Insulin and novel thioglycosides exert suppressive effect on human breast and colon carcinoma cells
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Siddarth Agrawal1, Marta Wozniak1, Mateusz Luc1, Kinga Walaszek1, Ewa Pielka1, Wieslaw Szeja2, Gabriela Pastuch-Gawolek2,3, Andrzej Gamian4 and Piotr Ziolkowski1
1Department of Pathology, Wroclaw Medical University, Wroclaw, Poland
2Department of Organic Chemistry, Bioorganic Chemistry and Biotechnology, Silesian University of Technology, Gliwice, Poland
3Biotechnology Centre, Silesian University of Technology, Gliwice, Poland
4Department of Biochemistry, Wroclaw Medical University, Wroclaw, Poland
Siddarth Agrawal, email: email@example.com
Keywords: cancer therapy; thioglycosides; insulin; breast cancer; colon cancer
Received: September 05, 2017 Accepted: November 16, 2017 Published: December 11, 2017
The rationale for the implementation of novel therapies should be based on hallmarks of cancer. Two novel compounds labelled as thioglycoside A and B were designed and evaluated on breast and colon cancer cell lines. We assessed their cytotoxic effect after sensitizing cancer cells with insulin. In order to explore the underlying mechanisms, we performed tests to assess cell migration and motility, apoptosis, expression of glucose transporter 1 and proapoptotic proteins. Both compounds proved to have an antitumor effect which was significantly enhanced in combination with insulin. Linking glucose and anticancer agent presents an approach that exploits the Warburg effect. Targeting dysfunctional glycometabolism and increased glucose absorption is emerging as a promising anticancer strategy.
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