Qing Yang

Dr. Qing Yang

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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25 October 2013 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
SYShuangshuang Yang
Shuangshuang Yang
XLXishuai Li
Xishuai Li
FHFangfang Hu
Fangfang Hu
YLYinlong Li
Yinlong Li
YYYunyun Yang
Yunyun Yang
QYQing Yang
Qing Yang

21 February 2020 in Signal Transduction and Targeted Therapy
Verified
Journal Article
Open access
PDF file
LDLisha Du
Lisha Du
ZXZikang Xing
Zikang Xing
BTBangbao Tao
Bangbao Tao
TLTianqi Li
Tianqi Li
DYDan Yang
Dan Yang
QYQing Yang
Qing Yang
Indoleamine 2,3-dioxygenase 1 (IDO1), indoleamine 2,3-dioxygenase 2 (IDO2), and tryptophan 2,3-dioxygenase (TDO) initiate the first step of the kynurenine pathway (KP), leading to the transformation of l-tryptophan (Trp) into l-kynurenine (Kyn) and other downstream metabolites. Kyn is known as an endogenous ligand of the aryl hydrocarbon receptor (AhR). Activation of AhR through TDO-derived Kyn is a novel mechanism to support tumor growth in gliomas. However, the role of IDO1 and IDO2 in this mechanism is still unknown. Herein, by using clinical samples, we found that the expression and activity of IDO1 and/or TDO (IDO1/TDO) rather than IDO2 were positively correlated with the pathologic grades of gliomas. The expression of IDO1/TDO rather than IDO2 was positively correlated with the Ki67 index and overall survival. The expression of IDO1/TDO was positively correlated with the expression of aquaporin 4 (AQP4), implying the potential involvement of IDO1/TDO in glioma cell motility. Mechanistically, we found that IDO1/TDO accounted for the release of Kyn, which activated AhR to promote cell motility via the Kyn–AhR–AQP4 signaling pathway in U87MG glioma cells. RY103, an IDO1/TDO dual inhibitor, could block the IDO1/TDO–Kyn–AhR–AQP4 signaling pathway and exert anti-glioma effects in GL261 orthotopic glioma mice. Together, our results showed that the IDO1/TDO–Kyn–AhR–AQP4 signaling pathway is a new mechanism underlying the malignancy of gliomas, and suggest that both IDO1 and TDO might be valuable therapeutic targets for gliomas.

20 February 2017 in The FEBS Journal
Verified
Journal Article
Closed access
PDF file
YLYang Li
Yang Li
NHNan Hu
Nan Hu
DYDan Yang
Dan Yang
GOGregory Oxenkrug
Gregory Oxenkrug
QYQing Yang
Qing Yang

30 October 2014 in Journal of Alzheimer’s Disease
Verified
Journal Article
Closed access
PDF file
DYDan Yu
Dan Yu
BTBang-Bao Tao
Bang-Bao Tao
YYYun-Yun Yang
Yun-Yun Yang
LDLi-Sha Du
Li-Sha Du
SYShuang-Shuang Yang
Shuang-Shuang Yang
QYQing Yang
Qing Yang
Indoleamine 2,3-dioxygenase (IDO), the first and rate-limiting enzyme in the kynurenine pathway (KP) of tryptophan catabolism, was recently established as one of the potential players involved in the pathogenesis of Alzheimer's disease (AD). Coptisin

28 September 2010 in Journal of Alzheimer’s Disease
Verified
Journal Article
Closed access
PDF file
CYCun-Jing Yu
Cun-Jing Yu
MZMao-Fa Zheng
Mao-Fa Zheng
CKChun-Xiang Kuang
Chun-Xiang Kuang
WHWei-Da Huang
Wei-Da Huang
QYQing Yang
Qing Yang
A well-known traditional Chinese medicinal prescription, Oren-gedoku-to (OGT), has been used in clinical therapies for many types of dementia in China and Japan. Additionally, it ameliorates the age-related deterioration of learning and memory in an

3 October 2019 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
DYDan Yang
Dan Yang
SZShengnan Zhang
Shengnan Zhang
XFXin Fang
Xin Fang
LGLeilei Guo
Leilei Guo
NHNan Hu
Nan Hu
QYQing Yang
Qing Yang