Advanced in vitro cervical tumor model was established by 3D printing to study the epithelial-to-mesenchymal transition (EMT), which is a very important stage of dissemination of carcinoma leading to metastatic tumors. A Hela/hydrogel grid construct composed of gelatin, alginate, matrigel and Hela cells was fabricated by forced extrusion in a layer-by-layer fashion. Hela cells rapidly proliferated, formed spheroids and presented tumorigenic characteristic in the 3D-printed structure. With the supplement of TGF-β, aggregated Hela cells started to disintegrate, and some of them changed into fibroblast-like spindle morphology, which indicate epithelial-to-mesenchymal transition was induced. The down-regulation of epithelial marker E-cadherin, and up-regulation of mesenchymal markers like snail, vimentin and N-cadherin were all observed in 3D-printed model, and performed differently in 3D and 2D models. The TGF-β induced EMT was inhibited by the treatment of disulfiram and EMT pathway inhibitor C19 in a dose dependent manner, showing a great potential in future study of therapeutic program towards cervical tumor metastasis.