TY - JOUR
T1 - Bone morphogenetic protein-7 inhibits telomerase activity, telomere maintenance, and cervical tumor growth
AU - Cassar, Lucy
AU - Li, He
AU - Pinto, Ruvantha
AU - Nicholls, Craig
AU - Bayne, Sharyn
AU - Liu, Jun-Ping
PY - 2008
Y1 - 2008
N2 - Telomere maintenance is critical in tumor cell immortalization. Here, we report that the cytokine bone morphogenetic protein-7 (BMP7) inhibits telomerase activity that is required for telomere maintenance in cervical cancer cells. Application of human recombinant BMP7 triggers a repression of the human telomerase reverse transcriptase (hTERT) gene, shortening of telomeres, and hTERT repressiona??dependent cervical cancer cell death. Continuous treatment of mouse xenograft tumors with BMP7, or silencing the hTERT gene, results in sustained inhibition of telomerase activity, shortening of telomeres, and tumor growth arrest. Overexpression of hTERT lengthens telomeres and blocks BMP7-induced tumor growth arrest. Thus, BMP7 negatively regulates telomere maintenance, inducing cervical tumor growth arrest by a mechanism of inducing hTERT gene repression.
AB - Telomere maintenance is critical in tumor cell immortalization. Here, we report that the cytokine bone morphogenetic protein-7 (BMP7) inhibits telomerase activity that is required for telomere maintenance in cervical cancer cells. Application of human recombinant BMP7 triggers a repression of the human telomerase reverse transcriptase (hTERT) gene, shortening of telomeres, and hTERT repressiona??dependent cervical cancer cell death. Continuous treatment of mouse xenograft tumors with BMP7, or silencing the hTERT gene, results in sustained inhibition of telomerase activity, shortening of telomeres, and tumor growth arrest. Overexpression of hTERT lengthens telomeres and blocks BMP7-induced tumor growth arrest. Thus, BMP7 negatively regulates telomere maintenance, inducing cervical tumor growth arrest by a mechanism of inducing hTERT gene repression.
UR - http://cancerres.aacrjournals.org/content/68/22/9157.full.pdf+html
U2 - 10.1158/0008-5472.CAN-08-1323
DO - 10.1158/0008-5472.CAN-08-1323
M3 - Article
SN - 0008-5472
VL - 68
SP - 9157
EP - 9166
JO - Cancer Research
JF - Cancer Research
IS - 22
ER -