Benserazide is a novel inhibitor targeting PKM2 for melanoma treatment
| Autor: | Cong Peng, Yijing He, JiangLing Zhang, Xiang Chen, Shuang Zhao, Jianda Zhou, Juan Su, Youyou Zhou, Huang Zunnan, Guigui Zhang, Jie Li, Juan Tao, Lisha Wu |
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| Rok vydání: | 2019 |
| Předmět: |
Thyroid Hormones
Cancer Research Antineoplastic Agents Cell Growth Processes PKM2 medicine.disease_cause Benserazide Mice 03 medical and health sciences 0302 clinical medicine Cell Movement In vivo Cell Line Tumor medicine Animals Humans Neoplasm Invasiveness Glycolysis Molecular Targeted Therapy RNA Messenger Melanoma Cell growth Chemistry Membrane Proteins medicine.disease Xenograft Model Antitumor Assays Oncology Anaerobic glycolysis Gene Knockdown Techniques 030220 oncology & carcinogenesis Cancer research Carrier Proteins Carcinogenesis Pyruvate kinase |
| Zdroj: | International Journal of Cancer. 147:139-151 |
| ISSN: | 1097-0215 0020-7136 |
| Popis: | The M2 splice isoform of pyruvate kinase (PKM2) is a key enzyme for generating pyruvate and ATP in the glycolytic pathway, whereas the role of PKM2 in tumorigenesis remains a subject of debate. In our study, we found PKM2 is highly expressed in melanoma patients and the malignance is positively correlated with high PKM2 activity and glycolytic capability in melanoma cells. Suppression of PKM2 expression by knocking down markedly attenuated malignant phenotype both in vitro and in vivo, and restoration of PKM2 expression in PKM2 depleted cells could rescue melanoma cells proliferation, invasion and metastasis. With the data indicating PKM2 as a potential therapeutic target, we performed screening for PKM2 inhibitors and identified benserazide (Ben), a drug currently in clinical use. We demonstrated that Ben directly binds to and blocks PKM2 enzyme activity, leading to inhibition of aerobic glycolysis concurrent up-regulation of OXPHOS. Of note, despite PKM2 is very similar to PKM1, Ben does not affect PKM1 enzyme activity. We showed that Ben significantly inhibits cell proliferation, colony formation, invasion and migration in vitro and in vivo. The specificity of Ben was demonstrated by the findings that, suppression of PKM2 expression diminishes the efficacy of Ben in inhibition of melanoma cell growth; ectopic PKM2 expression in normal cells sensitizes cells to Ben treatment. Interestingly, PKM2 activity and aerobic glycolysis are upregulated in BRAFi-resistant melanoma cells. As a result, BRAFi-resistant cells exhibit heightened sensitivity to suppression of PKM2 expression or treatment with Ben both in vitro and in vivo. |
| Databáze: | OpenAIRE |
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