Faculty of Health Sciences, Balamand University, Beirut, Lebanon.
INSERM, National Institute of Health and Medical Research, Paris XI, Paris, France.
Clin Transl Oncol. 2023 Jul;25(7):2056-2068. doi: 10.1007/s12094-023-03115-7. Epub 2023 Feb 17.
Stem cell-based therapies have been foreshowed as a promising therapeutic approach for the treatment of several diseases. However, in the cancer context, results obtained from clinical studies were found to be quite limited. Deeply implicated in inflammatory cues, Mesenchymal, Neural, and Embryonic Stem Cells have mainly been used in clinical trials as a vehicle to deliver and stimulate signals in tumors niche. Although these stem cells have shown some therapeutical promises, they still face several challenges, including their isolation, immunosuppression potential, and tumorigenicity. In addition, regulatory and ethical concerns limit their use in several countries. Mesenchymal stem cells (MSC) have emerged as a gold standard adult stem cell medicine tool due to their distinctive characteristics, such as self-renewal and potency to differentiate into numerous cell types with lower ethical restrictions. Secreted extracellular vesicles (EVs), secretomes, and exosomes play a crucial role in mediating cell-to-cell communication to maintain physiological homeostasis and influence pathogenesis. Due to their low immunogenicity, biodegradability, low toxicity, and ability to transfer bioactive cargoes across biological barriers, EVs and exosomes were considered an alternative to stem cell therapy through their immunological features. MSCs-derived EVs, exosomes, and secretomes showed regenerative, anti-inflammatory, and immunomodulation properties while treating human diseases. In this review, we provide an overview of the paradigm of MSCs derived exosomes, secretome, and EVs cell-free-based therapies, we will focus on MSCs-derived components in anti-cancer treatment with decreased risk of immunogenicity and toxicity. Astute exploration of MSCs may lead to a new opportunity for efficient therapy for patients with cancer.
基于干细胞的疗法被预测为治疗多种疾病的有前途的治疗方法。然而,在癌症领域,从临床研究中获得的结果被发现相当有限。间充质干细胞、神经干细胞和胚胎干细胞深深涉及炎症线索,主要被用于临床试验作为一种载体,在肿瘤微环境中传递和刺激信号。尽管这些干细胞显示出一些治疗潜力,但它们仍然面临着几个挑战,包括它们的分离、免疫抑制潜力和致瘤性。此外,监管和伦理问题限制了它们在许多国家的使用。间充质干细胞(MSC)因其独特的特性,如自我更新和分化为多种细胞类型的能力,而成为一种黄金标准的成人干细胞药物工具,这些特性受到的伦理限制较低。分泌的细胞外囊泡(EVs)、分泌组和外泌体在介导细胞间通讯以维持生理平衡和影响发病机制方面发挥着关键作用。由于其低免疫原性、生物降解性、低毒性和传递生物活性货物穿过生物屏障的能力,EVs 和外泌体因其免疫特性被认为是干细胞治疗的替代方法。MSC 衍生的 EVs、外泌体和分泌组在治疗人类疾病时表现出再生、抗炎和免疫调节特性。在这篇综述中,我们提供了 MSCs 衍生的外泌体、分泌组和 EVs 无细胞治疗范例的概述,我们将重点介绍 MSCs 衍生成分在降低免疫原性和毒性风险的抗癌治疗中的作用。对 MSCs 的敏锐探索可能为癌症患者提供高效治疗的新机会。