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pmid:33614284

Abnormal expression of HOXD11 promotes the malignant behavior of glioma cells and leads to poor prognosis of glioma patients.

Jialin Wang · Zhendong Liu · Cheng Zhang · Hongbo Wang · Ang Li · Binfeng Liu · Xiaoyu Lian · Zhishuai Ren · Wang Zhang · Yanbiao Wang · Bo Zhang · Bo Pang · Yanzheng Gao

PeerJ · 2021 doi:10.7717/peerj.10820

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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pmid:33614284
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title
Abnormal expression of HOXD11 promotes the malignant behavior of glioma cells and leads to poor prognosis of glioma patients.
doi
10.7717/peerj.10820
pmid
33614284
authors array · 13 items
[0]
Jialin Wang
[1]
Zhendong Liu
[2]
Cheng Zhang
[3]
Hongbo Wang
[4]
Ang Li
[5]
Binfeng Liu
[6]
Xiaoyu Lian
[7]
Zhishuai Ren
[8]
Wang Zhang
[9]
Yanbiao Wang
[10]
Bo Zhang
[11]
Bo Pang
[12]
Yanzheng Gao
journal
PeerJ
year
2021
abstract
BACKGROUND: Homeobox D11 (HOXD11) plays an important role in a variety of cancers, but its precise role in gliomas remains unclear. This study aimed to explore the relationship between HOXD11 and gliomas by combining bioinformatics methods with basic experimental validation. MATERIALS AND METHODS: Obtain gene expression information and clinical information of glioma and non-tumor brain tissue samples from multiple public databases such as TCGA (666 glioma samples), CGGA (749 glioma samples), GEPIA(163 glioblastoma samples and 207 normal control samples), GEO (GSE4290 and GSE15824). Nine cases of glioma tissue and five cases of normal control brain tissue were collected from the clinical department of Henan Provincial People's Hospital for further verification. A series of bioinformatic analysis methods were used to confirm the relationship between HOXD11 expression and overall survival and clinical molecular characteristics of patients with glioma. RT-qPCR was used to verify the change of expression level of HOXD11 in glioma cells and tissues. MTT assay, colony formation assay, wound-healing assay, immunofluorescence staining, flow cytometry and western blotting were used to detect the effect of HOXD11 on the biological behavior of glioma cell line U251. RESULTS: The high expression of HOXD11 was significantly related to age, World Health Organization (WHO) grade, chemotherapy status, histological type, and even 1p19q codeletion data and isocitrate dehydrogenase (IDH) mutation. HOXD11, as an independent risk factor, reduces the overall survival of glioma patients and has diagnostic value for the prognosis of glioma. Gene Set Enrichment Analysis (GSEA) showed that HOXD11 was significantly enriched in cell signaling pathway such as cell cycle, DNA replication and so on. Finally, we confirmed that the knockout of HOXD11 can inhibit the proliferation and invasion of U251 glioma cells, and change the biological behavior of tumor cells by preventing the progression of cell cycle. CONCLUSIONS: HOXD11 may be used as a candidate biomarker for the clinical application of targeted drug and prognostic assessment treatment of glioma. In addition, This study will help to explore the pathological mechanism of glioma.
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The relationship between the Overall Survival rate of patients and the expression level of HOXD11 was analyzed by the Kaplan–Meier method and Cox regression analysis, and the survival curve was drawn accordingly.
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The relationship between the Overall Survival rate of patients and the expression level of HOXD11 was analyzed by the Kaplan–Meier method and Cox regression analysis, and the survival curve was drawn accordingly.
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Determination of HOXD11-related cellular signaling pathway by GSEA
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33614284", "kind": "science-record", "revision": 7, "content_hash": "sha256:ecadeddaa65db81be9b3592700f4f722b4b9f4a645ecf0e8fbfea6d6614c688c", "created_at": "2026-11-01T15:41:26Z", "updated_at": "2026-11-01T22:03:09Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Abnormal expression of HOXD11 promotes the malignant behavior of glioma cells and leads to poor prognosis of glioma patients.", "doi": "10.7717/peerj.10820", "pmid": "33614284", "authors": ["Jialin Wang", "Zhendong Liu", "Cheng Zhang", "Hongbo Wang", "Ang Li", "Binfeng Liu", "Xiaoyu Lian", "Zhishuai Ren", "Wang Zhang", "Yanbiao Wang", "Bo Zhang", "Bo Pang", "Yanzheng Gao"], "journal": "PeerJ", "year": 2021, "abstract": "BACKGROUND: Homeobox D11 (HOXD11) plays an important role in a variety of cancers, but its precise role in gliomas remains unclear. This study aimed to explore the relationship between HOXD11 and gliomas by combining bioinformatics methods with basic experimental validation.\nMATERIALS AND METHODS: Obtain gene expression information and clinical information of glioma and non-tumor brain tissue samples from multiple public databases such as TCGA (666 glioma samples), CGGA (749 glioma samples), GEPIA(163 glioblastoma samples and 207 normal control samples), GEO (GSE4290 and GSE15824). Nine cases of glioma tissue and five cases of normal control brain tissue were collected from the clinical department of Henan Provincial People's Hospital for further verification. A series of bioinformatic analysis methods were used to confirm the relationship between HOXD11 expression and overall survival and clinical molecular characteristics of patients with glioma. RT-qPCR was used to verify the change of expression level of HOXD11 in glioma cells and tissues. MTT assay, colony formation assay, wound-healing assay, immunofluorescence staining, flow cytometry and western blotting were used to detect the effect of HOXD11 on the biological behavior of glioma cell line U251.\nRESULTS: The high expression of HOXD11 was significantly related to age, World Health Organization (WHO) grade, chemotherapy status, histological type, and even 1p19q codeletion data and isocitrate dehydrogenase (IDH) mutation. HOXD11, as an independent risk factor, reduces the overall survival of glioma patients and has diagnostic value for the prognosis of glioma. Gene Set Enrichment Analysis (GSEA) showed that HOXD11 was significantly enriched in cell signaling pathway such as cell cycle, DNA replication and so on. Finally, we confirmed that the knockout of HOXD11 can inhibit the proliferation and invasion of U251 glioma cells, and change the biological behavior of tumor cells by preventing the progression of cell cycle.\nCONCLUSIONS: HOXD11 may be used as a candidate biomarker for the clinical application of targeted drug and prognostic assessment treatment of glioma. 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