Department of Biochemistry, Faculty of Sciences, University of Agriculture, Faisalabad, 38040, Pakistan.
Shandong Provincial Key Laboratory of Glycoscience and Glycoengineering, School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, China.
Clin Transl Oncol. 2022 Mar;24(3):432-445. doi: 10.1007/s12094-021-02709-3. Epub 2021 Oct 5.
Natural products, especially polyphenols (phenolic acids, lignans, and stilbenes) are suggested to be more potent anticancer drugs because of their no or less adverse effects, excess availability, high accuracy, and secure mode of action. In the present review, potential anticancer mechanisms of action of some polyphenols including phenolic acids, lignans, and stilbenes are discussed based on clinical, epidemiological, in vivo, and in vitro studies. The emerging evidence revealed that phenolic acids, lignans, and stilbenes induced apoptosis in the treatment of breast (MCF-7), colon (Caco-2), lung (SKLU-1), prostate (DU-145 and LNCaP), hepatocellular (hepG-2), and cervical (A-431) cancer cells, cell cycle arrest (S/G/M/G-phases) in gastric (MKN-45 and MKN-74), colorectal (HCT-116), bladder (T-24 and 5637), oral (H-400), leukemic (HL-60 and MOLT-4) and colon (Caco-2) cancer cells, and inhibit cell proliferation against the prostate (PC-3), liver (LI-90), breast (T47D and MDA-MB-231), colon (HT-29 and Caco-2), cervical (HTB-35), and MIC-1 cancer cells through caspase-3, MAPK, AMPK, Akt, NF-κB, Wnt, CD95, and SIRT1 pathways. Based on accumulated data, we suggested that polyphenols could be considered as a viable therapeutic option in the treatment of cancer cells in the near future.
天然产物,尤其是多酚(酚酸、木脂素和芪类)因其不良反应少或无、丰富的供应、高准确性和安全的作用模式,被认为是更有效的抗癌药物。在本综述中,根据临床、流行病学、体内和体外研究,讨论了一些多酚(包括酚酸、木脂素和芪类)的潜在抗癌作用机制。新出现的证据表明,酚酸、木脂素和芪类在治疗乳腺癌(MCF-7)、结肠癌(Caco-2)、肺癌(SKLU-1)、前列腺癌(DU-145 和 LNCaP)、肝癌(hepG-2)和宫颈癌(A-431)细胞时诱导细胞凋亡,在胃癌(MKN-45 和 MKN-74)、结直肠癌(HCT-116)、膀胱癌(T-24 和 5637)、口腔癌(H-400)、白血病(HL-60 和 MOLT-4)和结肠癌(Caco-2)细胞中诱导细胞周期停滞(S/G/M/G 期),并通过 caspase-3、MAPK、AMPK、Akt、NF-κB、Wnt、CD95 和 SIRT1 通路抑制前列腺(PC-3)、肝(LI-90)、乳腺(T47D 和 MDA-MB-231)、结肠(HT-29 和 Caco-2)、宫颈(HTB-35)和 MIC-1 癌细胞的增殖。基于积累的数据,我们认为多酚类化合物在不久的将来可能被认为是治疗癌细胞的一种可行的治疗选择。
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