Bazooka inhibitors, broadly speaking, involve chemicals that can interrupt the processes of cell polarity and cytoskeletal organization. Colchicine, Nocodazole, Taxol, and Vinblastine all disrupt microtubule dynamics, which are essential for cell polarity and can indirectly affect the function of Bazooka, a key player in establishing cell polarity.
Cytochalasin D, Latrunculin B, and Jasplakinolide all affect actin dynamics, another crucial component of the cytoskeleton. By altering actin polymerization, these chemicals can indirectly affect Bazooka. Blebbistatin, Y-27632, Forskolin, Brefeldin A, and Tunicamycin all interfere with different cellular processes that can indirectly affect the function of Bazooka. Blebbistatin inhibits myosin II, Y-27632 inhibits ROCK, Forskolin alters cAMP levels, Brefeldin A disrupts protein transport, and Tunicamycin inhibits N-linked glycosylation. All these processes can influence cell polarity and, hence, can affect Bazooka.