TY - JOUR
T1 - Expression of WISPs and of their novel alternative variants in human hepatocellular carcinoma cells
AU - D'Alessandro, Natale
AU - Labbozzetta, Manuela
AU - Montalto, Giuseppe
AU - Giannitrapani, Lydia
AU - Notarbartolo Di Villarosa, Monica
AU - Cervello, Melchiorre
AU - Azzolina, Antonina
AU - Lampiasi, Nadia
PY - 2004
Y1 - 2004
N2 - 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.
AB - 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.
KW - CCN
KW - WISP
KW - Wnt
KW - alternative splicing
KW - hepatocellular carcinoma
KW - CCN
KW - WISP
KW - Wnt
KW - alternative splicing
KW - hepatocellular carcinoma
UR - http://hdl.handle.net/10447/10772
M3 - Article
SN - 0077-8923
VL - 1028
SP - 432
EP - 439
JO - Annals of the New York Academy of Sciences
JF - Annals of the New York Academy of Sciences
ER -