Chengzhou Zhao

Chengzhou Zhao


Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

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

Representative Publications

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1 January 2022 in Journal of Plant Physiology
Verified
Journal Article
Closed access
JQJuan Qin
Juan Qin
CZChengzhou Zhao
Chengzhou Zhao
SWShengwang Wang
Shengwang Wang
NGNa Gao
Na Gao
XWXiangxiang Wang
Xiangxiang Wang
YBYurong Bi
Yurong Bi

19 August 2022 in Molecules
Verified
Journal Article
Open access
PDF file
GDGuozhen Duan
Guozhen Duan
GDGuozhen Duan
Guozhen Duan
DWDengbang Wei
Dengbang Wei
CZChengzhou Zhao
Chengzhou Zhao
YMYonggui Ma
Yonggui Ma
The G-protein-coupled bile acid receptor, Gpbar1 or TGR5, is characterized as a membrane receptor specifically activated by bile acids. A series of evidence shows that TGR5 induces protein kinase B (AKT), nuclear factor kappa-B (NF-κB), extracellular regulated protein kinases (ERK1/2), signal transducer and activator of transcription 3 (STAT3), cyclic adenosine monophosphate (cAMP), Ras homolog family member A (RhoA), exchange protein activated by cAMP (Epac), and transient receptor potential ankyrin subtype 1 protein (TRPA1) signaling pathways, thereby regulating proliferation, inflammation, adhesion, migration, insulin release, muscle relaxation, and cancer development. TGR5 is widely distributed in the brain, lung, heart, liver, spleen, pancreas, kidney, stomach, jejunum, ileum, colon, brown adipose tissue (BAT), white adipose tissue (WAT), and skeletal muscle. Several recent studies have demonstrated that TGR5 exerts inconsistent effects in different cancer cells upon activating via TGR5 agonists, such as INT-777, ursodeoxycholic acid (UDCA), and taurolithocholic acid (TLCA). In this review, we discuss both the ‘friend’ and ‘foe’ features of TGR5 by summarizing its tumor-suppressing and oncogenic functions and mechanisms.

4 March 2022 in Mitochondrial DNA Part B
Verified
Journal Article
Open access
XWXiaoyu Wang
Xiaoyu Wang
JHJing He
Jing He
XSXueping Su
Xueping Su
BXBixiang Xu
Bixiang Xu
YLYan Liu
Yan Liu
CZChengzhou Zhao
Chengzhou Zhao
In the present study, the complete chloroplast genome of Lonicera tangutica is presented and characterized for the first time. The complete chloroplast genome was 156,121 bp in length, including 23,899 bp inverted repeat (IR) regions, an 89,466 bp large single-copy (LSC) region, and an 18,851 bp small single-copy (SSC) region. A total of 129 genes, including 37 tRNA genes, eight rRNA genes, and 84 protein-coding genes, were annotated, and the overall GC content of the chloroplast genome was 38.35%. Two introns in the ycf3 gene and a single intron in another gene were detected. Maximum-likelihood phylogenetic analysis indicated that L. tangutica has a very close evolutionary relationship with Lonicera praeflorens, Lonicera hispida, Lonicera fragrantissima, and Lonicera stephanocarpa. These results are valuable for studying the evolution and genetic diversity of L. tangutica.