人类B型淋巴细胞感染EBV的转化和血细胞分化由ras瘤基因
S Seremetis1, G Inghirami, D Ferrero
1Department of Pathology, New York University, NY 10016.
概括
在B细胞中Ras瘤基因的激活会导致恶性转变,并促进分化成血细胞,这是一个新发现,对B-淋巴细胞恶性瘤如多发性髓瘤有意义.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 免疫学 免疫学 免疫学
背景情况:
- 拉斯瘤基因在人类癌症中经常被激活.
- 在B细胞分化和恶性瘤中,ras瘤基因激活的作用尚未完全理解.
研究的目的:
- 研究H-和N-ras在人类B型淋巴细胞中的基激活的生物学影响.
- 确定ras瘤基因表达是否影响B细胞分化和恶性转变.
主要方法:
- 用复原病毒载体引入H或N-ras瘤基因到Epstein-Barr病毒不朽化的人类B型淋巴细胞中.
- 通过克隆原性测定和免疫缺陷小鼠的瘤原性评估恶性转变.
- 分析终端分化标记物,包括形态,免疫球蛋白分泌和细胞表面抗原表达.
主要成果:
- H-和N-ras瘤基因的表达诱导了B型淋巴细胞的恶性转变.
- 拉斯瘤基因的激活促进了终端分化成血细胞.
- 观察到的变化包括改变形态,增加免疫球蛋白分泌和修改细胞表面抗原表达.
结论:
- 拉斯瘤基因激活具有促进人类B型淋巴细胞生长和分化的新型双重效应.
- 这一发现提供了对终端分化的B-淋巴细胞恶性瘤,如多发性骨髓瘤的发病过程的见解.
相关概念视频
Abnormal Proliferation
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
The Ras Gene
The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
Ras is a superfamily...
Ras is a superfamily...
The Retinoblastoma Gene
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...


