Telang Nitin T
Cancer Prevention Research Program, Palindrome Liaisons Consultants, Montvale, NJ 07645-1559, USA.
Int J Mol Sci. 2025 Mar 12;26(6):2529. doi: 10.3390/ijms26062529.
Long-term treatment options for conventional chemo-endocrine therapy and molecular-pathway-based targeted therapy are associated with acquired therapy resistance and the emergence of drug-resistant cancer-initiating stem cell populations, leading to the progression of metastatic disease. These treatment options are based on the expression status of estrogen receptor-α (ER-α), progesterone receptor (PR) hormone receptors, and/or of human epidermal growth factor receptor-2 (HER-2). The breast cancer subtypes Luminal A, Luminal B, and HER-2-enriched express hormone/growth factor receptors and exhibit a favorable response to hormone receptor modulators and growth factor receptor antagonists. The triple-negative breast cancer subtype lacks the expression of hormone/growth factor receptors and responds only to cytotoxic conventional chemotherapy. The clinical limitations, due to the modest therapeutic responses of chemo-resistant cancer-initiating stem cells, emphasize the need for the identification of stem cells targeting testable alternatives for therapy-resistant breast cancer. Developed drug-resistant stem cell models exhibit upregulated expression of select cellular biomarker tumor spheroid (TS) formations and cluster of differentiation44 (CD44), DNA-binding protein (NANOG), and octamer-binding protein-4 (OCT-4) molecular biomarkers that represent novel experimentally modifiable quantitative endpoints. Naturally occurring dietary phytochemicals and nutritional herbs containing polyphenols, flavones, terpenes, saponins, lignans, and tannins have documented human consumption, lack systemic toxicity, lack phenotypic drug resistance, and exhibit preclinical efficacy. Constituent bioactive agents may provide testable stem cell-targeting alternatives. The present report provides an overview of (i) clinically relevant cellular models and drug-resistant cancer stem cell models for breast cancer subtypes, (ii) evidence for preclinical efficacy and mechanistic leads for natural phytochemicals and nutritional herbs, and (iii) the potential for the stem cell-targeting efficacy of natural bioactive agents as testable drug candidates for therapy-resistant breast cancer.
传统化学内分泌疗法和基于分子途径的靶向疗法的长期治疗方案与获得性治疗耐药性以及耐药性癌症起始干细胞群体的出现相关,从而导致转移性疾病的进展。这些治疗方案基于雌激素受体-α(ER-α)、孕激素受体(PR)激素受体和/或人表皮生长因子受体-2(HER-2)的表达状态。乳腺癌亚型Luminal A、Luminal B和HER-2富集型表达激素/生长因子受体,并对激素受体调节剂和生长因子受体拮抗剂表现出良好反应。三阴性乳腺癌亚型缺乏激素/生长因子受体的表达,仅对细胞毒性传统化疗有反应。由于化疗耐药性癌症起始干细胞的治疗反应有限,临床局限性凸显了识别针对耐药性乳腺癌的可测试替代疗法的干细胞的必要性。已建立的耐药干细胞模型显示,特定细胞生物标志物肿瘤球(TS)形成以及分化簇44(CD44)、DNA结合蛋白(NANOG)和八聚体结合蛋白-4(OCT-4)分子生物标志物的表达上调,这些代表了新的可通过实验修改的定量终点。含有多酚、黄酮、萜类、皂苷、木脂素和单宁的天然膳食植物化学物质和营养草药已有人类食用记录,缺乏全身毒性,没有表型耐药性,并具有临床前疗效。其成分生物活性剂可能提供可测试的靶向干细胞的替代方案。本报告概述了:(i)乳腺癌亚型的临床相关细胞模型和耐药性癌症干细胞模型;(ii)天然植物化学物质和营养草药的临床前疗效证据和作用机制线索;(iii)天然生物活性剂作为耐药性乳腺癌可测试候选药物的靶向干细胞疗效的潜力。