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Neuroblastoma Treatment Using Gene Therapy

机译:使用基因治疗的神经母细胞瘤治疗

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Neuroblastoma is a type of pediatric malignancy, characterised by high clinical heterogeneity. It starts from primitive nerve cells found in areas where nerves join together. The tumor regresses spontaneously in infants and on maturation differentiates into benign ganglioneuroblastoma in later stages. The tumor is peripheral and generally present on the sympathethic nervous system. In most of the solid tumors, tumor initiating cells (TICs) are present, which helps in fuelling the growth of tumor and start the metastases. Neuroblastoma typically spreads to the regional lymph nodes, bone and bone marrow. The mean age of diagnosis is 2 years, almost 1/4th of the cases occur before the age of 1 year and the remaining occur before 10 years of age. Symptoms generally depend on the size, location of the original tumor and extent to spread to the other parts of the body. Some prominent symptoms are pain, high blood pressure, problem in the movement of lower limb. Mostly in children it is recognized by the presence of an unusual lump in any part of the body (mainly abdominal region). Presence of common DNA variations in a region of chromosome 6 raises the risk of aggressive form of neuroblastoma in the child. Further sequencing of the chromosome region identified mutations in the anaplastic lymphoma kinase (ALK) gene in families affected by neuroblastoma. The epigenetic structure of DNA and its lesions play a role in the origin of human neuroblastomas due to which other treatment options for neuroblastomas can be created by the pharmaceutical manipulation of the epigenome. Cold atmospheric plasma (CAP) can be used as a treatment option for neuroblastoma since apoptosis can be induced in neuroblastoma cells using CAP. It also inhibits the metabolic rate of neuroblastoma cells.
机译:神经母细胞瘤是一种儿科恶性肿瘤,其特征在于临床异质性。它从神经连接在一起的区域发现的原始神经细胞。肿瘤在婴儿和成熟中自发地消退,在后期阶段分化为良性甘肝细胞瘤。肿瘤是外周性,通常存在于伴随的神经系统上。在大多数实体瘤中,存在肿瘤引发细胞(TICS),这有助于促进肿瘤的生长并开始转移。神经母细胞瘤通常蔓延到区域淋巴结,骨和骨髓。平均诊断年龄是2年,近1/4的病例发生在1年前,剩余发生在10岁之前。症状一般取决于尺寸,原始肿瘤的位置和范围蔓延到身体的其他部位。一些突出的症状是疼痛,高血压,下肢运动中的问题。主要是在儿童中,它是通过在身体(主要是腹部区域)的任何部位存在异常肿块的认可。染色体6区域的常见DNA变化引起了孩子中神经母细胞瘤的侵略性形式的风险。染色体区域的进一步测序鉴定受神经母细胞瘤影响的家族中的包塑淋巴瘤激酶(ALK)基因中的突变。 DNA及其病变的表观遗传结构在人类神经细胞瘤的起源中发挥作用,因为可以通过外延蛋白的药物操纵产生神经细胞瘤的其他治疗选择。冷大气等离子体(盖子)可用作神经母细胞瘤的治疗选择,因为凋亡可以使用帽诱导神经母细胞瘤细胞。它还抑制神经母细胞瘤细胞的代谢率。

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