Laboratorio de Biología Celular del Cáncer, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Av. Lázaro Cárdenas s/n, Chilpancingo, GRO 39090, Mexico.
Instituto de Farmacobiología, Universidad de la Cañada, Teotitlán de Flores Magón, OAX 68540, Mexico.
Life Sci. 2022 Nov 1;308:120932. doi: 10.1016/j.lfs.2022.120932. Epub 2022 Sep 5.
Cancer is one of the leading causes of death in patients worldwide, where invasion and metastasis are directly responsible for this statement. Although cancer therapy has progressed in recent years, current therapeutic approaches are ineffective due to toxicity and chemoresistance. Therefore, it is essential to evaluate other treatment options, and natural products are a promising alternative as they show antitumor properties in different study models. This review describes the regulation of tissue inhibitors of metalloproteinases (TIMPs) expression and the role of flavonoids as molecules with the antitumor activity that targets TIMPs therapeutically. These inhibitors regulate tissue extracellular matrix (ECM) turnover; they inhibit matrix metalloproteinases (MMPs), cell migration, invasion, and angiogenesis and induce apoptosis in tumor cells. Data obtained in cell lines and in vivo models suggest that flavonoids are chemopreventive and cytotoxic against various types of cancer through several mechanisms. Flavonoids also regulate crucial signaling pathways such as focal adhesion kinase (FAK), phosphatidylinositol-3-kinase (PI3K)-Akt, signal transducer and activator of transcription 3 (STAT3), nuclear factor κB (NFκB), and mitogen-activated protein kinase (MAPK) involved in cancer cell migration, invasion, and metastasis. All these data reposition flavonoids as excellent candidates for use in cancer therapy.
癌症是全球患者死亡的主要原因之一,其中侵袭和转移是导致这一说法的直接原因。尽管近年来癌症治疗取得了进展,但由于毒性和化疗耐药性,目前的治疗方法仍不奏效。因此,评估其他治疗方案至关重要,而天然产物作为一种有前途的替代物,因为它们在不同的研究模型中表现出抗肿瘤特性。这篇综述描述了组织金属蛋白酶抑制剂(TIMPs)表达的调节以及类黄酮作为具有抗肿瘤活性的分子靶向 TIMPs 治疗的作用。这些抑制剂调节组织细胞外基质(ECM)的转化;它们抑制基质金属蛋白酶(MMPs)、细胞迁移、侵袭和血管生成,并诱导肿瘤细胞凋亡。在细胞系和体内模型中获得的数据表明,类黄酮通过多种机制对各种类型的癌症具有化学预防和细胞毒性作用。类黄酮还调节关键信号通路,如粘着斑激酶(FAK)、磷脂酰肌醇-3-激酶(PI3K)-Akt、信号转导和转录激活因子 3(STAT3)、核因子 κB(NFκB)和丝裂原激活蛋白激酶(MAPK),这些通路参与癌细胞迁移、侵袭和转移。所有这些数据都使类黄酮重新成为癌症治疗的优秀候选物。