中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Lasiokaurin Regulates PLK1 to Induce Breast Cancer Cell G2/M Phase Block and Apoptosis

文献类型:期刊论文

作者Liu, Zhengrui3,4; Wang, Jia3,4; Xie, Siman3,4; Zhang, Benteng3,4; Yuan, Yan3,4; Fu, Huaizi3,4; Hao, Hongyun3,4; Sun, Li3,4; Yuan, Shengtao3,4; Ding, Jian2
刊名JOURNAL OF CANCER
出版日期2024
卷号15期号:8页码:2318-2328
关键词Lasiokaurin breast cancer G2/M phase block apoptosis PLK1
ISSN号1837-9664
DOI10.7150/jca.93621
通讯作者Ding, Jian(jding@simm.ac.cn) ; Yu, Hong(yuhong@njmu.edu.cn) ; Yang, Mei(yangmei@cpu.edu.cn)
英文摘要Aim of the study: To investigate the anti -tumor effects of Lasiokaurin on breast cancer and explore its underlying molecular mechanism. Materials and methods: In this study, MTT assay, plate colony formation assays, soft agar assay, and EdU assay were employed to evaluate the anti -proliferation effects of LAS. Apoptosis and cell cycle distribution were detected by flow cytometry. The molecular mechanism was predicted by performing RNA sequencing and verified by using immunoblotting assays. Breast cancer organiods derived from patient -derived xenografts model and MDA-MB-231 xenograft mouse model were established to assess the effect of LAS. Results: Our study showed that LAS treatment significantly suppressed cell viability of 5 breast cancer cell lines, with the IC 50 value of approximately 1-5 mu M. LAS also inhibitied the clonogenic ability and DNA synthesis of breast cancer cells, Moreover, LAS induced apoptosis and G2/M cell cycle arrest in SK -BR -3 and MDA-MB-231 cells. Notably, transcriptomic analysis predicted the mechanistic involvement of PLK1 in LAS -suppressed breast cancer progression. Our experiment data further verified that LAS reduced PLK1 mRNA and protein expression in breast cancer, accompanied by downregulating CDC25C and AKT phosphorylation. Ultimately, we confirmed that LAS inhibit breast cancer growth via inhibiting PLK1 pathway in vivo. Conclusions: Collectively, our findings revealed that LAS inhibits breast cancer progression via regulating PLK1 pathway, which provids scientific evidence for the use of traditional Chinese medicine in cancer therapy.
WOS关键词KINASE 1 ; DITERPENOIDS ; CYCLE ; PHOSPHORYLATION ; INHIBITION ; STATISTICS ; RUBESCENS ; PROTEIN
资助项目Jiangsu Funding Program for Excellent Postdoctoral Talent[1412200065]
WOS研究方向Oncology
语种英语
WOS记录号WOS:001255874700017
出版者IVYSPRING INT PUBL
源URL[http://119.78.100.183/handle/2S10ELR8/312044]  
专题中国科学院上海药物研究所
通讯作者Ding, Jian; Yu, Hong; Yang, Mei
作者单位1.Nanjing Med Univ, Affiliated Taizhou Peoples Hosp, Dept Pathol, Taizhou, Jiangsu, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai, Peoples R China
3.China Pharmaceut Univ, Natl Key Lab Multitarget Nat Drugs, Nanjing, Peoples R China
4.China Pharmaceut Univ, Jiangsu Key Lab Drug Screening, Nanjing, Peoples R China
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GB/T 7714
Liu, Zhengrui,Wang, Jia,Xie, Siman,et al. Lasiokaurin Regulates PLK1 to Induce Breast Cancer Cell G2/M Phase Block and Apoptosis[J]. JOURNAL OF CANCER,2024,15(8):2318-2328.
APA Liu, Zhengrui.,Wang, Jia.,Xie, Siman.,Zhang, Benteng.,Yuan, Yan.,...&Yang, Mei.(2024).Lasiokaurin Regulates PLK1 to Induce Breast Cancer Cell G2/M Phase Block and Apoptosis.JOURNAL OF CANCER,15(8),2318-2328.
MLA Liu, Zhengrui,et al."Lasiokaurin Regulates PLK1 to Induce Breast Cancer Cell G2/M Phase Block and Apoptosis".JOURNAL OF CANCER 15.8(2024):2318-2328.

入库方式: OAI收割

来源:上海药物研究所

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