In Silico Modeling-based Identification of GLUT4 Selective Inhibitors for Cancer Therapy [Protein Structure and Folding]

April 6th, 2015 by Mishra, R. K., Wei, C., Hresko, R. C., Bajpai, R., Heitmeier, M., Matulis, S. M., Nooka, A. K., Rosen, S. T., Hruz, P. W., Schiltz, G. E., Shanmugam, M.

Tumor cells rely on elevated glucose consumption and metabolism for survival and proliferation. Glucose transporters mediating glucose entry are key proximal rate-limiting checkpoints (1). Unlike GLUT1 that is highly expressed in cancer and more ubiquitously expressed in normal tissues (2), GLUT4 exhibits more limited normal expression profiles. We have previously determined that insulin responsive GLUT4 is constitutively localized on the plasma membrane of myeloma cells (3). Consequently, suppression of GLUT4 or inhibition of glucose transport with the HIV protease inhibitor ritonavir elicited growth arrest and/or apoptosis in multiple myeloma (3). GLUT4 inhibition also caused sensitization to metformin in multiple myeloma and chronic lymphocytic leukemia (CLL) and a number of solid tumors suggesting the broader therapeutic utility of targeting GLUT4 (4,5). Our current study sought to identify selective inhibitors of GLUT4 to develop a more potent cancer chemotherapeutic with fewer potential off-target effects. Recently, the crystal structure of GLUT1 in an inward open conformation was reported (6). While this is an important achievement, a full understanding of the structural biology of facilitative glucose transport remains elusive. To date, there is no three dimensional structure for GLUT4. We have generated a homology model for GLUT4 that we utilized to screen for drug-like compounds from a library of eighteen million compounds. Despite 68% homology (7) between GLUT1 and GLUT4, our virtual screen identified two potent compounds that were shown to target GLUT4 preferentially over GLUT1 and block glucose transport. Our results strongly bolster the utility of developing GLUT4 selective inhibitors as anti-cancer therapeutics.