1997
DOI: 10.1038/sj.onc.1201065
|View full text |Cite
|
Sign up to set email alerts
|

A putative serine/threonine kinase encoding gene BTAK on chromosome 20q13 is amplified and overexpressed in human breast cancer cell lines

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

9
344
1
3

Year Published

1998
1998
2003
2003

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 433 publications
(357 citation statements)
references
References 15 publications
9
344
1
3
Order By: Relevance
“…Fourthly, stable downregulation of Aurora2/BTAK/STK15 after antisense transfection affects cell survival in vitro and in vivo through a change in the distribution of cell cycle phases. These results seem compatible with the fact that Aurora2/ BTAK/STK15 was originally isolated in centrosomes and the mitotic spindle (Sen et al, 1997). It has been thought that deregulated duplication and distribution of centrosomes might be implicated in the chromosome segregation abnormalities seen in many types of malignant cells.…”
Section: Discussionsupporting
confidence: 86%
See 2 more Smart Citations
“…Fourthly, stable downregulation of Aurora2/BTAK/STK15 after antisense transfection affects cell survival in vitro and in vivo through a change in the distribution of cell cycle phases. These results seem compatible with the fact that Aurora2/ BTAK/STK15 was originally isolated in centrosomes and the mitotic spindle (Sen et al, 1997). It has been thought that deregulated duplication and distribution of centrosomes might be implicated in the chromosome segregation abnormalities seen in many types of malignant cells.…”
Section: Discussionsupporting
confidence: 86%
“…This result indicated that Aurora2/BTAK/STK15 may be involved in the cell proliferation of B-cell NHL. As Aurora2/BTAK/STK15 is essential for centrosomes and the mitotic spindle (Sen et al, 1997) and is weakly expressed in normal tissues, we attempted to treat normal fibroblasts with the antisense oligo of Aurora2/BTAK/STK15 and analysed the effect for cell proliferation incorporating [ 3 H] TdR (data not shown). However, there was no downregulation of DNA synthesis in normal fibroblasts even at a high concentration of 10 lmol/l of Aurora2/BTAK/STK15 antisense treatment.…”
Section: Inhibition Of Cell Growth By An Antisense Oligonucleotide Onmentioning
confidence: 99%
See 1 more Smart Citation
“…Several studies indicate that Aurora-A has a close link to cancer pathogenesis [64][65][66][67][68]. The Aurora-A gene was mapped to chromosome 20q13.2-13.3, a region often amplified in human cancers [69].…”
Section: Aurora and Cancermentioning
confidence: 99%
“…The Aurora-A gene was mapped to chromosome 20q13.2-13.3, a region often amplified in human cancers [69]. In addition, it has been re-ported that the level of Aurora-A mRNA is high in colon cancer [64,65], as well as in cell lines derived from breast, ovarian, colon, prostate, neuroblastoma and cervical cancers [66]. Ectopic expression of Aurora-A in mouse NIH3T3 cells display the phenotype of abnormal centrosomes replication and cell transformation.…”
Section: Aurora and Cancermentioning
confidence: 99%