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Evaluating the Effectiveness of Cancer Drug Sensitization In Vitro and In Vivo
Published on: February 6, 2015
Cisplatin-induced programmed cell death ligand-2 expression is associated with metastasis ability in oral squamous
Shunichi Sudo1,2, Hiroshi Kajiya1,3, Shinji Okano4
1Department of Physiological Science and Molecular Biology, Fukuoka Dental College, Fukuoka, Japan.
Abstract:
Programmed cell death ligands (PD-Ls) are expressed in tumor cells where they bind to programmed cell death-1, an immunocyte co-receptor, resulting in tumor cell evasion from the immune system. Chemotherapeutic drugs have been recently reported to induce the expression of PD-L, such as PD-L1, in some cancer cells. However, little is known regarding PD-L2 expression and its role in oral squamous cell carcinoma (OSCC). In this study, we examined the effect of cisplatin on the expression and regulation of PD-L2 in OSCC cell lines and analyzed malignant behavior in PD-L2-expressing cells using colony, transwell and transformation assays. In addition, we examined PD-L2 expression in the tumor tissues of OSCC patients using cytology and tissue microarray methods. In OSCC cell lines, cisplatin treatment upregulated PD-L2 expression, along with that of the drug efflux transporter ABCG2, via signal transducers and activator of transcription (STAT) 1/3 activation. Moreover, PD-L2-positive or PD-L2-overexpressing cells demonstrated upregulation in both invasion and transformation ability but not in proliferation compared with PD-L2-negative or PD-L2-silencing cells. PD-L2 expression was also observed in OSCC cells of cytology samples and tissue from OSCC patients. The intensity of PD-L2 expression was correlated with more malignant morphological features in the histological appearance and an invasive pattern. Our findings indicate that cisplatin-upregulated PD-L2 expression in OSCC via STAT1/3 activation and the expression of PD-L2 are likely to be associated with malignancy in OSCC. The PD-L2 expression in cisplatin-resistant OSCC cells may be a critical factor in prognosis of advanced OSCC patients.
Insights
Cisplatin increases programmed cell death ligand-2 (PD-L2) in oral cancer cells, enhancing their invasion and transformation. PD-L2 expression in oral squamous cell carcinoma (OSCC) correlates with malignancy and may impact prognosis.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- Programmed cell death ligands (PD-Ls) mediate tumor immune evasion by binding PD-1.
- Chemotherapy can induce PD-L expression, but PD-L2's role in oral squamous cell carcinoma (OSCC) is unclear.
Purpose of the Study:
- To investigate cisplatin's effect on PD-L2 expression and regulation in OSCC.
- To analyze the impact of PD-L2 on OSCC malignant behaviors.
- To assess PD-L2 expression in patient-derived OSCC samples.
Main Methods:
- OSCC cell lines treated with cisplatin.
- Analysis of PD-L2 and ABCG2 expression via STAT1/3 signaling.
- In vitro assays (colony, transwell, transformation) for PD-L2-expressing cells.
- Cytology and tissue microarray analysis of OSCC patient tumors.
Main Results:
- Cisplatin upregulated PD-L2 and ABCG2 in OSCC cells through STAT1/3 activation.
- PD-L2-expressing cells showed increased invasion and transformation, not proliferation.
- PD-L2 expression was detected in patient OSCC samples.
- Higher PD-L2 intensity correlated with malignant morphology and invasive patterns.
Conclusions:
- Cisplatin induces PD-L2 expression in OSCC via STAT1/3, potentially promoting malignancy.
- PD-L2 expression is linked to OSCC's invasive behavior and malignant features.
- PD-L2 in cisplatin-resistant OSCC cells may serve as a prognostic marker for advanced disease.
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