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Updated: Jan 29, 2026

Studying the Stoichiometry of Epidermal Growth Factor Receptor in Intact Cells using Correlative Microscopy
Published on: September 11, 2015
Targeting Epidermal Growth Factor Receptor (EGFR) and Human Epidermal Growth Factor Receptor 2 (HER2) Expressing
Mohammad R Siddiqui1,2, Reema Railkar1, Thomas Sanford1
1Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD - 20892, USA.
Abstract:
Bladder cancer (BC) is heterogeneous and expresses various cell surface targets. Photoimmunotherapy (PIT) involves monoclonal antibodies (MAbs) conjugated to a photoabsorber (PA), IR Dye 700Dx, and then activated by near infra-red light (NIR) to specifically target tumors. We have demonstrated that tumors expressing EGFR can be targeted with PIT. However, PIT may be less effective when a tumor lacks "overwhelming" expression of a single target such as EGFR. We present a combinatorial PIT approach for targeting BC expressing EGFR and HER2, using PA- labeled panitumumab (pan) and trastuzumab (tra), respectively. Human BC tissues and cell lines were analyzed for EGFR and HER2 expression. Efficacy of PA-labeled MAbs singly and in combination was analyzed. About 45% of BC tissues stain for both EGFR and HER2. In vitro, the combination of pan IR700 and tra IR700 with NIR was more efficacious than either agent alone. Tumor xenografts treated with combination PIT showed significant tumor growth retardation. Combination PIT is a promising approach for treating BC with low/moderate expression of surface receptors. In addition, given the molecular heterogeneity of bladder cancer, targeting more than one surface receptor may allow for more effective cell death across different bladder tumors.
Insights
This study introduces a combination photoimmunotherapy (PIT) approach for bladder cancer (BC) targeting both EGFR and HER2. This combinatorial therapy shows improved efficacy over single-target treatments, offering a promising strategy for heterogeneous BC.
Area of Science:
- Oncology
- Immunotherapy
- Biotechnology
Background:
- Bladder cancer (BC) is molecularly heterogeneous, expressing diverse cell surface targets.
- Photoimmunotherapy (PIT) utilizes antibody-photoabsorber conjugates activated by near-infrared light (NIR) for targeted tumor destruction.
- Current PIT efficacy may be limited in tumors with low or heterogeneous target expression.
Purpose of the Study:
- To evaluate a combinatorial PIT strategy for bladder cancer targeting both EGFR and HER2.
- To assess the efficacy of combining panitumumab-IR700 and trastuzumab-IR700 in preclinical models of BC.
- To investigate the potential of dual-receptor targeting for overcoming limitations of single-target PIT.
Main Methods:
- Analysis of EGFR and HER2 expression in human BC tissues and cell lines.
- In vitro efficacy assessment of single and combination PA-labeled MAb treatments with NIR activation.
- In vivo evaluation of combination PIT efficacy in BC tumor xenografts.
Main Results:
- Approximately 45% of BC tissues co-expressed EGFR and HER2.
- Combination therapy (panitumumab-IR700 + trastuzumab-IR700 + NIR) demonstrated superior in vitro efficacy compared to individual agents.
- Combination PIT significantly inhibited tumor growth in xenograft models.
Conclusions:
- Combinatorial PIT targeting EGFR and HER2 is effective for bladder cancer, particularly in tumors with low or moderate receptor expression.
- Dual-receptor targeting enhances cell death and offers a more robust therapeutic approach for molecularly diverse bladder tumors.
- This strategy holds promise for improving treatment outcomes in heterogeneous bladder cancer.
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