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Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer
Published on: March 14, 2019
EGFR, HER2 and HER3 expression in primary colorectal carcinomas and corresponding metastases: Implications for
1Department of Radiation Oncology, the Second Affiliated Hospital, Hangzhou, P.R. China.
Abstract:
Members of the epidermal growth factor receptor, EGFR, family are interesting as targets for radionuclide therapy using targeting agents labeled with α- or β-emitting radionuclides, especially when EGFR-positive colorectal carcinomas, CRC, are resistant to EGFR inhibiting agents like cetuximab and various tyrosine kinase inhibitors. The expression of EGFR, HER2 and HER3 was therefore analyzed in CRC samples from primary tumors, corresponding lymph node metastases and, in a few cases, liver metastases. The expression of HER2 and EGFR was scored from immunohistochemical preparations using the HercepTest criteria 0, 1+, 2+ or 3+ for cellular membrane staining while HER3 expression was scored as no, weak or strong cytoplasm staining. Material from 60 patients was analyzed. The number of EGFR 2+ or 3+ positive primary tumors was 16 out of 56 (29%) and for lymph node metastases 8 out of 56 (14%) whereas only one out of nine (11%) liver metastases were positive. Thus, there was lower EGFR positivity in the metastases. Only one among 53 patients was strongly HER2 positive and this in both the primary tumor and the metastasis. Eight out of 49 primary tumors (16%) were strongly HER3 positive and the corresponding numbers for lymph node metastases were 9 out of 49 (18%) and for liver metastases 2 out of 9 (22%). The observed number of strongly EGFR positive cases was somewhat low but EGFR might be, for the cases with high EGFR expression in metastases, a target for radionuclide therapy. HER2 seems not to be of such interest due to rare expression, neither HER3 due to mainly expression in the cytoplasm. The requirements for successful EGFR targeted radionuclide therapy are discussed, as well as patient inclusion criteria related to radionuclide therapy.
Insights
Epidermal growth factor receptor (EGFR) expression was lower in colorectal cancer metastases than primary tumors. EGFR may still be a target for radionuclide therapy in some metastatic cases, but HER2 and HER3 are less promising.
Area of Science:
- Oncology
- Radiochemistry
- Molecular Biology
Background:
- Epidermal growth factor receptor (EGFR) family members are potential targets for radionuclide therapy in EGFR-positive colorectal carcinomas (CRC), especially those resistant to existing EGFR inhibitors.
- Understanding the expression patterns of EGFR, HER2, and HER3 in primary CRC and its metastases is crucial for evaluating their suitability as therapeutic targets.
Purpose of the Study:
- To analyze the expression levels of EGFR, HER2, and HER3 in primary colorectal cancer tumors and their corresponding lymph node and liver metastases.
- To assess the potential of EGFR, HER2, and HER3 as targets for radionuclide therapy in colorectal cancer based on their expression profiles in primary and metastatic sites.
Main Methods:
- Immunohistochemical analysis was performed on samples from 60 colorectal cancer patients.
- EGFR and HER2 expression were scored using HercepTest criteria (0, 1+, 2+, 3+) for membrane staining.
- HER3 expression was scored for cytoplasmic staining (no, weak, strong).
Main Results:
- EGFR expression was lower in lymph node metastases (14%) and liver metastases (11%) compared to primary tumors (29%).
- Strong HER2 positivity was rare (1/53 patients).
- Strong HER3 positivity was observed in 16% of primary tumors, 18% of lymph node metastases, and 22% of liver metastases, primarily in the cytoplasm.
Conclusions:
- EGFR may serve as a target for radionuclide therapy in a subset of colorectal cancer patients with high EGFR expression in metastases.
- HER2 is unlikely to be a suitable target due to its rare expression.
- HER3 is less promising due to its predominantly cytoplasmic localization, which may limit its utility in targeted radionuclide therapy.
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