TY - JOUR
T1 - Extended use of intravenous bisphosphonate therapy for the prevention of skeletal complications in patients with cancer
AU - Wang, Xi
AU - Ni, Jing
AU - Hsu, Chen Long
AU - Johnykutty, Sharlin
AU - Tang, Ping
AU - Ho, Yuan Soon
AU - Lee, Chia Hwa
AU - Yeh, Shuyuang
PY - 2009/11/13
Y1 - 2009/11/13
N2 - We show that TAP/Sec14L2 had a high expression in normal/benign breast, prostate, and liver tissues as compared to lung, colon, and kidney. Its expression was downregulated in breast cancer cell lines shown by quantitative-PCR. Further, 57% of 141 human invasive breast carcinomas had no or markedly reduced TAP/Sec14L2 expression by immunohistochemical staining, and the rate increased to 80% in high grade invasive carcinomas ( p <.01). This downregulation of TAP/Sec14L2 was also present in ductal carcinoma in situ(DCIS) associated with invasive carcinomas. These findings raise the possibility that TAP/Sec14L2 may serve as a tumor suppressor in breast carcinogenesis.
AB - We show that TAP/Sec14L2 had a high expression in normal/benign breast, prostate, and liver tissues as compared to lung, colon, and kidney. Its expression was downregulated in breast cancer cell lines shown by quantitative-PCR. Further, 57% of 141 human invasive breast carcinomas had no or markedly reduced TAP/Sec14L2 expression by immunohistochemical staining, and the rate increased to 80% in high grade invasive carcinomas ( p <.01). This downregulation of TAP/Sec14L2 was also present in ductal carcinoma in situ(DCIS) associated with invasive carcinomas. These findings raise the possibility that TAP/Sec14L2 may serve as a tumor suppressor in breast carcinogenesis.
KW - BCa
KW - TAP
UR - http://www.scopus.com/inward/record.url?scp=70450212895&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=70450212895&partnerID=8YFLogxK
U2 - 10.3109/07357900802392659
DO - 10.3109/07357900802392659
M3 - Article
AN - SCOPUS:70450212895
SN - 0735-7907
VL - 27
SP - 971
EP - 977
JO - Cancer Investigation
JF - Cancer Investigation
IS - 10
ER -