|
|
| Research article summary (published 12 Nov 2006): |
[Primary application of spectral karyotyping in leukemia]
Full Abstract
OBJECTIVE:
To establish a spectral karyotyping (SKY) technique and explore the value of SKY in leukemia research.
METHODS:
SKY technique was conducted on 2 samples of peripheral blood from 2 healthy volunteers, then on the samples from 8 patients with leukemia, including chronic myelocytic leukemia (CML) and acute myelocytic leukemia (AML) confirmed by R-banding. In addition, four patients underwent dual fusion-fluorescence in situ hybridization (DF-FISH) to detect the mixed lineage leukemia (MLL), PML/RARa, and BCR/ABL fusion genes. By comparing the results of SKY, R-band karyotyping, and DF-FISH, the stability and reliability of SKY was judged.
RESULTS:
All 10 samples were successfully hybridized and karyotyped. The 2 cases of healthy volunteers showed normal karyotypes, thus, a specific SKY technique was successfully established. In the 8 cases of leukemia patients, SKY identified aberrations including 9q-, t (9; 22), t (15; 17) and the complex karyotype 47, XY, +9?ins (1;5) (q23;q23), t (6;7) (q23?; p13), in addition, the SKY technique detected some number abnormalities. The results of SKY confirmed the results of R-band karyotyping and DF-FISH; moreover, the SKY technique provided more accurate karyotypes.
CONCLUSION:
With high stability, accuracy, and sensitivity, the SKY technique established by this study can be applied in leukemia research.
Learn Faster Today Improve your study skills
Author information
Author/s: Guo, Bo (B); DA, Wan-ming (WM); Han, Xiao-ping (XP); Sun, Jing-fen (JF); Huang, Wen-rong (WR); Wang, Ke (K);
Affiliation: General Hospital of People's Liberation Army, Beijing 100853, China.
Journal and publication information
Publication Type: English Abstract; Journal Article
Journal: Zhonghua yi xue za zhi (Zhonghua Yi Xue Za Zhi), published in China. (Language: chi)
Reference: 2006-Nov; vol 86 (issue 42) : pp 2978-81
Dates: Created 2007/02/09; Completed 2008/05/05;
PMID: 17288810, status: MEDLINE (last retrieval date: 12/26/2008)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
External Links for this article (including full text providers, if available):
Click Electronic Full-text Provider Links to see options for finding the electronic full text links to this article. Note there may be a subscription or fee required for access to the full text. See our FAQ for information on finding FREE full text articles.
This article may also be located in paper journal collections available in many libraries. Use the Journal and Publication Information above to find the full article.
MeSH headings (categories)
This article was linked to the MESH Headings shown below.
|
Related articles
These are the highest related articles currently in the database:
- Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.
30 Mar 2006 - A case of acute myelogenous leukemia with MLL-AF10 fusion caused by insertion of 5' MLL into 10p12, with concurrent 3' MLL deletion.
30 Oct 2006 - Multicolor karyotyping and clinicopathological analysis of three intravascular lymphoma cases.
29 Jun 2003 - Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sézary syndrome: search for recurrent chromosome abnormalities.
30 Mar 2006 - Evaluation of spectral karyotyping (SKY) in biodosimetry for the triage situation following gamma irradiation.
30 Jan 2006 - Rapid localization of transgenes in mouse chromosomes with a combined Spectral Karyotyping/FISH technique.
29 Nov 2002 - Characterization of a small supernumerary marker chromosome as r(8) at prenatal diagnosis by MFISH.
30 Dec 2004 - Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.
29 Jun 2004 - Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis.
30 May 2004 - Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
29 Nov 2005
Related Article Map
Legend:
- FREE Full text Article.
- Abstract only.
- Title only. More help.
See a large map of 100+ related articles.