Stem Cell Research & Application Center, Ondokuz Mayıs University, Kurupelit Campus, 55139, Atakum, Samsun, Turkey.
Appl Biochem Biotechnol. 2024 Jul;196(7):4105-4124. doi: 10.1007/s12010-023-04757-7. Epub 2023 Oct 28.
Mesenchymal stem cells (MSCs) are promising biological therapeutic candidates in cancer treatment. As a source of MSCs, palatine tonsil tissue is one of the secondary lymphoid organs that form an essential part of the immune system, and the relation between the secondary lymphoid organs and cancer progression leads us to investigate the effect of tonsil-derived MSCs (T-MSC) on cancer treatment. We aimed to determine the anti-tumoral effects of T-MSCs cultured at the febrile temperature (40 °C) on hematological cancer cell lines. The co-culture of cancer cells with T-MSCs was carried out under fever and normal culture conditions, and then the cell viability was determined by cell counting. In addition, apoptosis rate and cell cycle arrest were determined by flow cytometry. We confirmed the apoptotic effect of T-MSC co-culture at the transcriptional level by using real-time polymerase chain reaction (RT-PCR). We found that co-culture of cancer cells with T-MSCs significantly decreased the viable cell number under the febrile and normal culture conditions. Besides, the T-MSC co-culture induced apoptosis on K562 and MOLT-4 cells and induced the cell cycle arrest at the G2/M phase on MOLT-4 cells. The apoptotic effect of T-MSC co-culture under febrile stimulation was confirmed at the transcriptional level. Our study has highlighted the anti-tumoral effect of the cellular interaction between the T-MSCs and human hematological cancer cells during in vitro co-culture under hyperthermia.
间充质干细胞(MSCs)是癌症治疗中有前途的生物治疗候选物。作为 MSC 的来源之一,扁桃体组织是次级淋巴器官之一,是免疫系统的重要组成部分,次级淋巴器官与癌症进展之间的关系促使我们研究扁桃体来源的间充质干细胞(T-MSC)对癌症治疗的影响。我们旨在确定在发热温度(40°C)下培养的 T-MSCs 对血液癌细胞系的抗肿瘤作用。在发热和正常培养条件下将癌细胞与 T-MSCs 共培养,然后通过细胞计数测定细胞活力。此外,通过流式细胞术测定细胞凋亡率和细胞周期停滞。我们通过实时聚合酶链反应(RT-PCR)在转录水平证实了 T-MSC 共培养的凋亡作用。我们发现,在发热和正常培养条件下,癌细胞与 T-MSCs 的共培养显著降低了活细胞数量。此外,T-MSC 共培养诱导 K562 和 MOLT-4 细胞凋亡,并诱导 MOLT-4 细胞的细胞周期停滞在 G2/M 期。发热刺激下 T-MSC 共培养的凋亡作用在转录水平得到证实。我们的研究强调了 T-MSCs 与人类血液癌细胞之间的细胞相互作用在高热体外共培养下的抗肿瘤作用。