A phase 0 trial of riluzole in patients with resectable stage III and IV melanoma

利鲁唑对可切除 III 期和 IV 期黑色素瘤患者的 0 期试验

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作者:Dana Yip, Maithao N Le, Joseph L-K Chan, Jonathan H Lee, Janice A Mehnert, Anthony Yudd, Jeffery Kempf, Weichung J Shih, Suzie Chen, James S Goydos

Conclusions

Our data show that glutamate blockade with riluzole can inhibit signaling through the mitogen-activated protein kinase and phosphatidylinositol 3-kinase/AKT pathways and suppress the metabolic activity of melanoma. The ectopic expression of metabotropic glutamate receptors may be important in the pathogenesis of human melanoma, and targeting this pathway may be an effective therapy.

Purpose

Ectopic expression of GRM1 in murine melanocytes

Results

We accrued 12 patients and all expressed GRM1. We found a significant decrease in pAKT and/or pERK in post-treatment tumor samples as compared with pretreatment samples in 4 (34%) patients. These four patients had a significant decrease in FDG-PET intensity post-treatment as well. Two other patients had a clinical response with no corresponding metabolic response; five patients had similar pretreatment and post-treatment FDG-PET scan findings; and one patient had progressive disease. Conclusions: Our data show that glutamate blockade with riluzole can inhibit signaling through the mitogen-activated protein kinase and phosphatidylinositol 3-kinase/AKT pathways and suppress the metabolic activity of melanoma. The ectopic expression of metabotropic glutamate receptors may be important in the pathogenesis of human melanoma, and targeting this pathway may be an effective therapy.

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