Juan Chen

Dr. Juan Chen

orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 September 2022 in Cancers
Verified
Journal Article
Open access
PDF file
YCYuxi Cheng
Yuxi Cheng
JCJuan Chen
Juan Chen
YSYuxin Shi
Yuxin Shi
XFXiaodan Fang
Xiaodan Fang
ZTZhan-Gui Tang
Zhan-Gui Tang
Oral squamous cell carcinoma accounts for 95% of human head and neck squamous cell carcinoma cases. It is highly malignant and aggressive, with a poor prognosis and a 5-year survival rate of <50%. In recent years, basic and clinical studies have been performed on the role of the mitogen-activated protein kinase (MAPK) signaling pathway in oral cancer. The MAPK signaling pathway is activated in over 50% of human oral cancer cases. Herein, we review research progress on the MAPK signaling pathway and its potential therapeutic mechanisms and discuss its molecular targeting to explore its potential as a therapeutic strategy for oral squamous cell carcinoma.

26 November 2021 in Cancers
Verified
Journal Article
Open access
PDF file
Jianfei TangJianfei Tang
Jianfei Tang
XFXiaodan Fang
Xiaodan Fang
JCJuan Chen
Juan Chen
HZHaixia Zhang
Haixia Zhang
ZTZhan-Gui Tang
Zhan-Gui Tang
Oral squamous cell carcinoma (OSCC) is a type of malignancy with high mortality, leading to poor prognosis worldwide. However, the molecular mechanisms underlying OSCC carcinogenesis have not been fully understood. Recently, the discovery and characterization of long non-coding RNAs (lncRNAs) have revealed their regulatory importance in OSCC. Abnormal expression of lncRNAs has been broadly implicated in the initiation and progress of tumors. In this review, we summarize the functions and molecular mechanisms regarding these lncRNAs in OSCC. In addition, we highlight the crosstalk between lncRNA and tumor microenvironment (TME), and discuss the potential applications of lncRNAs as diagnostic and prognostic tools and therapeutic targets in OSCC. Notably, we also discuss lncRNA-targeted therapeutic techniques including CRISPR-Cas9 as well as immune checkpoint therapies to target lncRNA and the PD-1/PD-L1 axis. Therefore, this review presents the future perspectives of lncRNAs in OSCC therapy, but more research is needed to allow the applications of these findings to the clinic.

11 January 2017 in BIO Web of Conferences
Verified
Journal Article
Open access
WSWei Shen
Wei Shen
JCJuan Chen
Juan Chen
XLXiurong Li
Xiurong Li
YJYin Jie
Yin Jie