Xiaozhong Cheng

Prof. Dr. Xiaozhong Cheng

orcid

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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8 February 2023 in Bioorganic & Medicinal Chemistry Letters
Verified
Journal Article
Closed access
YWYiming Wang
Yiming Wang
GZGuilan Zhu
Guilan Zhu
WWWei Wang
Wei Wang
YZYan Zhang
Yan Zhang
YZYong Zhu
Yong Zhu
XCXiaozhong Cheng
Xiaozhong Cheng

15 July 2022 in Bioorganic & Medicinal Chemistry Letters
Verified
Journal Article
Closed access
YCYajun Chen
Yajun Chen
LJLixuan Jia
Lixuan Jia
GZGuilan Zhu
Guilan Zhu
WWWei Wang
Wei Wang
MGMing Geng
Ming Geng
XCXiaozhong Cheng
Xiaozhong Cheng

26 November 2024 in Amino Acids
Verified
Journal Article
Open access
PDF file
XCXiaozhong Cheng
Xiaozhong Cheng
YZYonghuang Zhang
Yonghuang Zhang
YZYan Zhang
Yan Zhang
YCYajun Chen
Yajun Chen
JCJianli Chen
Jianli Chen
GZGuilan Zhu
Guilan Zhu
Antimicrobial peptides (AMPs) have caught the attention of researchers over the last couple of years due to their unique membrane lytic mechanism for combating antibiotic resistance, which differs from the molecular targets of traditional antibiotics. Although natural AMPs exhibit potential antimicrobial activity against a wide range of microorganisms, some drawbacks, such as toxicity, low antibacterial activity, and high production costs limit their clinical application. To enhance the antimicrobial activity of a series of HSP peptides derived from the natural peptide HSP-1, this study optimized them using a variety of strategies, including net charge, hydrophobic moment, hydrophobicity, and helicity. Optimizing the antimicrobial action of HSP peptides depended mostly on net charge, hydrophobic moment, and hydrophobicity rather than helicity. HSP-M4 may be designed to combat microbial infections because the antimicrobial activity and cytotoxicity assays showed that they exhibited low cytotoxicity and prominent antimicrobial activity, respectively.

2 November 2025 in Biomolecules
Verified
Journal Article
Open access
PDF file
XWXiming Wu
Ximing Wu
MYMingchuan Yang
Mingchuan Yang
HZHailing Zhang
Hailing Zhang
LYLumin Yang
Lumin Yang
YHYufeng He
Yufeng He
GZGuilan Zhu
Guilan Zhu
The imbalance of the renin–angiotensin system (RAS), characterized by the overactivation of the pro-tumor ACE/AngII/AT1R axis, is closely linked to tumor growth, angiogenesis, metastasis, and poor prognosis. Natural polyphenols, such as EGCG and resveratrol, exert anti-cancer effects by dual-regulating RAS: they inhibit the pro-tumor axis by blocking renin, ACE activity, and AT1R expression, while simultaneously activating the protective ACE2/Ang(1-7)/MasR axis. Furthermore, polyphenols and their autoxidation products (e.g., EAOP) modify thiol-containing transmembrane proteins (such as ADAM17 and integrins) and interact with RAS components, further disrupting oncogenic pathways (including MAPK and PI3K/Akt/mTOR) to induce apoptosis, suppress invasion, and reduce oxidative stress. Notably, EAOP exhibits stronger RAS-modulating efficacy than its parent polyphenols. However, challenges such as low bioavailability, insufficient targeting, and limited clinical evidence impede their application. This review provides a comprehensive overview of the anti-cancer mechanisms of polyphenols through RAS regulation, discusses the associated challenges, and proposes potential solutions (including nanodelivery and structural modification) and strategies to advance natural product-based adjuvant treatments.