# Identification of Common Cancer Antigens Useful for Specific Immunotherapies to Colorectal Cancer and Liver Metastases

**Authors:** Jun Kataoka, Kazumasa Takenouchi, Toshihiro Suzuki, Kazunobu Ohnuki, Yuichiro Tsukada, Naoto Gotohda, Masaaki Ito, Tetsuya Nakatsura

PMC · DOI: 10.3390/ijms26157402 · 2025-07-31

## TL;DR

This study identifies cancer antigens in colorectal cancer and liver metastases that could be targeted for immunotherapies.

## Contribution

The study identifies specific cancer antigens and HLA class I expression patterns for immunotherapy targeting in colorectal cancer and liver metastases.

## Key findings

- CLDN1, EphB4, and LAT1 are highly expressed in both colorectal cancer and liver metastases.
- HLA class I is expressed on the cell membrane in 80% of primary tumors.
- FOXM1 and SPARC expression is lower in liver metastases compared to primary tumors.

## Abstract

Stage IV colorectal cancer has a poor prognosis, and liver metastases are prone to recurrence, even after resection. This study aimed to identify common cancer antigens, using immunohistochemical staining, as promising targets for antigen-specific immunotherapies in colorectal cancer. We analyzed expression levels and intracellular localization of seven common cancer antigens, CLDN1, EphB4, LAT1, FOXM1, HSP105α, ROBO1, and SPARC, and human leukocyte antigen (HLA) class I via immunohistochemical staining of 85 surgical specimens from primaries and liver metastases. Staining intensity and positive staining were scored to evaluate antigen expression. In 25 primaries, seven cancer antigens were expressed in 88–96% of cases, while HLA class I was expressed on the cell membrane in 80.0% of cases. In 60 liver metastases, FOXM1 and SPARC expression were approximately half that observed in the primaries. Other antigens and HLA class I were highly expressed in both. Most of the primaries and liver metastases may benefit from chimeric antigen receptor-T cell therapy targeting CLDN1, EphB4, and LAT1. Cases with high HLA class I expression may be suitable for vaccine-based and T cell receptor-T cell therapy targeting CLDN1, EphB4, LAT1, FOXM1, HSP105α, ROBO1, and SPARC for primaries and targeting antigens, excluding FOXM1 and SPARC, for liver metastases.

## Linked entities

- **Genes:** CLDN1 (claudin 1) [NCBI Gene 9076], EPHB4 (EPH receptor B4) [NCBI Gene 2050], SLC7A5 (solute carrier family 7 member 5) [NCBI Gene 8140], FOXM1 (forkhead box M1) [NCBI Gene 2305], HSPH1 (heat shock protein family H (Hsp110) member 1) [NCBI Gene 10808], ROBO1 (roundabout guidance receptor 1) [NCBI Gene 6091], SPARC (secreted protein acidic and cysteine rich) [NCBI Gene 6678]
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** EPHB4 (EPH receptor B4) [NCBI Gene 2050] {aka CMAVM2, HFASD, HTK, LMPHM7, MYK1, TYRO11}, SPARC (secreted protein acidic and cysteine rich) [NCBI Gene 6678] {aka BM-40, OI17, ON, ONT}, ROBO1 (roundabout guidance receptor 1) [NCBI Gene 6091] {aka CPHD8, DUTT1, NORS, NYS8, SAX3}, FOXM1 (forkhead box M1) [NCBI Gene 2305] {aka FKHL16, FOXM1A, FOXM1B, FOXM1C, HFH-11, HFH11}, HSPH1 (heat shock protein family H (Hsp110) member 1) [NCBI Gene 10808] {aka HSP105, HSP105A, HSP105B, NY-CO-25}, SLC7A5 (solute carrier family 7 member 5) [NCBI Gene 8140] {aka 4F2LC, CD98, D16S469E, E16, LAT1, MPE16}, CLDN1 (claudin 1) [NCBI Gene 9076] {aka CLD1, ILVASC, SEMP1}
- **Diseases:** Colorectal Cancer (MESH:D015179), Liver Metastases (MESH:D009362), Cancer (MESH:D009369)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12347713/full.md

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Source: https://tomesphere.com/paper/PMC12347713