Oral squamous cell carcinoma (
OSCC
) is one of the most common head and neck malignancies. Advanced stages of the disease are associated with poor survival, highlighting a need for new treatment modalities. We previously showed that the proinflammatory cytokine interleukin‐18 (
IL
‐18) has a tumor suppressive role in
OSCC
. Here, we investigated the effects of
IL
‐18 on proliferation, migration, and invasion of
OSCC
cells
ex vivo
and
in vitro
, and in nude mouse xenografts. We report that expression of tankyrase 2 (
TNKS
2), β‐catenin, and N‐cadherin was higher in tumor cells than in normal mucosae, whereas the expression of
IL
‐18 and E‐cadherin was higher in normal than in tumor tissues. Elevated expression of
IL
‐18 (
P
<
0.01) and E‐cadherin (
P
=
0.034) was associated with tumor differentiation, whereas expression of
TNKS
2 (
P
<
0.01), β‐catenin (
P
= 0.012), and N‐cadherin (
P
< 0.01) was associated with tumor de‐differentiation. Furthermore, compared with the vector control,
IL
‐18 overexpression promoted tumor cell migration and invasion (
P
<
0.01), but inhibited growth of tumor cell xenografts (
P
<
0.05). At the protein level, expression levels of
IL
‐18 (
P
<
0.01),
TNKS
2 (
P
= 0.045), β‐catenin (
P
= 0.028), and N‐cadherin (
P
= 0.068) were upregulated in tumor cells after
IL
‐18 overexpression compared with those of the vector control mice, whereas expression levels of E‐cadherin (
P
= 0.045) were decreased. In conclusion, our data suggest that
IL
‐18 overexpression induces oral
SCC
cell invasion and metastasis by promoting the tumor cell epithelial–mesenchymal transition via the Wnt/β‐catenin signaling pathway.