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Differential expression of the LGI and SLIT families of genes in human cancer cells

  • Michael R. Rossi
    ,
  • Kristin Huntoon
    ,
  • John K. Cowell(corresponding author)
*Corresponding author for this work
  • Roswell Park Cancer Institute
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

The LGI and SLIT genes have a distinctive leucine-rich repeat motif in the N-terminal end of the protein which is indicative of either receptor function or an interaction with the extracellular matrix. Members of the LGI and SLIT family of genes have been implicated in specific cancers and have been suggested to have a restricted pattern of expression in normal cells. To investigate the extent and distribution of the expression of these genes in cancer cells we have analyzed their expression levels in a range of tumor cell types. Different tumor types appear to hold a preference for the specific members of the families which are expressed. Differential expression between cell lines, from the same tumor type, implies a role for inactivation and reactivation of these genes during tumorigenesis. The detailed characterization of the expression pattern in these tumor cells offers the opportunity to perform a functional analysis of these individual genes.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 85-90 (6 pages)

Journal (Volume, Issue Number)

Gene (Volume 356, Issue 1-2)

Publication milestones

  • Published - 08/15/2005

Publication status

Published - 08/15/2005

ISSN

0378-1119

Publication IDs

  • Scopus: 23844472049
  • PubMed: 16000246

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
0.23
SciVal
Author count
3
SciVal
citations
22
SciVal
Paper percentile
74
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
22
Citation count
25

Funding Details

This work was supported by grant NSO46706 from the National Institute of Neurological Disorders and Stroke, and in part by the National Cancer Institute Roswell Park Cancer Center Support Grant CA 16056.
FundersFunding number
NCI
P30CA016056
NINDS
-