[논문]Bacterial type III effector protein HopQ inhibits melanoma motility through autophagic degradation of vimentin

Park, Seung-Ho; Yoon, Sung-Jin; Choi, Song; Kim, Jun-Seob; Lee, Moo-Seung; Lee, Seon-Jin; Lee, Sang-Hyun; Min, Jeong-Ki; Son, Mi-Young; Ryu, Choong-Min; Yoo, Jiyun; Park, Young-Jun

doi:10.1038/s41419-020-2427-y

[해외논문] Bacterial type III effector protein HopQ inhibits melanoma motility through autophagic degradation of vimentin 원문보기

Cell death & disease, v.11 no.4, 2020년, pp.231 -

Park, Seung-Ho (Environmental Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea) , Yoon, Sung-Jin (Environmental Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea) , Choi, Song (Environmental Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea) , Kim, Jun-Seob (Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea) , Lee, Moo-Seung (Environmental Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea) , Lee, Seon-Jin (Environmental Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea) , Lee, Sang-Hyun (Biotherapeutics Translational Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea) , Min, Jeong-Ki (University of Science and Technology, Daejeon, Republic o) , Son, Mi-Young , Ryu, Choong-Min , Yoo, Jiyun , Park, Young-Jun

Abstract ▼ AI-Helper

Malignant melanoma is a fatal disease that rapidly spreads to the whole body. Treatments have limited efficiency owing to drug resistance and various side effects. Pseudomonas syringae pv. tomato (Pto) is a model bacterial pathogen capable of systemic infection in plants. Pto injects the effector protein HopQ into the plant cytosol via a type III secretion machinery and suppresses the host immunity. Intriguingly, host plant proteins regulated by HopQ are conserved even in humans and conferred in tumor metastasis. Nevertheless, the potential for HopQ to regulate human cancer metastasis was unknown. In this study, we addressed the suitability of HopQ as a possible drug against melanoma metastasis. In melanoma cells, overexpressed HopQ is phosphorylated and bound to 14-3-3 through its N-terminal domain, resulting in stronger interaction between HopQ and vimentin. The binding of HopQ to vimentin allowed for degradation of vimentin via p62-dependent selective autophagy. Attenuation of vimentin expression by HopQ inhibited melanoma motility and in vivo metastasis. These findings demonstrated that HopQ directly degraded vimentin in melanoma cells and could be applied to an inhibitor of melanoma metastasis.

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