• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Relationship of calcitonin mRNA expression to the differentiation state of HL 60 cells.

作者信息

Kiefer P, Bacher M, Pflüger K H

机构信息

Philipps-University Marburg, Department of Internal Medicine, Germany.

出版信息

Leuk Lymphoma. 1994 May;13(5-6):501-7. doi: 10.3109/10428199409049641.

DOI:10.3109/10428199409049641
PMID:7520792
Abstract

Raised plasma levels of immunoreactive human calcitonin (ihCT) can be found in patients with myeloid leukemia and seem to indicate a poor prognosis. High levels were found in acute undifferentiated and acute myeloblastic leukemia. To test whether CT expression could be a marker of myeloid differentiation, we used the promyelocytic leukemia cell line HL 60 which also expresses ihCT as a model system for myeloid differentiation. Exponentially growing HL 60 cells as well as differentiation induced HL 60 cells expressed a single 1.0 Kb CT transcript. The induction of HL 60 cell differentiation along the granulocytic lineage by DMSO or HMBA had no effect on the level of CT transcripts. Induction of monocytic/macrophagic differentiation by TPA resulted in a transient, about 10-fold elevated expression of CT steady state mRNA after 24 h. In contrast to TPA, induction of HL 60 cell differentiation along the monocytic pathway by Vit D3 had no detectable effect on the level of the CT in RNA expression at corresponding time points. These findings suggest that the transient induction of CT steady state mRNA expression by TPA is rather a direct effect of the phorbol ester than commitment along the monocytic line of differentiation.

摘要

相似文献

1
Relationship of calcitonin mRNA expression to the differentiation state of HL 60 cells.
Leuk Lymphoma. 1994 May;13(5-6):501-7. doi: 10.3109/10428199409049641.
2
Prothymosin alpha gene expression correlates with proliferation, not differentiation, of HL-60 cells.原胸腺素α基因表达与HL-60细胞的增殖而非分化相关。
Blood. 1993 Aug 15;82(4):1127-32.
3
Modulation of gene expression in the acute promyelocytic leukemia cell line NB4.急性早幼粒细胞白血病细胞系NB4中基因表达的调控
Leukemia. 1993 Nov;7(11):1817-23.
4
Regulation of the expression of enzymes involved in the replication of DNA in chemically induced monocytic/macrophagic differentiation of HL-60 leukemia cells.化学诱导HL-60白血病细胞单核细胞/巨噬细胞分化过程中DNA复制相关酶表达的调控
Leuk Res. 1998 Aug;22(8):697-703. doi: 10.1016/s0145-2126(98)00054-x.
5
M-CSF and 1,25 dihydroxy vitamin D3 synergize with 12-O-tetradecanoylphorbol-13-acetate to induce macrophage differentiation in acute promyelocytic leukemia NB4 cells.巨噬细胞集落刺激因子(M-CSF)和1,25-二羟基维生素D3与12-O-十四烷酰佛波醇-13-乙酸酯协同作用,诱导急性早幼粒细胞白血病NB4细胞向巨噬细胞分化。
Leukemia. 1994 Oct;8(10):1744-9.
6
Lineage directed HL-60 cell sublines as a model system for the study of early events in lineage determination of myeloid cells.
Leuk Res. 1990;14(11-12):979-88. doi: 10.1016/0145-2126(90)90111-l.
7
Distinct temporal patterns of defensin mRNA regulation during drug-induced differentiation of human myeloid leukemia cells.人髓系白血病细胞药物诱导分化过程中防御素mRNA调控的独特时间模式。
Blood. 1996 Jan 1;87(1):350-64.
8
Expression of the transforming growth factor alpha protooncogene in differentiating human promyelocytic leukemia (HL-60) cells.转化生长因子α原癌基因在人早幼粒细胞白血病(HL-60)细胞分化过程中的表达
Cancer Res. 1993 Jan 1;53(1):191-6.
9
All-trans retinoic acid reverses phorbol ester resistance in a human myeloid leukemia cell line.
Blood. 1994 Jan 15;83(2):490-6.
10
Apoptosis of human leukemic HL-60 cells induced to differentiate by phorbol ester treatment.佛波酯处理诱导人白血病HL-60细胞分化过程中的凋亡。
Leukemia. 1994 May;8(5):792-7.

引用本文的文献

1
NoBP, a nuclear fibroblast growth factor 3 binding protein, is cell cycle regulated and promotes cell growth.NoBP是一种核成纤维细胞生长因子3结合蛋白,受细胞周期调控并促进细胞生长。
Mol Cell Biol. 2001 Aug;21(15):4996-5007. doi: 10.1128/MCB.21.15.4996-5007.2001.