Oral Biomedicine ›› 2022, Vol. 13 ›› Issue (3): 160-164.

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Effects of MT1-MMP interference on the proliferation and invasive ability of oral squamous cell carcinoma

  

  • Received:2022-07-14 Revised:2022-08-16 Online:2022-09-25 Published:2022-09-29

Abstract: Objective: To detect the expression of membrane type 1 matrix metalloproteinase (MT1-MMP) in oral squamous cell carcinoma (OSCC) and its role on the proliferation and invasive ability of OSCC. Methods: RT-PCR was used to detect the expression of MT1-MMP and E-cadherin in OSCC and adjacent tissues; Small interfering RNA (siRNA) was used in targeted interference MT1-MMP gene in HSC3 cells. The experiment was divided into four groups: siControl group, siMT1-MMP group, siControl+transforming growth factor β1 (TGF-β1) group, siMT1-MMP+TGF-β1 group. CCK-8 method was used to detect cell proliferation of HSC3. Transwell assay was used to detect the invasive ability of cells. The expression of MT1-MMP, E-cadherin, TGF-β signaling pathway related proteins (CUTL1 and Wnt5a) was detected by Western blot. Results: Compared with the adjacent tissues, higher expression of MT1-MMP and lower expression of E-cadherin was exhibited in OSCC(P<0.05); the cell proliferation of HSC3 cells did not change significantly after MT1-MMP interference(P>0.05); compared with siControl group and siMT1-MMP group, the HSC3 cell invasion number in siControl+TGF-β1 group and siMT1-MMP+TGF-β1 group was increased significantly; compared with siControl+TGF-β1 group, the HSC3 cell invasion number in siMT1-MMP+TGF-β1 group was decreased significantly(P<0.01); compared with siControl group, protein expression of MT1-MMP, CUTL1 and Wnt5a increased significantly in siControl+TGF-β1 group, while the expression of E-cadherin decreased(P<0.01); compared with siControl+TGF-β1 group, protein expression of MT1-MMP, CUTL1 and Wnt5a decreased partially in siMT1-MMP+TGF-β1 group, while the expression of E-cadherin increased significantly(P<0.05). Conclusions: MT1-MMP interference may inhibit the invasion of OSCC through regulating the EMT process induced by TGF-β1.

Key words: oral squamous cell carcinoma, membrane type 1 matrix metalloproteinase, E-cadherin, epithelial-mesenchymal transition