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| 學 曆:博士研究生
職 稱:講師 電子郵箱:mmwang@dgut.edu.cn 研究領域:1.生物活性材料對緻病蛋白的穩态調控 2.天然産物抗腫瘤活性及其機制研究
3.斑馬魚胚胎發育及藥物毒理研究
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一、教育、工作經曆:
2023年3與月-至今,太阳成集团tyc234cc,講師
2018年9月-2022年12月,華南理工大學醫學院,博士
2015年9月-2018年6月,西南大學藥學院,碩士
2011年9月-2015年6月,河南中醫藥大學藥學院,學士
二、研究領域:
主要從事研究領域包括:探讨生物活性材料對突變p53、β澱粉樣等緻病蛋白調控的機制;從中藥中分離的小分子以及蛋白大分子活性成分抗腫瘤機制研究;以斑馬魚為模式生物進行藥物篩選、毒性發現以及安全性評價研究。
三、主要業績:
主持中央高校基本科學業務專項項目一項,參與國家自然科學基金面上及重點等多項項目的研究;在國内外SCI期刊發表學術論文10餘篇。
四、 代表性研究成果
Wang Meimei, Yang Zhenyu, Song Yang, et al. Proteasomal and autophagy-mediated degradation of mutp53 proteins through mitochondria-targeting aggregation-induced-emission materials[J]. Acta Biomaterialia, 2022, 150: 402-412.
Wang Meimei, Ma Hang, Li Zhaoxing, et al. SPG-56 from Sweet potato Zhongshu-1 delayed growth of tumor xenografts in nude mice by modulating gut microbiota[J]. Journal of Functional Foods, 2019, 52: 291-301.
Wang Meimei, Ma Hang, Tian Cheng, et al. Bioassay-guided isolation of glycoprotein SPG-56 from sweet potato Zhongshu-1 and its anti-colon cancer activity in vitro and in vivo[J]. Journal of Functional Foods, 2017, 35: 315-324.
Tian Cheng, Wang Meimei, Liu Shanshan, et al. A new glycoprotein SPG-8700 isolated from sweet potato with potential anti-cancer activity against colon cancer[J]. Natural product research, 2019, 33(16): 2322-2328.
Jing Manman, Li Yafei, Wang Meimei, et al. Photoresponsive PAMAM‐Assembled Nanocarrier Loaded with Autophagy Inhibitor for Synergistic Cancer Therapy[J]. Small, 2021, 17(38): 2102295.
Ishimwe Nestor, Wei Pengfei, Wang Meimei, et al. Autophagy impairment through lysosome dysfunction by brucine induces immunogenic cell death (ICD)[J]. The American Journal of Chinese Medicine, 2020, 48(08): 1915-1940.
Ma Hang, Yu Yang, Wang Meimei, et al. Correlation between microbes and colorectal cancer: tumor apoptosis is induced by sitosterols through promoting gut microbiota to produce short-chain fatty acids[J]. Apoptosis, 2019, 24(1): 168-183.
Li Zhaoxing, Yu Yang, Wang Meimei, et al. Anti-breast cancer activity of SPG-56 from sweet potato in MCF-7 bearing mice in situ through promoting apoptosis and inhibiting metastasis[J]. Scientific reports, 2019, 9(1): 1-12.