P19一种Parthenin类似物在急性淋巴细胞白血病细胞中诱导细胞系依赖性凋亡和免疫调节信号传导。

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL International Journal of Molecular and Cellular Medicine Pub Date : 2023-01-01 DOI:10.22088/IJMCM.BUMS.12.1.1
Vishal Sharma, Samriti Dhawan, Ajay Kumar, Jagdeep Kaur
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引用次数: 0

摘要

白血病是一种影响血液和骨髓的癌症。急性淋巴细胞白血病,也被称为ALL,被认为是癌症最致命的形式之一。由于各种癌症病例的快速增加和癌症细胞耐药性的发展,有必要鉴定具有更有效抗癌特性的新型先导分子。人们对使用草药产品/类似物作为多组分药物(作为抗癌剂和免疫调节剂)治疗癌症越来越感兴趣。在本研究中,已经尝试探索P19的抗癌和免疫调节活性,P19是parthenin在ALL中的类似物。据报道,P19通过显著的NO产生触发人白血病HL-60细胞中的凋亡信号事件而表现出抗癌功效。与这一发现相反,P19介导的Raji细胞凋亡不需要ROS和NO。观察到P19的作用机制是癌症细胞谱系依赖性的。P19对ALL表现出非常有效的抗癌特性(IC50 3µM)。分子研究表明,P19通过Bax定位于线粒体并增强细胞质中的胞浆钙来诱导线粒体介导的细胞凋亡。caspase 3、caspase 8和PARP切割的进一步激活表明参与了caspase介导的细胞凋亡。抗增殖活性显示P19治疗后端粒酶抑制和细胞周期阻滞在G0/G1期。P19的免疫调节作用显示Jurkat和THP细胞中INF和NO的产生增强。由于其对白血病细胞的抗增殖和免疫调节潜力,P19可以被进一步探索为对白血病的有效治疗方法。
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P19 a Parthenin Analog Induces Cell Lineage Dependent Apoptotic and Immunomodulatory Signaling in Acute Lymphoid Leukemia Cells.

Leukemia is a type of cancer that affects the blood and bone marrow. Acute lymphoid leukaemia, also known as ALL, is regarded as one of the deadliest forms of cancer. Due to the rapid increase in various cancer cases and the development of resistance in cancer cells, it is necessary to identify novel lead molecules with more potent anticancer properties. There is a growing interest in using herbal products/analogs as multi-component agents (as anticancer agents and immunomodulators) for cancer treatment. In the present investigation, an attempt has been made to explore the anticancer and immunomodulatory activity of P19, an analog of parthenin in ALL. P19 was reported to exhibit anticancer efficacy by triggering apoptotic signaling events in human leukaemia HL-60 cells by significant NO production. In contrast to this finding, ROS and NO were not required for P19-mediated apoptosis in Raji cells. The mechanism of action of P19 was observed to be cancer cell lineage dependent. P19 demonstrated very effective anticancer properties against ALL (IC50 3µM). Molecular investigations revealed that P19 induced mitochondrion mediated apoptosis by Bax localization to mitochondria and enhanced cytosolic calcium in the cytoplasm. Further activation of the caspase 3, caspase 8 and PARP cleavage suggested the involvement of the caspase-mediated apoptosis. Anti-proliferative activity revealed the telomerase inhibition and cell cycle arrest in G0/G1 phase after P19 treatment. Immunomodulatory effects of the P19 revealed the enhanced INFɣ and NO production in Jurkat and THP cells. Owing to its antiproliferative and immunomodulatory potential against leukemia cells P19 can further be explored as effective therapeutics against leukemia.

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期刊介绍: The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).
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