LHLanxiang Huang

Lanxiang Huang

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Lanxiang Huang has a total of 7 co-authors. Here are the top co-authors by number of shared publications:

  • Guogui Sun

    Department of Oncology Radiation Physics Technology Section, North China University of Science and Technology Affiliated Hospital, Tangshan, Hebei, 063000, China; Hebei Key Laboratory of Medical-Industrial Integration Precision Medicine, Tangshan, Hebei, 063000, China

    1 shared publication
  • Wei Liu

    School of Clinical Medicine, North China University of Science and Technology, Tangshan 063200, China

    1 shared publication
  • Wenyue Kong

    School of Clinical Medicine, Affiliated Hospital, North China University of Science and Technology, Tangshan, Hebei Province, China

    1 shared publication
  • Xin Su

    School of Clinical Medicine, North China University of Science and Technology, Tangshan 063200, China

    1 shared publication
  • Xuan Zheng

    The Cancer Institute, Tangshan People’s Hospital, Tangshan, China

    1 shared publication
  • Yingze Zhu

    School of Clinical Medicine, Affiliated Hospital, North China University of Science and Technology, Tangshan, Hebei Province, China

    1 shared publication

Latest Publications

  • Open Access

    Development and Validation of the Oxidative Stress Related lncRNAs for Prognosis in Esophageal Squamous Cell Carcinoma

    by Xuan Zheng, Wei Liu, Yingze Zhu, Wenyue Kong, Xin Su, Lanxiang Huang, Yishuang Cui, Guogui Sun

    Esophageal squamous cell cancer (ESCC) is an aggressive disease associated with a poor prognosis. Long non-coding RNAs (lncRNAs) and oxidative stress play crucial roles in tumor progression. We aimed to identify an oxidative stress-related lncRNA signature that could predict the prognosis in ESCC. In the GSE53625 dataset, we identified 332 differentially expressed lncRNAs (DElncRNAs) between ESCC and control samples, out of which 174 were oxidative stress-related DElncRNAs. Subsequently, seven oxidative stress-related DElncRNAs (CCR5AS, LINC01749, PCDH9-AS1, TMEM220-AS1, KCNMA1-AS1, SNHG1, LINC01672) were selected based on univariate and LASSO Cox to build a prognostic risk model, and their expression was detected by RT-qPCR. The model exhibited an excellent ability for the prediction of overall survival (OS) and other clinicopathological traits using Kaplan–Meier (K-M) survival curves, receiver operating characteristic (ROC) curves, and the Wilcoxon test. Additionally, analysis of infiltrated immune cells and immune checkpoints indicated differences in immune status between the two risk groups. Finally, the in vitro experiments showed that PCDH9-AS1 overexpression inhibited proliferation ability and promoted apoptosis and oxidative stress levels in ESCC cells. In conclusion, our study demonstrated that a novel oxidative stress-related DElncRNA prognostic model performed favorably in predicting ESCC patient prognosis and benefits personalized clinical applications.