TY - JOUR
T1 - PSF1, a DNA replication factor expressed widely in stem and progenitor cells, drives tumorigenic and metastatic properties
AU - Nagahama, Yumi
AU - Ueno, Masaya
AU - Miyamoto, Satoru
AU - Morii, Eiichi
AU - Minami, Takashi
AU - Mochizuki, Naoki
AU - Saya, Hideyuki
AU - Takakura, Nobuyuki
PY - 2010/2/1
Y1 - 2010/2/1
N2 - PSF1 (partner of sld five 1) is an evolutionarily conserved DNA replication factor implicated in DNA replication in lower species that is strongly expressed in a wide range of normal stem cell populations and progenitor cell populations. Because stem and progenitor cells possess high proliferative capacity, we hypothesized that PSF1 may play an important role in tumor growth. To begin to investigate PSF1 function in cancer cells, we cloned the mouse PSF1 promoter and generated lung and colon carcinoma cells that stably express a PSF1 promoter-reporter gene. Reporter expression in cells correlated with endogenous PSF1 mRNA expression. In a tumor cell xenograft model, high levels of reporter expression correlated with high proliferative activity, serial transplantation potential, and metastatic capability. Notably, cancer cells expressing reporter levels localized to perivascular regions in tumors and displayed expression signatures related to embryonic stem cells. RNAi-mediated silencing of endogenous PSF1 inhibited cancer cell growth by disrupting DNA synthesis and chromosomal segregation. These findings implicate PSF1 in tumorigenesis and offer initial evidence of its potential as a theranostic target.
AB - PSF1 (partner of sld five 1) is an evolutionarily conserved DNA replication factor implicated in DNA replication in lower species that is strongly expressed in a wide range of normal stem cell populations and progenitor cell populations. Because stem and progenitor cells possess high proliferative capacity, we hypothesized that PSF1 may play an important role in tumor growth. To begin to investigate PSF1 function in cancer cells, we cloned the mouse PSF1 promoter and generated lung and colon carcinoma cells that stably express a PSF1 promoter-reporter gene. Reporter expression in cells correlated with endogenous PSF1 mRNA expression. In a tumor cell xenograft model, high levels of reporter expression correlated with high proliferative activity, serial transplantation potential, and metastatic capability. Notably, cancer cells expressing reporter levels localized to perivascular regions in tumors and displayed expression signatures related to embryonic stem cells. RNAi-mediated silencing of endogenous PSF1 inhibited cancer cell growth by disrupting DNA synthesis and chromosomal segregation. These findings implicate PSF1 in tumorigenesis and offer initial evidence of its potential as a theranostic target.
UR - http://www.scopus.com/inward/record.url?scp=76249095216&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=76249095216&partnerID=8YFLogxK
U2 - 10.1158/0008-5472.CAN-09-3662
DO - 10.1158/0008-5472.CAN-09-3662
M3 - Article
C2 - 20103637
AN - SCOPUS:76249095216
SN - 0008-5472
VL - 70
SP - 1215
EP - 1224
JO - Cancer Research
JF - Cancer Research
IS - 3
ER -