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Shuyang Chen Laboratory

❮Cancer Biology Shuyang Chen Laboratory
  • Shuyang Chen Laboratory
  • Principal Investigator
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Principal Investigator

Shuyang Chen Headshot

Shuyang Chen, PhD

Assistant Staff
Email: [email protected]
Location: Cleveland Clinic Main Campus

Research

The Shuyang Chen lab has primary research interests in the environmental and genetic factors contributing to melanoma development.


Biography

Dr. Shuyang Chen is an Assistant Staff in the Department of Cancer Biology at Cleveland Clinic and an Assistant Professor at Cleveland Clinic Lerner College of Medicine (CCLCM) of Case Western Reserve University (CWRU). 


Education & Professional Highlights

Ph.D. in Biological Science, Drexel University, Philadelphia, PA

B.S. in Biological Science, University of Science and Technology of China, Hefei, China

 

Research

Research

Overview

In the United States, about 1/50 Americans are diagnosed with melanoma, and melanoma incidence increases at an estimated rate of 3% yearly. The Chen lab has primary research interests in the environmental and genetic factors contributing to melanoma development. One of our research is focusing on the reasons redheaded people are more likely to develop melanoma. Melanoma disproportionately affects redheads, as mutations in the melanocortin-1 receptor (MC1R), known to control the melanocyte cells producing pigment, make these redheads unable to tan or have pigmentation to protect their skin. Currently, the lab is using physiologically relevant animal models to study the role of MC1R in melanoma development. Expected outcomes will bring novel insights into the mechanisms of melanoma development and identify novel intervention strategies to combat melanoma.

Our Team

Our Team

Publications

Selected Publications

Selected publications:

1. Sun Y, Li X, Yin C, Zhang J, Liang E, Wu X, Ni Y, Arbesman J, Goding CR, Chen S. AMPK phosphorylates ZDHHC13 to increase MC1R activity and suppress melanomagenesis. Cancer Res. 2023 Jan 26; PubMed PMID: 36701140.

2. Park J, Zhao Y, Zhang F, Zhang S, Kwong AC, Zhang Y, Hoffmann HH, Bushweller L, Wu X, Ashbrook AW, Stefanovic B, Chen S, Branch AD, Mason CE, Jung JU, Rice CM, Wu X. IL-6/STAT3 axis dictates the PNPLA3-mediated susceptibility to non-alcoholic fatty liver disease. J Hepatol. 2023 Jan;78(1):45-56. doi: 10.1016/j.jhep.2022.08.022. PubMed PMID: 36049612; PubMed Central PMCID: PMC9772150.

3. Yin C, Zhu B, Zhang T, Liu T, Chen S, Liu Y, Li X, Miao X, Li S, Mi X, Zhang J, Li L, Wei G, Xu ZX, Gao X, Huang C, Wei Z, Goding CR, Wang P, Deng X, Cui R. Pharmacological Targeting of STK19 Inhibits Oncogenic NRAS-Driven Melanomagenesis. Cell. 2019 Feb 21;176(5):1113-1127.e16. doi: 10.1016/j.cell.2019.01.002. Epub 2019 Jan 31. PubMed PMID: 30712867.

4. Chen S, Han C, Miao X, Li X, Yin C, Zou J, Liu M, Li S, Stawski L, Zhu B, Shi Q, Xu ZX, Li C, Goding CR, Zhou J, Cui R. Targeting MC1R depalmitoylation to prevent melanomagenesis in redheads. Nat Commun. 2019 Feb 20;10(1):877. doi: 10.1038/s41467-019-08691-3. PubMed PMID: 30787281; PubMed Central PMCID: PMC6382811.

5. Zhu B, Tang L, Chen S, Yin C, Peng S, Li X, Liu T, Liu W, Han C, Stawski L, Xu ZX, Zhou G, Chen X, Gao X, Goding CR, Xu N, Cui R, Cao P. Targeting the upstream transcriptional activator of PD-L1 as an alternative strategy in melanoma therapy. Oncogene. 2018 Sep;37(36):4941-4954. doi: 10.1038/s41388-018-0314-0. Epub 2018 May 22. PubMed PMID: 29786078.

6. Zhu B, Chen S, Wang H, Yin C, Han C, Peng C, Liu Z, Wan L, Zhang X, Zhang J, Lian CG, Ma P, Xu ZX, Prince S, Wang T, Gao X, Shi Y, Liu D, Liu M, Wei W, Wei Z, Pan J, Wang Y, Xuan Z, Hess J, Hayward NK, Goding CR, Chen X, Zhou J, Cui R. The protective role of DOT1L in UV-induced melanomagenesis. Nat Commun. 2018 Jan 17;9(1):259. doi: 10.1038/s41467-017-02687-7. PubMed PMID: 29343685; PubMed Central PMCID: PMC5772495.

7. Chen S, Zhu B, Yin C, Liu W, Han C, Chen B, Liu T, Li X, Chen X, Li C, Hu L, Zhou J, Xu ZX, Gao X, Wu X, Goding CR, Cui R. Palmitoylation-dependent activation of MC1R prevents melanomagenesis. Nature. 2017 Sep 21;549(7672):399-403. doi: 10.1038/nature23887. Epub 2017 Sep 6. PubMed PMID: 28869973; PubMed Central PMCID: PMC5902815.

8. Robles-Espinoza CD, Roberts ND, Chen S, Leacy FP, Alexandrov LB, Pornputtapong N, Halaban R, Krauthammer M, Cui R, Timothy Bishop D, Adams DJ. Germline MC1R status influences somatic mutation burden in melanoma. Nat Commun. 2016 Jul 12;7:12064. doi: 10.1038/ncomms12064. PubMed PMID: 27403562; PubMed Central PMCID: PMC4945874.

Careers

Careers

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Our education and training programs offer hands-on experience at one of the nationʼs top hospitals. Travel, publish in high impact journals and collaborate with investigators to solve real-world biomedical research questions.

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