HMGA1 is a member of a small family of architectural transcription factors involved in the coordinate assembly of multiprotein complexes referred to as enhanceosomes. In addition to their role in cell proliferation, differentiation, and development, high-mobility group proteins of the A type ( HMGA) family members behave as transforming protoncogenes either in vitro or in animal models. Recent reports indicated that HMGA1 might counteract p53 pathway and provided an interesting hint on the mechanisms determining HMGA's transforming potential. HMGA1 expression is deregulated in a very large array of human tumors, including cervical cancer, but very limited information is available on the molecular mechanisms leading to HMGA1 deregulation in cancer cells. Here, we report that HMGA1 expression is sustained by human papilloma virus (HPV) E6/E7 proteins in cervical cancer, as demonstrated by either E6/E7 overexpression or by repression through RNA interference. Knocking down HMGA1 expression by means of RNA interference, we also showed that it is involved in cell proliferation and contributes to p53 inactivation in this type of neoplasia. Finally, we show that HMGA1 is necessary for the full expression of HPV18 E6 and E7 oncoproteins thus establishing a positive autoregulatory loop between HPV E6/E7 and HMGA1 expression.

Human papilloma virus-dependent HMGA1 expression is a relevant step in cervical carcinogenesis / M., Mellone; C., Rinaldi; Massimi, Isabella; Petroni, Marialaura; Veschi, Veronica; Talora, Claudio; S., Truffa; Stabile, MARIA HELENA; Frati, Luigi; Screpanti, Isabella; Gulino, Alberto; Giannini, Giuseppe. - In: NEOPLASIA. - ISSN 1522-8002. - STAMPA. - 10:8(2008), pp. 773-781. [10.1593/neo.08462]

Human papilloma virus-dependent HMGA1 expression is a relevant step in cervical carcinogenesis

MASSIMI, ISABELLA;PETRONI, MARIALAURA;VESCHI, VERONICA;TALORA, Claudio;STABILE, MARIA HELENA;FRATI, Luigi;SCREPANTI, Isabella;GULINO, Alberto;GIANNINI, Giuseppe
2008

Abstract

HMGA1 is a member of a small family of architectural transcription factors involved in the coordinate assembly of multiprotein complexes referred to as enhanceosomes. In addition to their role in cell proliferation, differentiation, and development, high-mobility group proteins of the A type ( HMGA) family members behave as transforming protoncogenes either in vitro or in animal models. Recent reports indicated that HMGA1 might counteract p53 pathway and provided an interesting hint on the mechanisms determining HMGA's transforming potential. HMGA1 expression is deregulated in a very large array of human tumors, including cervical cancer, but very limited information is available on the molecular mechanisms leading to HMGA1 deregulation in cancer cells. Here, we report that HMGA1 expression is sustained by human papilloma virus (HPV) E6/E7 proteins in cervical cancer, as demonstrated by either E6/E7 overexpression or by repression through RNA interference. Knocking down HMGA1 expression by means of RNA interference, we also showed that it is involved in cell proliferation and contributes to p53 inactivation in this type of neoplasia. Finally, we show that HMGA1 is necessary for the full expression of HPV18 E6 and E7 oncoproteins thus establishing a positive autoregulatory loop between HPV E6/E7 and HMGA1 expression.
2008
01 Pubblicazione su rivista::01a Articolo in rivista
Human papilloma virus-dependent HMGA1 expression is a relevant step in cervical carcinogenesis / M., Mellone; C., Rinaldi; Massimi, Isabella; Petroni, Marialaura; Veschi, Veronica; Talora, Claudio; S., Truffa; Stabile, MARIA HELENA; Frati, Luigi; Screpanti, Isabella; Gulino, Alberto; Giannini, Giuseppe. - In: NEOPLASIA. - ISSN 1522-8002. - STAMPA. - 10:8(2008), pp. 773-781. [10.1593/neo.08462]
File allegati a questo prodotto
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/364773
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 8
  • Scopus 17
  • ???jsp.display-item.citation.isi??? 14
social impact