p21CIP1/WAF1 is a downstream effector of tumor suppressors and functions as a cyclin-dependent kinase inhibitor to block cellular proliferation. Breast tumors may derive from self-renewing tumorinitiating cells (BT-ICs), which contribute to tumor progression, recurrence, and therapy resistance. The role of p21CIP1 in regulating features of tumor stem cells in vivo is unknown. Herein, deletion of p21CIP1, which enhanced the rate of tumorigenesis induced by mammary-targeted Ha-Ras or c-Myc, enhanced gene expression profiles and immunohistochemical features of epithelial mesenchymal transition (EMT) and putative cancer stem cells in vivo. Silencing of p21CIP1 enhanced, and expression of p21CIP1 repressed, features of EMT in transformed immortal human MEC lines. p21CIP1 attenuated oncogene-induced BT-IC and mammosphere formation. Thus, the in vitro cell culture assays reflect the changes observed in vivo in transgenic mice. These findings establish a link between the loss of p21CIP1 and the acquisition of breast cancer EMT and stem cell properties in vivo.
p21CIP1 attenuates Ras- and c-Myc-dependent breast tumor epithelial mesenchymal transition and cancer stem cell-like gene expression in vivo / M., Liu; M. C., Casimiro; C., Wang; L. A., Shirley; X., Jiao; S., Katiyar; X., Ju; Z., Li; Z., Yu; J., Zhou; M., Johnson; Fortina, Paolo; T., Hyslop; J. J., Windle; R. G., Pestell. - In: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. - ISSN 1091-6490. - STAMPA. - 106:45(2009), pp. 19035-19039. [10.1073/pnas.0910009106]
p21CIP1 attenuates Ras- and c-Myc-dependent breast tumor epithelial mesenchymal transition and cancer stem cell-like gene expression in vivo.
FORTINA, PAOLO;
2009
Abstract
p21CIP1/WAF1 is a downstream effector of tumor suppressors and functions as a cyclin-dependent kinase inhibitor to block cellular proliferation. Breast tumors may derive from self-renewing tumorinitiating cells (BT-ICs), which contribute to tumor progression, recurrence, and therapy resistance. The role of p21CIP1 in regulating features of tumor stem cells in vivo is unknown. Herein, deletion of p21CIP1, which enhanced the rate of tumorigenesis induced by mammary-targeted Ha-Ras or c-Myc, enhanced gene expression profiles and immunohistochemical features of epithelial mesenchymal transition (EMT) and putative cancer stem cells in vivo. Silencing of p21CIP1 enhanced, and expression of p21CIP1 repressed, features of EMT in transformed immortal human MEC lines. p21CIP1 attenuated oncogene-induced BT-IC and mammosphere formation. Thus, the in vitro cell culture assays reflect the changes observed in vivo in transgenic mice. These findings establish a link between the loss of p21CIP1 and the acquisition of breast cancer EMT and stem cell properties in vivo.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
