Potential therapeutic targets of the nuclear division cycle 80 (NDC80) complexes genes in lung adenocarcinoma
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Updated: Dec 25, 2025

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
Published on: September 20, 2016
Zhong-Yi Sun1, Wei Wang1, Han Gao2
1Department of Emergency, the First Affiliated Hospital, Guangxi Medical University, Nanning, Guangxi, People's Republic of China.
Abstract:
Background: Lung cancer is the most common cancer worldwide, both in terms of the incidence and mortality. NDC80 complex comprising of NDC80, NUF2, SPC24, and SPC25 is a heterotetrameric protein complex located in the outer layer of the kinetochore and plays a critical role in mitosis. This study focuses on the effects of NDC80 complex genes on clinical features and prognosis in lung adenocarcinoma (LUAD). Materials and methods: Expression of NDC80 complex in LUAD and related clinical information was extracted from the TCGA website. NDC80 complex gene functional analysis and correlation analysis was conducted by using DAVID, BiNGO, Gene MANIA, STRING and GSEA. Survival probability was predicted by nomogram. Statistical analysis was used to predict NDC80 complex gene expression on clinical features and prognosis in patients with LUAD. Results: Expression of NDC80, NUF2, SPC24 and SPC25 was significantly elevated in LUAD tumors compared with normal tissues (P < 0.05). These genes showed diagnostic values for LUAD (P < 0.001 for each; area under the curve (AUC), 0.958, 0.968, 0.951, and 0.932 respectively); combinatorial analysis of these genes was more advantageous than single analysis alone (P < 0.001; AUC > 0.900 for each). Expression of both NDC80 and SPC25 correlated with the prognosis of LUAD (P < 0.001; AUC > 0.600 for each). Higher expression of NDC80, NUF2, SPC24 and SPC25 was associated with low overall survival (OS) in univariate analysis. Higher expression of NDC80 and SPC25 was associated with low OS in multivariate analysis. High expression of NDC80 combined with high expression of SPC25 was predictive of poor OS in LUAD in joint analysis. Conclusion: NDC80 complex gene might be an early indicator of diagnosis and prognosis of LUAD. The combined detection of NDC80, NUF2, SPC24 and SPC25 may become a new research direction in LUAD diagnosis and a new target for tumor targeted gene therapy.
Insights
The NDC80 complex genes (NDC80, NUF2, SPC24, SPC25) are elevated in lung adenocarcinoma (LUAD), showing diagnostic value. Higher expression of NDC80 and SPC25 indicates poor prognosis, suggesting their potential as diagnostic and therapeutic targets for LUAD.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Lung adenocarcinoma (LUAD) is a leading cause of cancer-related death globally.
- The NDC80 complex, crucial for mitosis, comprises NDC80, NUF2, SPC24, and SPC25.
- Dysregulation of the NDC80 complex may contribute to LUAD development and progression.
Purpose of the Study:
- To investigate the role of NDC80 complex genes in LUAD.
- To evaluate the diagnostic and prognostic significance of NDC80 complex gene expression in LUAD patients.
Main Methods:
- Gene expression data and clinical information for LUAD were obtained from The Cancer Genome Atlas (TCGA).
- Functional and correlation analyses were performed using DAVID, BiNGO, Gene MANIA, STRING, and Gene Set Enrichment Analysis (GSEA).
- Prognostic prediction was conducted using nomograms and statistical analyses, including univariate and multivariate approaches.
Main Results:
- NDC80, NUF2, SPC24, and SPC25 genes were significantly overexpressed in LUAD tissues compared to normal tissues.
- These genes demonstrated high diagnostic accuracy for LUAD, with combined analysis outperforming single-gene analysis.
- Elevated expression of NDC80 and SPC25 correlated with poor overall survival (OS) in LUAD patients.
Conclusions:
- NDC80 complex genes may serve as early diagnostic biomarkers for LUAD.
- Combined detection of NDC80, NUF2, SPC24, and SPC25 holds promise for LUAD diagnosis.
- The NDC80 complex represents a potential therapeutic target for LUAD gene therapy.
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