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Updated: May 26, 2026

Genome-Wide CRISPR Screen for Unveiling Radiosensitive and Radioresistant Genes
Published on: May 23, 2025
RNAi-mediated ERBB2 gene knockdown sensitizes human colorectal cancer cells to radiation
Dong-Li Zhao1, Cheng-Xue Dang, Yan-Xia Sui
1Department of Oncology, First Affiliated Hospital, Medical College of Xi'an Jiaotong University, Xi'an 710061, PR China.
Abstract:
This study aimed to investigate the involvement of c-erbB-2, encoded by the receptor tyrosine kinase ERBB2 gene, in the pathogenesis of colorectal cancer and to validate its potential as an anticancer target. Immunohistochemical and histopathological analyses were applied in tissue samples derived from 80 colorectal cancer patients. ERBB2 stable small hairpin RNA (shRNA) knockdown in HT29 human colorectal cancer cells was confirmed by RT-PCR and western blotting. Cell cycle profile and apoptosis were measured using PI or Annexin V-PI dual staining. A significant correlation between ERBB2 levels and Dukes' stage of colorectal cancer, in both the primary malignancy and lymph node metastatic tissues, was observed. ERBB2-depleted HT-29 cells exhibited increased sensitivity to radiation compared to control cells, likely due to enhanced G0/G1 phase cell cycle arrest and apoptosis. ERBB2 may be involved in the malignancy and metastasis of colorectal cancer. Overexpressed ERBB2 may constitute a potential target for colorectal cancer therapy.
Insights
The receptor tyrosine kinase ERBB2 (also known as c-erbB-2) is implicated in colorectal cancer progression and metastasis. Targeting ERBB2 may offer a new therapeutic strategy for colorectal cancer patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The receptor tyrosine kinase ERBB2 (c-erbB-2) gene plays a role in various cancers.
- Its specific involvement in colorectal cancer pathogenesis and metastatic potential requires further investigation.
Purpose of the Study:
- To investigate the role of ERBB2 in colorectal cancer development and metastasis.
- To evaluate ERBB2 as a potential therapeutic target for colorectal cancer.
Main Methods:
- Immunohistochemical and histopathological analyses of 80 colorectal cancer patient samples.
- ERBB2 knockdown in HT29 cells using small hairpin RNA (shRNA).
- Validation of knockdown via RT-PCR and western blotting; cell cycle and apoptosis assays.
Main Results:
- A significant correlation was found between ERBB2 levels and Dukes' stage in primary and metastatic colorectal cancer tissues.
- ERBB2-depleted cells showed increased sensitivity to radiation, linked to G0/G1 cell cycle arrest and apoptosis.
- ERBB2 overexpression is associated with colorectal cancer malignancy and metastasis.
Conclusions:
- ERBB2 is implicated in the progression and metastasis of colorectal cancer.
- Overexpressed ERBB2 represents a potential therapeutic target for colorectal cancer treatment.
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