Actions of L-thyroxine and Nano-diamino-tetrac (Nanotetrac) on PD-L1 in cancer cells

作者：Lin Hung Yun; Chin Yu Tang; Nana Andre Wendindonde; Shih Ya Jung; Lai Hsuan Yu; Tang Heng Yuan; Leinung Matthew; Mousa Shaker A; Davis Paul J^*

来源：Steroids, 2016, 114: 59-67.

DOI：10.1016/j.steroids.2016.05.006

• Programmed death ligand 1
• L-Thyroxine (T-4)
• Cancer immunotherapy
• Colon carcinoma
• Breast carcinoma

The PD-1 (programmed death-1)/PD-L1 (PD-ligand 1) checkpoint is a critical regulator of activated T cell cancer cell interactions, defending tumor cells against immune destruction. Nano-diamino-tetrac (NDAT; Nanotetrac) is an anticancer/anti-angiogenic agent targeted to the thyroid hormone-tetrac receptor on the extracellular domain of integrin alpha v beta 3. NDAT inhibits the cancer cell PI3-K and MAPK signal transduction pathways that are critical to PD-L1 gene expression. We examined actions in vitro of thyroid hormone (L-thyroxine, T-4) and NDAT on PD-L1 mRNA abundance (qPCR) and PD-L1 protein content in human breast cancer (MDA-MB-231) cells and colon carcinoma (HCT116 and HT-29) cells. In MDA-MB-231 cells, a physiological concentration of T-4 (10(-7) M total; 10(-10) M free hormone) stimulated PD L1 gene expression by 38% and increased PD-L1 protein by 2.7-fold (p < 0.05, all changes). NDAT (10(-7) M) reduced PD-L1 in T-4-exposed cells by 21% (mRNA) and 39% (protein) (p < 0.05, all changes). In HCT116 cells, T-4 enhanced PD-Ll gene expression by 17% and protein content by 24% (p < 0.05). NDAT reduced basal PD-L1 mRNA by 35% and protein by 31% and in T-4-treated cells lowered mRNA by 33% and protein by 66%. In HT-29 cells, T-4 increased PD-Ll mRNA by 62% and protein by 27%. NDAT lowered basal and T-4-stimulated responses in PD-Ll mRNA and protein by 35-40% (p < 0.05). Activation of ERK1/2 was involved in T-4-induced PD-L1 accumulation. We propose that, by a nongenomic mechanism, endogenous T-4 may clinically support activity of the defensive PD-1/13D-L1 checkpoint in tumor cells. NDAT non-immunologically suppresses basal and T-4-induced PD-L1 gene expression and protein accumulation in cancer cells.

• 出版日期2016-10