PD-L1 Promotes Self-Renewal and Tumorigenicity of Malignant Melanoma Initiating Cells

Abstract EN

Recent studies have indicated that therapeutic antibodies targeting PD-L1 show remarkable efficacy in clinical trials in multiple tumors and that a melanoma cell-intrinsic PD-1: PD-L1 axis promotes tumor growth.

However, few studies have shown tumor-intrinsic PD-L1 effects in malignant melanoma initiating cells (MMICs).

Here, we aim to determine the possible regulatory effects of PD-L1 on MMICs.

The ALDEFLUOR kit was used to identify ALDH+ MMICs.

Flow cytometry was used to examine the expression of PD-L1 on ALDH+ MMICs.

To determine the role of PD-L1 in MMICs self-renewal, we cultured melanoma cells with anti-PD-L1 and measured tumorsphere formation and apoptosis.

In addition, the effects of anti-PD-L1 on tumorigenicity and residual ALDH+ MMICs in tumors were evaluated in vivo.

We demonstrated that melanoma cell-intrinsic PD-L1 was expressed in ALDH+ MMICs.

Blocking PD-L1 in melanoma cell lines impaired tumorsphere formation and induced the apoptosis of sphere cells.

In addition, blocking PD-L1 inhibited tumor growth in vivo.

We observed residual ALDH+ MMICs within the tumor.

The results showed that blocking PD-L1 also significantly decreased the residual ALDH+ MMICs in the tumors.

In conclusion, these results suggest a new mechanism underlying melanoma progression and PD-L1-targeted therapy, which is distinct from the immunomodulatory actions of PD-L1.