Malignant transformation and progression in cancer is associated with the altered expression of multiple miRNAs, which are considered as post-transcriptional regulators of genes participating in various cellular processes. Although, it has been proposed that miR-23b-3p acts as a tumor suppressor in cervical cancer (CC), not all the pathways through which it alters the cellular processes have been described. The present study examines whether miR-23b-3p directly represses the c-Met expression and that consequently modifies the proliferation, migration and invasion of C33A and CaSki cells. c-Met has five microRNA response elements (MREs) for miR-23b-3p in the 3′-UTR region. The ectopic overexpression of miR-23b-3p significantly reduces c-Met expression in C33A and CaSki cells. The overexpression of miR-23b-3p reduces proliferation, migration and invasion of CaSki cells and the proliferation and invasion in C33A cells. In CaSki cells, the activation of Gab1 and Fak, downstream of c-Met, is reduced in response to the overexpression of miR-23b-3p. Together, the results in the present study indicate that miR-23b-3p is a tumor suppressor that modulates the progression of CC via posttranscriptional regulation of the c-Met oncogene. Cervical cancer (CC) is the fourth most common malignancy in women around the world, with 569,847 newly diagnosed cases and 311,365 deaths registered in 2018 1. The late detection of CC increases the risk of metastasis and death, with a third of CC patients diagnosed in the advanced stages of the disease 2. This has driven the search for progression and prognosis markers which enable the improvement of treatment scheme selection. While persistent high-risk human papillomavirus (HR HPV) infection plays a central role in the genesis of CC 3 , other factors also contribute to the origin and progression of this malignancy. Some mutations, modifications in specific and global DNA methylation, changes to the expression profiles of chromatin-modifying enzymes and the aberrant expression of microRNAs (miRNAs) are events frequently detected in CC 4,5. Regulating gene