Shuwei Li
Nanjing Medical University
31 Papers
11 Citations
Shuwei Li is an academic researcher from Nanjing Medical University. The author has contributed to research in topics: Colorectal cancer & Single-nucleotide polymorphism. The author has an hindex of 9, co-authored 31 publications.
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Papers
LncRNA MT1JP functions as a ceRNA in regulating FBXW7 through competitively binding to miR-92a-3p in gastric cancer
Gang Zhang,Shuwei Li,Jiafei Lu,Yuqiu Ge,Qiaoyan Wang,Gaoxiang Ma,Qinghong Zhao,Dongdong Wu,Weida Gong,Mulong Du,Haiyan Chu,Meilin Wang,Aihua Zhang,Zhengdong Zhang +13 more
TL;DR: MT1JP, a down-regulated lncRNA in GC, was associated with malignant tumor phenotypes and survival of GC, and it is suggested that MT1JP may act as a potential therapeutic target and prognosis biomarker for GC.
Association of genetic variants in lncRNA H19 with risk of colorectal cancer in a Chinese population.
Shuwei Li,Yibing Hua,Jing Jin,Haixiao Wang,Mulong Du,Lingjun Zhu,Haiyan Chu,Zhengdong Zhang,Meilin Wang +8 more
TL;DR: The results provided the evidence that rs2839698 in H19 was associated with elevated risk of colorectal cancer, which may be a potential biomarker for predicting coloreCTal cancer susceptibility.
The biogenesis and biological function of PIWI-interacting RNA in cancer.
Silu Chen,Shuai Ben,Junyi Xin,Shuwei Li,Rui Zheng,Hao Wang,Lulu Fan,Mulong Du,Zhengdong Zhang,Meilin Wang +9 more
TL;DR: In this paper, the authors systematically reviewed recent advances in the biogenesis and biological functions of piRNAs and relevant bioinformatics databases with the aim of providing insights into cancer diagnosis and clinical applications.
Genetic variants in m6A modification genes are associated with colorectal cancer risk
Yixuan Meng,Shuwei Li,Dongying Gu,Kaili Xu,Mulong Du,Lingjun Zhu,Haiyan Chu,Zhengdong Zhang,Yuan Wu,Zan Fu,Meilin Wang +10 more
TL;DR: The findings indicated that genetic variants in m6A modification genes might be promising predictors of colorectal cancer risk.
Remote modulation of lncRNA GCLET by risk variant at 16p13 underlying genetic susceptibility to gastric cancer
Mulong Du,Rui Zheng,Gaoxiang Ma,Haiyan Chu,Jiafei Lu,Shuwei Li,Junyi Xin,Na Tong,Gang Zhang,Weizhi Wang,Fulin Qiang,Weida Gong,Qinghong Zhao,Guoquan Tao,Jinfei Chen,Zhifang Jia,Jing Jiang,Guangfu Jin,Zhibin Hu,Hongbing Shen,Meilin Wang,Zhengdong Zhang +21 more
TL;DR: A large-scale cross-ancestry genetic study in 18,852 individuals identified the potential causal variant rs3850997 T>G at 16p13 significantly associated with a decreased risk of gastric cancer and highlighted the genetic functions and implications for the etiology and pathology of cancers.
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