Jianglei Zhang

Jianglei Zhang


Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

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

Representative Publications

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29 October 2020 in Chemical Communications
Verified
Journal Article
Closed access
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WZWeijie Zhang
Weijie Zhang
HWHe Wang
He Wang
FLFeng Li
Feng Li
YCYuncong Chen
Yuncong Chen
RKRyan T. K. Kwok
Ryan T. K. Kwok
Ben Zhong TangBen Zhong Tang
Ben Zhong Tang
A high performance ratiometric fluorescent probe, namely TPE-RNS, has been developed for detecting exogenous and endogenous HClO/ClO− in living cells and discriminating cancer cells from normal cells.

7 June 2021 in Molecular Biotechnology
Verified
Journal Article
Closed access
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JWJin Wang
Jin Wang
XCXiaojuan Chen
Xiaojuan Chen
CXChen Xie
Chen Xie
MSMingbing Sun
Mingbing Sun
CHChenrui Hu
Chenrui Hu
XZXin Zhao
Xin Zhao

1 April 2023 in Experimental and Clinical Transplantation
Verified
Journal Article
Closed access
JLJianhua Long
Jianhua Long
ZFZhimin Feng
Zhimin Feng
HZHuidong Zhou
Huidong Zhou
JLJia Liu
Jia Liu
JZJianglei Zhang
Jianglei Zhang
JOJun Ouyang
Jun Ouyang
Objectives: The incidence of diabetes significantly increases after kidney transplant, and the associated gut microbiota are closely related to diabetes. However, the gut microbiota of recipients with diabetes after kidney transplant remain unexplored. Materials and Methods: Feces samples from recipients with diabetes 3 months after kidney transplant were collected and analyzed using high-throughput 16S rRNA gene sequencing. Results: Our study included 45 transplant recipients: 23 posttransplant diabetes mellitus recipients, 11 recipients without diabetes mellitus, and 11 recipients with preexisting diabetes mellitus. No significant differences in intestinal flora richness and a diversity were observed among the 3 groups. However, principal coordinate analysis based on UniFrac distance revealed significant differences in ss diversity. At the phyla level, the abundance of Proteobacteria in posttransplant diabetes mellitus recipients decreased (P =.028), whereas that of Bactericide (P =.004) increased. At the class level, the abundance of Gammaproteobacteria (P =.037) decreased, whereas that of Bacteroidia (P =.004) increased. At the order level, the abundance of Enterobacteriales (P =.039) decreased, whereas Bacteroidales (P =.004) increased. At the family level, the abundance of Enterobacteriaceae (P =.039) and Peptostreptococcaceae (P =.008) decreased, whereas Bacteroidaceae (P =.010) increased. At the genus level, the abundance of Lachnospiraceae incertae sedis (P =.008) decreased, whereas Bacteroides (P =.010) increased. Furthermore, KEGG analysis identified 33 pathways, among which the biosynthesis of unsaturated fatty acids was closely related to gut microbiota and posttransplant diabetes mellitus. Conclusions: To our knowledge, this is the first comprehensive analysis of the gut microbiota from posttransplant diabetes mellitus recipients. The microbial composition of stool samples of posttransplant diabetes mellitus recipients was significantly different from recipients without diabetes and with preexisting diabetes. The number of bacteria producing short-chain fatty acids decreased, whereas pathogenic bacteria increased.

12 January 2026 in World Journal of Surgical Oncology
Verified
Journal Article
Open access
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HZHuidong Zhou
Huidong Zhou
SPShao Peng
Shao Peng
ZLZhixin Ling
Zhixin Ling
JCJiaodi Cai
Jiaodi Cai
JLJinghong Liu
Jinghong Liu
JZJianglei Zhang
Jianglei Zhang
Bladder cancer (BC) is characterized by a high incidence and frequent recurrence. Despite efforts to improve survival and reduce mortality among BC patient

16 September 2025 in Research Square
Verified
Preprint
Open access
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HZHuidong Zhou
Huidong Zhou
SPShao Peng
Shao Peng
ZLZhixin Ling
Zhixin Ling
JCJiaodi Cai
Jiaodi Cai
JLJinghong Liu
Jinghong Liu
JZJianglei Zhang
Jianglei Zhang
Bladder cancer (BC) is characterized by a high incidence and frequent recurrence. Despite efforts to improve survival and reduce mortality among BC patients, significant progress remains elusive. The role of the cell cycle in BC has been increasingly studied, and our analysis revealed that BC exhibits elevated expression of BUB1 mitotic checkpoint serine/threonine kinase B (BUB1B). However, the role of BUB1B in BC remains not fully understood. A Multi-omics analysis was performed by integrating BUB1B expression with clinical data, and the results indicated that the upregulation of BUB1B was associated with poor prognosis. Moreover, our study demonstrated that BUB1B promotes bladder cancer (BC) cell proliferation, migration, invasion, and tumorigenicity both in vitro and in vivo . Finally, sequencing results revealed that overexpression of BUB1B resulted in the reduction of certain chemokines and was positively correlated with cell cycle-related proteins. These findings provided insights into the potential role of BUB1B as a therapeutic target for BC.