Liquid-crystalline (LC) hybrid polymers with functionalized silsesquioxanes with various proportions of LC monomer were synthesized by the reaction of polyhedral oligomeric silsesquioxane (POSS) macromonomer with methacrylate monomer having an LC moiety under common free-radical conditions. The obtained LC hybrid polymers were soluble in common solvents such as tetrahydrofuran, toluene, and chloroform, and their structures were characterized with Fourier transform infrared, H-1 NMR, and Si-29 NMR. The thermal stability of the hybrid polymers was increased with an increasing ratio of POSS moieties as the inorganic part. Because of the steric hindrance caused by the bulkiness of the POSS macromonomer, the number-average molecular weight of the hybrid polymers gradually decreased as the molar percentage of POSS in the feed increased. Their liquid crystallinities were very dependent on the POSS segments of the hybrid polymers behaving as hard, compact components. The hybrid polymer with 90 mol % LC moiety (Cube-LC90) showed liquid crystallinity, larger glass-transition temperatures, and better stability with respect to the LC homopolymer. The results of differential scanning calorimetry and optical polarizing microscopy showed that Cube-LC90 had a smectic-mesophase-like fine-grained texture.