Natural Products as Novel Therapeutic Agents for Triple-Negative Breast Cancer: Current Evidence, Mechanisms, Challenges, and Opportunities

被引:3
作者
Li, Qingzhou [1 ]
Ye, Zhen [2 ]
Wang, Guilin [2 ]
Chen, Yuhui [2 ]
Deng, Jinghong [2 ]
Wang, Dong [1 ,2 ]
Wang, Yumei [1 ,2 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Pharm, State Key Lab Southwestern Chinese Med Resources, Chengdu 611137, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Sch Basic Med Sci, Chengdu 611137, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
triple-negative breast cancer; herbal medicine; natural products; therapeutic strategies; mechanism; CELL-CYCLE ARREST; INHIBITS MIGRATION; MDA-MB-231; CELLS; IN-VIVO; ANTICANCER ACTIVITY; SIGNALING PATHWAY; GINSENOSIDE RG1; DOWN-REGULATION; APOPTOSIS; INVASION;
D O I
10.3390/molecules30061201
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Breast cancer (BC) tops the list of causes for female fatalities globally, with the elusive triple-negative breast cancer (TNBC) constituting 10-20% of all cases. Current clinical strategies for combating TNBC encompass a multifaceted approach, including surgical intervention, radiation therapy, chemotherapy, and advanced targeted drugs and immunotherapies. While these modalities have catalyzed significant advancements in TNBC management, lingering limitations continue to pose formidable challenges. There is an acute need for novel therapeutics in the realm of TNBC treatment. Natural products (NPs) have emerged as a rich reservoir for pharmaceutical innovation, owing to their extraordinary range of structures and physicochemical properties. Scholars have reported diverse evidence of NPs' efficacy against TNBC. This review aims to comprehensively explore the bioactive constituents, specifics and commonalities of chemical structure, and pharmacological mechanisms of NPs, specifically examining their multifaceted roles in impeding TNBC. NPs, which have recently garnered significant interest, are intriguing in terms of their capacity to combat TNBC through multifaceted mechanisms, including the suppression of tumor cell proliferation, the induction of apoptosis, and the inhibition of tumor metastasis. These natural agents primarily encompass a range of compounds, including terpenoids, glycosides, phenolic compounds, and alkaloids. An in-depth exploration has unveiled their involvement in key signaling pathways, including the transforming growth factor-beta (TGF-beta), vascular endothelial growth factor A (VEGFA), phosphoinositide 3-kinase/protein kinase B (PI3K/AKT), Wingless/Int-1 (Wnt) /beta-catenin, and mitogen-activated protein kinase (MAPK) pathways. Meanwhile, this review also looks at the challenges and opportunities that arise from harnessing natural compounds to influence TNBC, while outlining the prospective trajectory for future research in the field of NPs.
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页数:32
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共 183 条
[21]   Alantolactone selectively suppresses STAT3 activation and exhibits potent anticancer activity in MDA-MB-231 cells [J].
Chun, Jaemoo ;
Li, Rui-Juan ;
Cheng, Mao-Sheng ;
Kim, Yeong Shik .
CANCER LETTERS, 2015, 357 (01) :393-403
[22]   Platycodin D inhibits migration, invasion, and growth of MDA-MB-231 human breast cancer cells via suppression of EGFR-mediated Ala and MAPK pathways [J].
Chun, Jaemoo ;
Kim, Yeong Shik .
CHEMICO-BIOLOGICAL INTERACTIONS, 2013, 205 (03) :212-221
[23]   Relationship between VEGF Family Members, Their Receptors and Cell Death in the Neoplastic Transformation of Colorectal Cancer [J].
Dakowicz, Dominika ;
Zajkowska, Monika ;
Mroczko, Barbara .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (06)
[24]   The Role of the PI3K-AKT Pathway in Melanoma [J].
Davies, Michael A. .
CANCER JOURNAL, 2012, 18 (02) :142-147
[25]   Collateral Sensitivity of Parthenolide via NF-κB and HIF-α Inhibition and Epigenetic Changes in Drug-Resistant Cancer Cell Lines [J].
Dawood, Mona ;
Ooko, Edna ;
Efferth, Thomas .
FRONTIERS IN PHARMACOLOGY, 2019, 10
[26]   Targeting FAK in anticancer combination therapies [J].
Dawson, John C. ;
Serrels, Alan ;
Stupack, Dwayne G. ;
Schlaepfer, David D. ;
Frame, Margaret C. .
NATURE REVIEWS CANCER, 2021, 21 (05) :313-324
[27]   Berberine Attenuates Cell Motility via Inhibiting Inflammation-Mediated Lysyl Hydroxylase-2 and Glycolysis [J].
Du, Yishan ;
Khan, Muhammad ;
Fang, Nana ;
Ma, Fang ;
Du, Hongzhi ;
Tan, Zhenya ;
Wang, Hua ;
Yin, Shi ;
Wei, Xiaohui .
FRONTIERS IN PHARMACOLOGY, 2022, 13
[28]   Cucurbitacin B inhibits human breast cancer cell proliferation through disruption of microtubule polymerization and nucleophosmin/B23 translocation [J].
Duangmano, Suwit ;
Sae-lim, Phorntip ;
Suksamrarn, Apichart ;
Domann, Frederick E. ;
Patmasiriwat, Pimpicha .
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2012, 12
[29]   Norstictic Acid Inhibits Breast Cancer Cell Proliferation, Migration, Invasion, and In Vivo Invasive Growth Through Targeting C-Met [J].
Ebrahim, Hassan Y. ;
Elsayed, Heba E. ;
Mohyeldin, Mohamed M. ;
Akl, Mohamed R. ;
Bhattacharjee, Joydeep ;
Egbert, Susan ;
El Sayed, Khalid A. .
PHYTOTHERAPY RESEARCH, 2016, 30 (04) :557-566
[30]   The phloroglucinol calcitrinone A, a novel mitochondria-targeting agent, induces cell death in breast cancer cells [J].
El Gaafary, Menna ;
Saber, Fatema R. ;
Mahrous, Engy A. ;
Ashour, Rehab M. ;
Okba, Mona M. ;
Jin, Lu ;
Lang, Sophia J. ;
Schmiech, Michael ;
Simmet, Thomas ;
Syrovets, Tatiana .
FOOD AND CHEMICAL TOXICOLOGY, 2022, 162