TY - JOUR
T1 - Galectin-3 inhibition suppresses drug resistance, motility, invasion and angiogenic potential in ovarian cancer
AU - Mirandola, Leonardo
AU - Yu, Yuefei
AU - Cannon, Martin J.
AU - Jenkins, Marjorie R.
AU - Rahman, Rakhshanda L.
AU - Nguyen, Diane D.
AU - Grizzi, Fabio
AU - Cobos, Everardo
AU - Figueroa, Jose A.
AU - Chiriva-Internati, Maurizio
N1 - Publisher Copyright:
© 2014 Elsevier Inc. All rights reserved.
PY - 2014/12/1
Y1 - 2014/12/1
N2 - Objective. Ovarian cancer is the most deadly gynecologic malignancy worldwide. Since the pathogenesis of ovarian cancer is incompletely understood, and there are no available screening techniques for early detection, most patients are diagnosed with advanced, incurable disease. In an effort to develop innovative and effective therapies for ovarian cancer, we tested the effectiveness of Galecti-3C in vitro. This is a truncated, dominant negative form of Galectin-3, which is thought to act by blocking endogenous Galectin-3. Methods. We produced a truncated, dominant-negative form of Galectin-3, namely Galetic-3C. Ovarian cancer cell lines and primary cells from ovarian cancer patients were treated with Galectin-3C, and growth, drug sensitivity, and angiogenesis were tested. Result. We show, for the first time, that Galectin-3C significantly reduces the growth, motility, invasion, and angiogenic potential of cultured OC cell lines and primary cells established from OC patients. Conclusions. Our findings indicate that Galectin-3C is a promising new compound for the treatment of ovarian cancer.
AB - Objective. Ovarian cancer is the most deadly gynecologic malignancy worldwide. Since the pathogenesis of ovarian cancer is incompletely understood, and there are no available screening techniques for early detection, most patients are diagnosed with advanced, incurable disease. In an effort to develop innovative and effective therapies for ovarian cancer, we tested the effectiveness of Galecti-3C in vitro. This is a truncated, dominant negative form of Galectin-3, which is thought to act by blocking endogenous Galectin-3. Methods. We produced a truncated, dominant-negative form of Galectin-3, namely Galetic-3C. Ovarian cancer cell lines and primary cells from ovarian cancer patients were treated with Galectin-3C, and growth, drug sensitivity, and angiogenesis were tested. Result. We show, for the first time, that Galectin-3C significantly reduces the growth, motility, invasion, and angiogenic potential of cultured OC cell lines and primary cells established from OC patients. Conclusions. Our findings indicate that Galectin-3C is a promising new compound for the treatment of ovarian cancer.
KW - Angiogenesis
KW - Galectin-3
KW - Galectin-3C
KW - Invasion
KW - Ovarian cancer
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U2 - 10.1016/j.ygyno.2014.09.021
DO - 10.1016/j.ygyno.2014.09.021
M3 - Article
C2 - 25284038
AN - SCOPUS:84920834833
SN - 0090-8258
VL - 135
SP - 573
EP - 579
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 3
ER -