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Cloning of TACC1, an embryonically expressed, potentially transforming coiled coil containing gene, from the 8p11 breast cancer amplicon

  • Ivan H. Still(corresponding author)
    ,
  • Mark Hamilton
    ,
  • Pauline Vince
    ,
  • Alan Wolfman
    ,
*Corresponding author for this work
  • Cleveland Clinic Foundation
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Amplification of several chromosomal regions have been observed in human breast carcinomas. One such region, 8p11, is amplified in 10-15% of tumor samples. Although the FGFR1 gene is located close to this region, and is often included within the amplicon, the observation that tumors exhibiting 8p11 amplification do not always overexpress FGFR1 suggests that another gene located close to FGFR1 is involved in the tumorigenic process. We now report the precise location of four expressed sequence tags (ESTs) within this region and the cloning of a novel gene, designated TACC1 (transforming acidic coiled coil gene 1), which encodes an 8 kb transcript and which is expressed at high levels during early embryogenesis. Constitutive expression of this gene under the control of the cytomegalovirus (CMV) promoter in mouse fibroblasts, results in cellular transformation and anchorage independent growth, suggesting that inappropriate expression can impart a proliferative advantage. This observation raises the possibility that amplification of TACC1 could promote malignant growth, thereby making TACC1 an attractive candidate for the gene promoting tumorigenicity as a result of the 8p11 amplification in human breast cancers.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 4032-4038 (7 pages)

Journal (Volume, Issue Number)

Oncogene (Volume 18, Issue 27)

Publication milestones

  • Published - 07/08/1999

Publication status

Published - 07/08/1999

ISSN

0950-9232

Publication IDs

  • Scopus: 0033536197
  • PubMed: 10435627

Publication metrics

Metrics

SciVal
citations
100
SciVal
FWCI
1.78
SciVal
Author count
5
SciVal
Paper percentile
93
SciVal
Top percentile
10
Fractional count
1
Fractional count
0.20
Fractional count
4
Fractional count
0.80
Fractional count
1
Fractional count
1
Scopus
citations

PlumX, opens in new tab

Citation count
99
Captures
16
Mentions
3

Funding Details

The first two authors contributed equally to this report. This work is in part supported by NIH grant GM49652 and AHA grant 96001110 to Alan Wolfman.
FundersFunding numbers
NIH
-
NIGMS
R01GM049652
AHA
96001110