TY - JOUR
T1 - Identification of developmental endothelial locus-1 on circulating extracellular vesicles as a novel biomarker for early breast cancer detection
AU - Moon, Pyong Gon
AU - Lee, Jeong Eun
AU - Cho, Young Eun
AU - Lee, Soo Jung
AU - Jung, Jin Hyang
AU - Chae, Yee Soo
AU - Bae, Han Ik
AU - Kim, Young Bum
AU - Kim, In San
AU - Park, Ho Yong
AU - Baek, Moon Chang
N1 - Publisher Copyright:
© 2015 American Association for Cancer Research.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Purpose: Currently, there are no molecular biomarkers for the early detection of breast cancer. This study focused on identifying surface proteins found on circulating extracellular vesicles (EVs) for detecting early-stage breast cancer. Experimental Design: Circulating EVs, isolated from the plasma of 10 patients with breast cancer (stages I and II) and 5 healthy controls, were analyzed using LC-MS/MS. Developmental endothelial locus-1 protein (Del-1) was selected as a candidate biomarker. Two different ELISAswere used tomeasureDel-1 in plasma samples fromhealthy controls (n=81), patients with breast cancer (n=269), breast cancer patients after surgical resection (n=50), patients with benign breast tumors (n=64), and patients with noncancerous diseases (n=98) in two cohorts. Results: Plasma Del-1 levels were significantly higher (P < 0.0001) in patients with breast cancer than in all controls and returned to almost normal after tumor removal. The diagnostic accuracy of Del-1 was AUC, 0.961 [95% confidence interval (CI), 0.924-0.983], sensitivity of 94.70%, and specificity of 86.36% in test cohort and 0.968 (0.933-0.988), 92.31%, and 86.62% in validation cohort for early-stage breast cancer by one type of ELISA. Furthermore, Del-1 maintained diagnostic accuracy for patients with early-stage breast cancer using the other type of ELISA [0.946 (0.905-0.972), 90.90%, and 77.14% in the test cohort; 0.943 (0.900-0.971), 89.23%, and 80.99% in the validation cohort]. Conclusions: Del-1 on circulating EVs is a promising marker to improve identification of patients with early-stage breast cancer and distinguish breast cancer from benign breast tumors and noncancerous diseases.
AB - Purpose: Currently, there are no molecular biomarkers for the early detection of breast cancer. This study focused on identifying surface proteins found on circulating extracellular vesicles (EVs) for detecting early-stage breast cancer. Experimental Design: Circulating EVs, isolated from the plasma of 10 patients with breast cancer (stages I and II) and 5 healthy controls, were analyzed using LC-MS/MS. Developmental endothelial locus-1 protein (Del-1) was selected as a candidate biomarker. Two different ELISAswere used tomeasureDel-1 in plasma samples fromhealthy controls (n=81), patients with breast cancer (n=269), breast cancer patients after surgical resection (n=50), patients with benign breast tumors (n=64), and patients with noncancerous diseases (n=98) in two cohorts. Results: Plasma Del-1 levels were significantly higher (P < 0.0001) in patients with breast cancer than in all controls and returned to almost normal after tumor removal. The diagnostic accuracy of Del-1 was AUC, 0.961 [95% confidence interval (CI), 0.924-0.983], sensitivity of 94.70%, and specificity of 86.36% in test cohort and 0.968 (0.933-0.988), 92.31%, and 86.62% in validation cohort for early-stage breast cancer by one type of ELISA. Furthermore, Del-1 maintained diagnostic accuracy for patients with early-stage breast cancer using the other type of ELISA [0.946 (0.905-0.972), 90.90%, and 77.14% in the test cohort; 0.943 (0.900-0.971), 89.23%, and 80.99% in the validation cohort]. Conclusions: Del-1 on circulating EVs is a promising marker to improve identification of patients with early-stage breast cancer and distinguish breast cancer from benign breast tumors and noncancerous diseases.
UR - http://www.scopus.com/inward/record.url?scp=84964395591&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-15-0654
DO - 10.1158/1078-0432.CCR-15-0654
M3 - Article
C2 - 26603257
AN - SCOPUS:84964395591
SN - 1078-0432
VL - 22
SP - 1757
EP - 1766
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 7
ER -