Pengfei Jiang

Dr. Pengfei Jiang

Department of Microbiology & Immunology, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou 325035, Zhejiang, P. R. China
orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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Verified
Journal Article
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PJPengfei Jiang
Pengfei Jiang
DZDeli Zhang
Deli Zhang
Maternal embryonic leucine zipper kinase (MELK) functions as a modulator of intracellular signaling and affects various cellular and biological processes, including cell cycle, cell proliferation, apoptosis, spliceosome assembly, gene expression, embryonic development, hematopoiesis, and oncogenesis. In these cellular processes, MELK functions by binding to numerous proteins. In general, the effects of multiple protein interactions with MELK are oncogenic in nature, and the overexpression of MELK in kinds of cancer provides some evidence that it may be involved in tumorigenic process. In this review, our current knowledge of MELK function and recent discoveries in MELK signaling pathway were discussed. The regulation of MELK in cancers and its potential as a therapeutic target were also described.

1 May 2017 in Vaccine
Verified
Journal Article
Closed access
PJPengfei Jiang
Pengfei Jiang
YCYiqi Cai
Yiqi Cai
JCJun Chen
Jun Chen
XYXiaoxian Ye
Xiaoxian Ye
SMShanshan Mao
Shanshan Mao
LZLifang Zhang
Lifang Zhang

1 January 2019 in Emerging Microbes & Infections
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Journal Article
Open access
NCNancy M. Cladel
Nancy M. Cladel
PJPengfei Jiang
Pengfei Jiang
JLJingwei J. Li
Jingwei J. Li
XPXuwen Peng
Xuwen Peng
TCTimothy K. Cooper
Timothy K. Cooper
Jiafen HuJiafen Hu
Jiafen Hu
Human papillomaviruses (HPV) contribute to most cervical cancers and are considered to be sexually transmitted. However, papillomaviruses are often found in cancers of internal organs, including the stomach, raising the question as to how the viruses gain access to these sites. A possible connection between blood transfusion and HPV-associated disease has not received much attention. Here we show, in rabbit and mouse models, that blood infected with papillomavirus yields infections at permissive sites with detectable viral DNA, RNA transcripts, and protein products. The rabbit skin tumours induced via blood infection displayed decreased expression of SLN, TAC1, MYH8, PGAM2, and APOBEC2 and increased expression of SDRC7, KRT16, S100A9, IL36G, and FABP9, as seen in tumours induced by local infections. Furthermore, we demonstrate that blood from infected mice can transmit the infection to uninfected animals. Finally, we demonstrate the presence of papillomavirus infections and virus-induced hyperplasia in the stomach tissues of animals infected via the blood. These results indicate that blood transmission could be another route for papillomavirus infection, implying that the human blood supply, which is not screened for papillomaviruses, could be a potential source of HPV infection as well as subsequent cancers in tissues not normally associated with the viruses.

13 April 2015 in Cellular & Molecular Immunology
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Journal Article
Closed access
XLXiaoyun Lin
Xiaoyun Lin
SCShao Chen
Shao Chen
XXXiangyang Xue
Xiangyang Xue
LLLijun Lu
Lijun Lu
SZShanli Zhu
Shanli Zhu
LZLifang Zhang
Lifang Zhang

21 September 2016 in Oncotarget
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Journal Article
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XXXiangyang Xue
Xiangyang Xue
BWBingbing Wang
Bingbing Wang
WDWangqi Du
Wangqi Du
CZChanqiong Zhang
Chanqiong Zhang
YSYiling Song
Yiling Song
LZLifang Zhang
Lifang Zhang
Generation of affibody molecules specific for HPV16 E7 recognition

1 January 2018 in Theranostics
Verified
Journal Article
Open access
PJPengfei Jiang
Pengfei Jiang
LWLude Wang
Lude Wang
BHBailong Hou
Bailong Hou
JZJinshun Zhu
Jinshun Zhu
MZMeng Zhou
Meng Zhou
LZLifang Zhang
Lifang Zhang
Cervical cancer, the second most common cause of cancer death in women worldwide, is significantly associated with infection of high-risk human papillomaviruses (HPVs), especially the most common genotype, HPV 16. To date, there is no established noninvasive therapy to treat cervical cancer.