Therapeutic Potential of Luteolin on Cancer

被引:82
作者
cetinkaya, Melisa [1 ]
Baran, Yusuf [1 ]
机构
[1] Izmir Inst Technol, Fac Sci, Dept Mol Biol & Genet, TR-35430 Izmir, Turkiye
关键词
flavonoids; Luteolin; anticancer; apoptosis; cell cycle regulation; angiogenesis; metastasis; combination therapy; nanodelivery systems; miRNAs; APOPTOTIC CELL-DEATH; ACTIVATED PROTEIN-KINASE; NEGATIVE BREAST-CANCER; MESENCHYMAL TRANSITION; DIETARY FLAVONOIDS; SIGNALING PATHWAYS; ANTITUMOR-ACTIVITY; COLORECTAL-CANCER; INHIBITS INVASION; MDA-MB-231; CELLS;
D O I
10.3390/vaccines11030554
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cancer is a global concern, as the rate of incidence is increasing each year. The challenges related to the current chemotherapy drugs, such as the concerns related to toxicity, turn to cancer therapeutic research to discover alternative therapy strategies that are less toxic to normal cells. Among those studies, the use of flavonoids-natural compounds produced by plants as secondary metabolites for cancer therapy-has been a hot topic in cancer treatment. Luteolin, a flavonoid that has been present in many fruits, vegetables, and herbs, has been identified to exhibit numerous biological activities, including anti-inflammatory, antidiabetic, and anticancer properties. The anticancer property of Luteolin has been extensively researched in many cancer types and has been related to its ability to inhibit tumor growth by targeting cellular processes such as apoptosis, angiogenesis, migration, and cell cycle progression. It achieves this by interacting with various signaling pathways and proteins. In the current review, the molecular targets of Luteolin as it exerts its anticancer properties, the combination therapy that includes Luteolin with other flavonoids or chemotherapeutic drugs, and the nanodelivery strategies for Luteolin are described for several cancer types.
引用
收藏
页数:30
相关论文
共 150 条
[1]   Apoptosis induced by luteolin in breast cancer: Mechanistic and therapeutic perspectives [J].
Ahmed, Salman ;
Khan, Haroon ;
Fratantonio, Deborah ;
Hasan, Muhammad Mohtasheemul ;
Sharifi, Simin ;
Fathi, Nazanin ;
Ullah, Hammad ;
Rastrelli, Luca .
PHYTOMEDICINE, 2019, 59
[2]   Luteolin-Loaded Elastic Liposomes for Transdermal Delivery to Control Breast Cancer: In Vitro and Ex Vivo Evaluations [J].
Altamimi, Mohammad A. ;
Hussain, Afzal ;
AlRajhi, Mohammad ;
Alshehri, Sultan ;
Imam, Syed Sarim ;
Qamar, Wajhul .
PHARMACEUTICALS, 2021, 14 (11)
[3]  
[Anonymous], 2013, J CHEM PHARM RES
[4]   Luteolin Decreases Epidermal Growth Factor Receptor-Mediated Cell Proliferation and Induces Apoptosis in Glioblastoma Cell Lines [J].
Anson, David M. ;
Wilcox, Rachel M. ;
Huseman, Eric D. ;
Stump, Trevor A. ;
Paris, Robert L. ;
Darkwah, Belinda O. ;
Lin, Stacy ;
Adegoke, Andrea O. ;
Gryka, Rebecca J. ;
Jean-Louis, Denise S. ;
Amos, Samson .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2018, 123 (06) :678-686
[5]   Combined Curcumin and Luteolin Synergistically Inhibit Colon Cancer Associated with Notch1 and TGF-β Signaling Pathways in Cultured Cells and Xenograft Mice [J].
Aromokeye, Rukayat ;
Si, Hongwei .
CANCERS, 2022, 14 (12)
[6]   Anti-inflammatory effects of luteolin: A review of in vitro, in vivo, and in silico studies [J].
Aziz, Nur ;
Kim, Mi-Yeon ;
Cho, Jae Youl .
JOURNAL OF ETHNOPHARMACOLOGY, 2018, 225 :342-358
[7]   Plant Foods Rich in Antioxidants and Human Cognition: A Systematic Review [J].
Baroni, Luciana ;
Sarni, Anna Rita ;
Zuliani, Cristina .
ANTIOXIDANTS, 2021, 10 (05)
[8]   GENOMIC INSTABILITY IN CANCER Strategies to improve radiotherapy with targeted drugs [J].
Begg, Adrian C. ;
Stewart, Fiona A. ;
Vens, Conchita .
NATURE REVIEWS CANCER, 2011, 11 (04) :239-253
[9]   Paclitaxel: What has been done and the challenges remain ahead [J].
Bernabeu, Ezequiel ;
Cagel, Maximiliano ;
Lagomarsino, Eduardo ;
Moretton, Marcela ;
Chiappetta, Diego A. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 526 (1-2) :474-495
[10]   Dietary flavonoids, quercetin, luteolin and genistein, reduce oxidative DNA damage and lipid peroxidation and quench free radicals [J].
Cai, QY ;
Rahn, RO ;
Zhang, RW .
CANCER LETTERS, 1997, 119 (01) :99-107