دورية أكاديمية

[Influence of Qingdai compound on expression of bcr/abl and JWA in K562 cells].

التفاصيل البيبلوغرافية
العنوان: [Influence of Qingdai compound on expression of bcr/abl and JWA in K562 cells].
المؤلفون: Dai HP; Department of Hematology, The Jiangsu TCM Hospital, Nanjing TCM University, Nanjing 210029, China., Shen Q, Zhou JW, Tang WY, Zhu GR, Xia W
المصدر: Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2005 Oct; Vol. 13 (5), pp. 809-11.
نوع المنشور: Journal Article
اللغة: Chinese
بيانات الدورية: Publisher: Zhongguo shi yan xue za zhi she Country of Publication: China NLM ID: 101084424 Publication Model: Print Cited Medium: Print ISSN: 1009-2137 (Print) Linking ISSN: 10092137 NLM ISO Abbreviation: Zhongguo Shi Yan Xue Ye Xue Za Zhi Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Beijing : Zhongguo shi yan xue za zhi she,
مواضيع طبية MeSH: Apoptosis/*drug effects , Drugs, Chinese Herbal/*pharmacology , Fusion Proteins, bcr-abl/*genetics , Heat-Shock Proteins/*genetics , Intracellular Signaling Peptides and Proteins/*genetics, Antineoplastic Agents, Phytogenic/pharmacology ; Cell Proliferation/drug effects ; Dose-Response Relationship, Drug ; Gene Expression Regulation, Neoplastic/drug effects ; Humans ; K562 Cells ; Membrane Transport Proteins ; RNA, Messenger/biosynthesis ; RNA, Messenger/genetics ; Reverse Transcriptase Polymerase Chain Reaction
مستخلص: To study the effects of Qingdai compound on proliferation and apoptosis of K562 cells, as well as the expression of bcr/abl and JWA mRNA, K562 cells were treated in culture with different concentrations of Qingdai compound (2.5, 5, 7.5, 10 and 20 mg/ml) and harvested at 24 hours. Then morphological changes were observed by light microscopy (LM); expressions of bcr/abl and JWA were detected with semi-quantitative RT-PCR. The results showed that morphological changes were observed as the increment of the Qingdai compound concentration. Inhibition effects on proliferation and apoptosis in K562 cells were seen. A concentration-dependent decreases were found in bcr-abl and JWA mRNA expression of K562 cells. Qingdai compound partially inhibited proliferation and induced apoptosis of K562 cells. Expressions of both bcr/abl and JWA, which took part in cell proliferation and apoptosis, were down-regulated in a dose dependent manner. In conclusion, Qingdai compound can partially inhibit the expressions of bcr/abl and JWA genes in K562 cells, and the clinical effect of Qingdai compound on CML may be associated with apoptosis of leukemic cells.
المشرفين على المادة: 0 (ARL6IP5 protein, human)
0 (Antineoplastic Agents, Phytogenic)
0 (Drugs, Chinese Herbal)
0 (Heat-Shock Proteins)
0 (Intracellular Signaling Peptides and Proteins)
0 (Membrane Transport Proteins)
0 (RNA, Messenger)
EC 2.7.10.2 (Fusion Proteins, bcr-abl)
R1R8QUL21Z (Qingdai compound)
تواريخ الأحداث: Date Created: 20051110 Date Completed: 20080905 Latest Revision: 20191210
رمز التحديث: 20221213
PMID: 16277847
قاعدة البيانات: MEDLINE