The predominant CD44 splice variant in prostate cancer binds fibronectin, and calcitonin stimulates its expression.

Abstract

BACKGROUND:

Prostate cancer (PC) consistently overexpresses variant the (v) isoform of the cell adhesion protein CD44, and loses expression of the standard (s) isoform.

MATERIALS AND METHODS:

We re-expressed CD44 full-length (exons 1-20) or standard (exons 1-5 + 16-20) or enforced stable RNAi against CD44v, and the examined functional effects on PC. The effect of stable knockout of calcitonin, a paracrine factor, or its receptor, on CD44 was assessed.

RESULTS:

Re-expression of full-length CD44 or CD44s increased the total CD44 mRNA and CD44s protein while suppressing CD44v. These approaches, and RNAi to CD44v, decreased invasion. In adhesion assays, benign prostate cells bound mainly to hyaluronan, whereas PC lost affinity for hyaluronan but bound more strongly to fibronectin. Re-expressing CD44s restored predominant hyaluronan binding. Knockout of the calcitonin receptor in PC-3 derived cells caused marked loss of CD44v expression and reversion to CD44s expression.

CONCLUSION:

Calcitonin influenced PC's balance between CD44s and CD44v. CD44v controlled invasiveness, altered ligand binding, and provides a target for therapeutic intervention.

• Authors: Kenneth A Iczkowski, A Levi Omara-Opyene, Girish V Shah
• Journal: Anticancer research (Anticancer Res) 2006 Jul-Aug Vol. 26 Issue 4B Pg. 2863-72 ISSN: 0250-7005 [Print] Greece
• PMID: 16886606 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)

Chemical References

• CD44 protein, human
• Fibronectins
• Hyaluronan Receptors
• Protein Isoforms
• RNA, Messenger
• RNA, Small Interfering
• Receptors, Calcitonin
• Calcitonin

Topics

• Alternative Splicing
• Calcitonin (deficiency, genetics, metabolism)
• Cell Adhesion (physiology)
• Cell Line, Tumor
• Fibronectins (metabolism)
• Gene Silencing
• Humans
• Hyaluronan Receptors (biosynthesis, genetics, metabolism)
• Male
• Prostatic Neoplasms (genetics, metabolism, pathology)
• Protein Isoforms
• RNA, Messenger (biosynthesis, genetics)
• RNA, Small Interfering (genetics)
• Receptors, Calcitonin (deficiency, genetics)