Lee Young-Shin, Kwon Ryuk Jun, Lee Hye Sun, Chung Jae Heun, Kim Yun Seong, Jeong Han-Sol, Park Su-Jung, Lee Seung Yeon, Kim Taehwa, Yoon Seong Hoon
Family Medicine Clinic and Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Republic of Korea.
Division of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Pharmaceutics. 2024 Dec 26;17(1):22. doi: 10.3390/pharmaceutics17010022.
Lung cancer remains a major global health problem because of its high cancer-related mortality rate despite advances in therapeutic approaches. Non-small cell lung cancer (NSCLC), a major subtype of lung cancer, is more amenable to surgical intervention in its early stages. However, the prognosis for advanced NSCLC remains poor, owing to limited treatment options. This underscores the growing need for novel therapeutic strategies to complement existing treatments and improve patient outcomes. In recent years, pentacyclic triterpenoids, a group of natural compounds, have emerged as promising candidates for cancer therapy due to their anticancer properties. Pentacyclic triterpenoids, such as lupeol, betulinic acid, betulin, oleanolic acid, ursolic acid, glycyrrhetinic acid, glycyrrhizin, and asiatic acid, have demonstrated the ability to inhibit cell proliferation and angiogenesis, induce apoptosis, suppress metastasis, and modulate inflammatory and immune pathways in NSCLC cell line models. These compounds exert their effects by modulating important signaling pathways such as NF-κB, PI3K/Akt, and MAPK. Furthermore, advances in drug delivery technologies such as nanocarriers and targeted delivery systems have improved the bioavailability and therapeutic efficacy of triterpenoids. However, despite promising preclinical data, rigorous clinical trials are needed to verify their safety and efficacy. This review explores the role of triterpenoids in NSCLC and therapeutic potential in preclinical models, focusing on their molecular mechanisms of action.
尽管治疗方法有所进步,但肺癌因其与癌症相关的高死亡率仍然是一个主要的全球健康问题。非小细胞肺癌(NSCLC)是肺癌的主要亚型,在早期更适合手术干预。然而,由于治疗选择有限,晚期NSCLC的预后仍然很差。这凸显了对新型治疗策略的需求日益增长,以补充现有治疗方法并改善患者预后。近年来,五环三萜类化合物作为一类天然化合物,因其抗癌特性已成为癌症治疗的有希望的候选药物。五环三萜类化合物,如羽扇豆醇、桦木酸、桦木醇、齐墩果酸、熊果酸、甘草次酸、甘草酸和积雪草苷,已在NSCLC细胞系模型中显示出抑制细胞增殖和血管生成、诱导细胞凋亡、抑制转移以及调节炎症和免疫途径的能力。这些化合物通过调节重要的信号通路如NF-κB、PI3K/Akt和MAPK发挥作用。此外,纳米载体和靶向递送系统等药物递送技术的进步提高了三萜类化合物的生物利用度和治疗效果。然而,尽管临床前数据很有前景,但仍需要严格的临床试验来验证其安全性和有效性。本综述探讨了三萜类化合物在NSCLC中的作用以及在临床前模型中的治疗潜力,重点关注其分子作用机制。