TY - JOUR
T1 - Twist promotes tumor cell growth through YB-1 expression
AU - Shiota, Masaki
AU - Izumi, Hiroto
AU - Onitsuka, Takamitsu
AU - Miyamoto, Naoya
AU - Kashiwagi, Eiji
AU - Kidani, Akihiko
AU - Yokomizo, Akira
AU - Naito, Seiji
AU - Kohno, Kimitoshi
PY - 2008/1/1
Y1 - 2008/1/1
N2 - YB-1 controls gene expression through both transcriptional and translational mechanisms and is involved in various biological activities such as brain development, chemoresistance, and tumor progression. We have previously shown that YB-1 is overexpressed in cisplatin-resistant cells and is involved in resistance against DNA-damaging agents. Structural analysis of the YB-1 promoter reveals that several E-boxes may participate in the regulation of YB-1 expression. Here, we show that the E-box-binding transcription factor Twist is overexpressed in cisplatin-resistant cells and that YB-1 is a target gene of Twist. Silencing of either Twist or YB-1 expression induces G1 phase cell cycle arrest of tumor cell growth. Significantly, reexpression of YB-1 led to increase colony formation when Twist expression was down-regulated by small interfering RNA. However, cotransfection of Twist expression plasmid could not increase colony formation when YB-1 expression was down-regulated. Collectively, these data suggest that YB-1 is a major downstream target of Twist. Both YB-1 and Twist expression could induce tumor progression, promoting cell growth and driving oncogenesis in various cancers. Thus, both YB-1 and Twist may represent promising molecular targets for cancer therapy.
AB - YB-1 controls gene expression through both transcriptional and translational mechanisms and is involved in various biological activities such as brain development, chemoresistance, and tumor progression. We have previously shown that YB-1 is overexpressed in cisplatin-resistant cells and is involved in resistance against DNA-damaging agents. Structural analysis of the YB-1 promoter reveals that several E-boxes may participate in the regulation of YB-1 expression. Here, we show that the E-box-binding transcription factor Twist is overexpressed in cisplatin-resistant cells and that YB-1 is a target gene of Twist. Silencing of either Twist or YB-1 expression induces G1 phase cell cycle arrest of tumor cell growth. Significantly, reexpression of YB-1 led to increase colony formation when Twist expression was down-regulated by small interfering RNA. However, cotransfection of Twist expression plasmid could not increase colony formation when YB-1 expression was down-regulated. Collectively, these data suggest that YB-1 is a major downstream target of Twist. Both YB-1 and Twist expression could induce tumor progression, promoting cell growth and driving oncogenesis in various cancers. Thus, both YB-1 and Twist may represent promising molecular targets for cancer therapy.
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UR - http://www.scopus.com/inward/citedby.url?scp=39149103407&partnerID=8YFLogxK
U2 - 10.1158/0008-5472.CAN-07-2981
DO - 10.1158/0008-5472.CAN-07-2981
M3 - Article
C2 - 18172301
AN - SCOPUS:39149103407
SN - 0008-5472
VL - 68
SP - 98
EP - 105
JO - Cancer Research
JF - Cancer Research
IS - 1
ER -