Kumbhakar Divya Vishambhar, Thakkar Lucky, Akhand Chetana, Sharaf Shehna, Vemuganti Geeta K
Stem Cell and Cancer Biology Laboratory, School of Medical Science, University of Hyderabad, Telangana, India.
Thakkar Consultancy Services, Janjgir, Chhattisgarh, India.
Front Oncol. 2025 Jun 6;15:1499283. doi: 10.3389/fonc.2025.1499283. eCollection 2025.
A cancer stem cell (CSC) is an immortal cell that is capable of self-renewal, continuous proliferation, differentiation into various cancer cell lineages, metastatic dissemination, tumorigenesis, maintaining tumor heterogeneity, and resistance to conventional treatments. Targeted therapies have made huge advances in the past few years, but resistance is still a major roadblock to their success, in addition to their life-threatening side effects. Progressive treatments are now available, including immunotherapies, CRISPR-Cas 9, sonodynamic therapy, chemodynamic therapy, antibody-drug nanoconjugates, cell-based therapies, gene therapy, and ferroptosis-based therapy, which have replaced surgery, chemotherapy, and radiotherapy for cancer treatment. The challenge is to develop targeted treatment strategies that are effective in eradicating CSCs, as they are resistant to anticancer drugs, causing treatment failure, relapse, and recurrence of cancer. An overview of the fundamental characteristics of CSCs, drug resistance, tumor recurrence, and signaling pathways as well as biomarkers associated with their metastatic potential of CSC is elucidated in this review. The regulatory frameworks for manufacturing and conducting clinical trials on cancer therapy are explicated. Furthermore, we summarize a variety of promising nanocarriers (NCs) that have been used directly and/or synergistic therapies coupled with the therapeutic drug of choice for the detection, targeting, and imaging of CSCs to surmount therapeutic resistance and stemness-related signaling pathways and eradicate CSCs, hence alleviating the limitation of conventional therapies. Nanoparticle-mediated ablation therapies (NMATs) are also being argued as a method for burning or freezing cancer cells without undergoing open surgery. Additionally, we discuss the recent clinical trials testing exosomes, CRISPR/Cas9, and nanodrugs, which have already received approval for several new technologies, while others are still in the early stages of testing. The objective of this review is to elucidate the advantages of nanocarriers in conquering cancer drug resistance and to discuss the most recent developments in this field.
癌症干细胞(CSC)是一种永生细胞,能够自我更新、持续增殖、分化为各种癌细胞谱系、发生转移扩散、引发肿瘤形成、维持肿瘤异质性并对传统治疗产生抗性。在过去几年中,靶向治疗取得了巨大进展,但除了具有危及生命的副作用外,耐药性仍是其成功的主要障碍。目前已有多种进阶治疗方法,包括免疫疗法、CRISPR-Cas 9、声动力疗法、化学动力疗法、抗体-药物纳米缀合物、细胞疗法、基因疗法和铁死亡疗法,这些方法已取代手术、化疗和放疗用于癌症治疗。挑战在于开发有效的靶向治疗策略以根除癌症干细胞,因为它们对抗癌药物具有抗性,会导致治疗失败、癌症复发和再发。本综述阐明了癌症干细胞的基本特征、耐药性、肿瘤复发、信号通路以及与其转移潜能相关的生物标志物。文中还阐述了癌症治疗制造和开展临床试验的监管框架。此外,我们总结了多种有前景的纳米载体(NCs),它们已被直接使用和/或与首选治疗药物联合用于癌症干细胞的检测、靶向和成像,以克服治疗抗性和与干性相关的信号通路并根除癌症干细胞,从而缓解传统疗法的局限性。纳米颗粒介导的消融疗法(NMATs)也被认为是一种无需进行开放手术即可烧灼或冷冻癌细胞的方法。此外,我们讨论了近期测试外泌体、CRISPR/Cas9和纳米药物的临床试验,其中一些新技术已获批,而其他仍处于早期测试阶段。本综述的目的是阐明纳米载体在克服癌症耐药性方面的优势,并讨论该领域的最新进展。