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JB/MS 小鼠黑色素瘤:一种用于研究分化调节以及致瘤和转移潜能的新模型。

JB/MS murine melanoma: a new model for studies on the modulation of differentiation and of tumorigenic and metastatic potential.

作者信息

Hearing V J, Cannon G B, Vieira W D, Jiménez-Atiénzar M, Kameyama K, Law L W

机构信息

Laboratory of Cell Biology, National Cancer Institute, Bethesda, MD 20892.

出版信息

Int J Cancer. 1988 Feb 15;41(2):275-82. doi: 10.1002/ijc.2910410219.

Abstract

The recently obtained JB/MS melanoma (induced by DMBA in C57Bl/6 mice) has been successfully established in culture, and characterization of various parameters of these cells, as they have been serially passaged in vivo and in vitro, has begun. The culture lines were initially highly dendritic and melanotic, growing slowly in vitro and extremely slowly in vivo. During serial passage in vivo and in vitro the cell lines have gradually evolved into less melanotic, but more proliferative, tumorigenic and metastatic cells. We have been able to demonstrate that the JB/MS melanoma shares the common melanoma TSTA previously reported for B16, K1735 and JB/RH melanomas, but does not cross-react with the S91 melanoma or with other non-melanoma cell lines used as specificity controls. The JB/MS cells can be induced to differentiate in vitro by alpha-melanocyte stimulating hormone, a physiologically relevant agent, and studies have been initiated to detail the level at which this induction occurs. These sublines should prove to be excellent models for study of the progression of transformed cells from non-tumorigenic to tumorigenic phenotypes, and for progression through stages of varying metastatic potential, immunogenicity and differentiation.

摘要

最近获得的 JB/MS 黑色素瘤(由二甲基苯并蒽在 C57Bl/6 小鼠中诱导产生)已成功建立细胞培养体系,并且已经开始对这些细胞在体内和体外连续传代过程中的各种参数进行表征。培养细胞系最初具有高度树突状且富含黑色素,在体外生长缓慢,在体内生长极其缓慢。在体内和体外连续传代过程中,细胞系逐渐演变成黑色素含量减少但增殖性、致瘤性和转移性增强的细胞。我们已经能够证明,JB/MS 黑色素瘤与先前报道的 B16、K1735 和 JB/RH 黑色素瘤具有共同的黑色素瘤肿瘤特异性移植抗原(TSTA),但与 S91 黑色素瘤或用作特异性对照的其他非黑色素瘤细胞系无交叉反应。JB/MS 细胞可被生理相关因子α-黑素细胞刺激素诱导在体外分化,并且已经开始研究这种诱导发生的具体水平。这些亚系应被证明是研究转化细胞从非致瘤表型向致瘤表型进展以及通过不同转移潜能、免疫原性和分化阶段进展的优秀模型。

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