Volume 1028, Issue 1 p. 432-439

Expression of WISPs and of Their Novel Alternative Variants in Human Hepatocellular Carcinoma Cells

MELCHIORRE CERVELLO

Corresponding Author

MELCHIORRE CERVELLO

Istituto di Biomedicina e Immunologia Molecolare, CNR, Palermo, Italy

Address for correspondence: Dr. Melchiorre Cervello, Istituto di Biomedicina e Immunologia Molecolare, CNR, Via Ugo La Malfa 153, 90146 Palermo, Italy. Voice: +39 091-6809-534; fax: +39 091-6809-548. [email protected]Search for more papers by this author
LYDIA GIANNITRAPANI

LYDIA GIANNITRAPANI

Dipartimento di Clinica Medica e Patologie Emergenti, Università di Palermo, Palermo, Italy

Search for more papers by this author
MANUELA LABBOZZETTA

MANUELA LABBOZZETTA

Dipartimento di Clinica Medica e Patologie Emergenti, Università di Palermo, Palermo, Italy

Search for more papers by this author
MONICA NOTARBARTOLO

MONICA NOTARBARTOLO

Dipartimento di Scienze Farmacologiche, Università di Palermo, Palermo, Italy

Search for more papers by this author
NATALE D'ALESSANDRO

NATALE D'ALESSANDRO

Dipartimento di Scienze Farmacologiche, Università di Palermo, Palermo, Italy

Search for more papers by this author
NADIA LAMPIASI

NADIA LAMPIASI

Istituto di Biomedicina e Immunologia Molecolare, CNR, Palermo, Italy

Search for more papers by this author
ANTONINA AZZOLINA

ANTONINA AZZOLINA

Istituto di Biomedicina e Immunologia Molecolare, CNR, Palermo, Italy

Search for more papers by this author
GIUSEPPE MONTALTO

GIUSEPPE MONTALTO

Dipartimento di Clinica Medica e Patologie Emergenti, Università di Palermo, Palermo, Italy

Search for more papers by this author
First published: 12 January 2006
Citations: 36

Abstract

Abstract: WISPs (Wnt-induced secreted proteins) are members of the CCN (CTGF/Cyr61/Nov) family involved in fibrotic disorders and tumorigenesis. They have a typical structure composed of four conserved cysteine-rich modular domains, but variants of CCN members lacking one or more modules, generated by alternative splicing or gene mutations, have been described in various pathological conditions. WISP genes were first described as downstream targets of the Wnt signaling pathway, which is frequently altered in human hepatocellular carcinoma (HCC). In the present study, WISP mRNA expression was analyzed by RT-PCR in four human HCC cell lines (HepG2, HuH-6, HuH-7, HA22T/VGH). Our results show for the first time that WISP1, WISP1v, and WISP3 are expressed in HCC cell lines. Moreover, we identified two novel variants, generated by alternative splicing of WISP1 and WISP3, respectively, named WISP1Δex3-4 and WISP3vL. Overall, our study suggests that WISP transcripts may have a role in the development of HCC, although further studies are necessary to clarify the relative importance of the expression of wild-type WISPs, as well as of their novel variants, in this tumor type.