此外,还研究了消化党参多糖(dCPP)对 IL-4 诱导的肿瘤相关巨噬细胞(TAMs)向 M2 样表型增殖的抑制和再极化作用。
结果表明,各种多糖均可显著降低黑色素瘤小鼠的肿瘤体积。GLCP 和 GLCP+CPCP 可进一步显著减少肿瘤中 CD68 巨噬细胞的数量,并在一定程度上延长黑色素瘤小鼠的生存时间。值得注意的是,dCPP 可抑制 IL-4 诱导的 M2 样 TAMs 的增殖,并显著增加 IL-1、IL-6、iNOS 和 TNF-a 的 mRNA 表达水平,从而促进 M2 样 TAMs 向 M1 样 TAMs 的再极化。
总之,可以推断 GLCP、CPCP 和 dCPP 作为黑色素瘤的安全治疗选择和免疫调节剂具有很大的潜力,这可能需要进一步探索。