Shafi Sadat, Ahmed Faraha, Waheed Ayesha, Ahmad Syed Sufiyan, Khan Sana, Khan Mohammad Ahmed, Pottoo Faheem Hyder, Rabbani Syed Arman, Singh Shailja, Najmi Abul Kalam
Department of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi 110062, India.
Department of Pharmacology, College of Clinical Pharmacy, Imam Abdulrahman Bin Faisal University, Dammam 31441, Saudi Arabia.
Mini Rev Med Chem. 2024 Sep 13. doi: 10.2174/0113895575297312240903055926.
Considerable advancements have been made in breast cancer therapeutics in the past few decades. However, the advent of chemo-resistance and adverse drug reactions coupled with tumor metastasis and recurrence posed a serious threat to combat this lethal disease. Novel anti-cancer agents, as well as new therapeutic strategies, are needed to complement conventional breast cancer therapies. The quest for developing novel anti-cancer drugs caused an upsurge in exploring and harnessing natural compounds, especially phytochemicals. Various research groups have explored and documented the anti-cancer potential of wide variety of phytochemical groups including flavonoids (curcumin, kaempferol, myricetin, quercetin, naringenin, apigenin, genistein epigallocatechin gallate), stilbenes (resveratrol), carotenoids (crocin, lycopene, lutein), and anthraquinone (Emodin). However, low chemical stability, poor water solubility, and short systemic half-life impede their clinical utility. The implication of nano-technological approaches to decode the pharmacokinetic challenges associated with phytochemical usage, as well as selective drug targeting, have markedly enhanced the pre-clinical anti-cancer activity, thus aiding in their clinical translation. This review documented the recent advances in utilizing phytochemicals for breast cancer prevention and lipidbased nanotechnological approaches for circumventing their pharmacokinetic concerns to enhance their systemic availability, cytotoxicity, and targeted delivery against breast cancer alone as well as in combination with conventional therapeutic agents.
在过去几十年中,乳腺癌治疗取得了显著进展。然而,化疗耐药性和药物不良反应的出现,再加上肿瘤转移和复发,对战胜这种致命疾病构成了严重威胁。需要新型抗癌药物以及新的治疗策略来补充传统的乳腺癌治疗方法。开发新型抗癌药物的需求促使人们对天然化合物,尤其是植物化学物质的探索和利用热潮兴起。各个研究小组已经探索并记录了多种植物化学物质的抗癌潜力,包括黄酮类化合物(姜黄素、山奈酚、杨梅素、槲皮素、柚皮素、芹菜素、染料木黄酮、表没食子儿茶素没食子酸酯)、芪类化合物(白藜芦醇)、类胡萝卜素(藏红花素、番茄红素、叶黄素)和蒽醌类化合物(大黄素)。然而,化学稳定性低、水溶性差和全身半衰期短阻碍了它们的临床应用。纳米技术方法在解决与植物化学物质使用相关的药代动力学挑战以及选择性药物靶向方面的应用,显著增强了临床前抗癌活性,从而有助于它们的临床转化。本综述记录了利用植物化学物质预防乳腺癌以及基于脂质的纳米技术方法来解决其药代动力学问题以提高其全身可用性及细胞毒性,并单独或与传统治疗药物联合用于乳腺癌靶向递送方面的最新进展。