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PMID: 7529235 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

New CD44 splice variants associated with human breast cancers.

Journal of cellular physiology ·Vol. 162 ·No. 1 ·1995-01-00 ·Pages 127-33

Iida N, Bourguignon LY

Abstract

Changes in the CD44 variant (CD44v) isoforms on the cell surface have been correlated with tumor metastasis. In this study we have examined the expression of CD44 variant isoforms in human breast carcinoma samples by a variety of techniques including immunohistochemistry, reverse transcriptase-polymerase chain reaction (RT-PCR), and nucleotide sequencing. Using RT-PCR, we have determined that normal human breast tissue contains primarily the CD44 epithelial (CD44E) form and very little CD44 standard (CD44s) form. However, metastatic breast carcinomas appear to overexpress both the CD44E and CD44s forms and also display multiple new species of CD44 variant isoforms. Histocytochemical staining using anti-CD44 antibody (recognizing a common determinant of the CD44 class of glycoproteins) confirms that the CD44 molecules are overexpressed and preferentially located in metastatic breast cancer tissues. Nucleotide sequencing analyses indicate that at least four new CD44 variant isoforms (i.e., displaying unique splicing via the insertion or the deletion of exons 7, 10, 11, and 14) may be closely associated with human metastatic breast cancers. These newly described CD44 variant isoforms may be useful for monitoring the progression of human breast cancer metastasis.

MeSH Terms
Base Sequence Breast Neoplasms/genetics,immunology,pathology Carrier Proteins/analysis,genetics DNA, Neoplasm/analysis,genetics Gene Expression Regulation, Neoplastic Genetic Variation Humans Hyaluronan Receptors Immunohistochemistry Isomerism Molecular Sequence Data Polymerase Chain Reaction Receptors, Cell Surface/analysis,genetics Receptors, Lymphocyte Homing/analysis,genetics
Chemicals
Carrier Proteins DNA, Neoplasm Hyaluronan Receptors Receptors, Cell Surface Receptors, Lymphocyte Homing
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Iida N
Department of Cell Biology and Anatomy, School of Medicine, University of Miami, Florida 33101.
Bourguignon L Y
Article Info
Journal
Journal of cellular physiology
Abbr.
J Cell Physiol
ISSN
0021-9541
Published
1995-01-00
Pages
127-33
Language
English
Region
United States
NLM ID
0050222
Subset
IM
Grants
NIGMS NIH HHS · GM 36353 · United States
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