Identification of novel diagnostic biomarkers in stages I-IV colorectal cancer

Abstract Background Additional new biomarkers that aid in detecting colorectal adenocarcinoma early are definitely needed. Here, we report that tumor-specific CDX2, CD74, HER2, CD104, and CD26 genes are differentially expressed in the tumor microenvironment (stages I-IV) in patients with colorectal cancer. Material and methods Tumor CDX2, CD74, HER2, CD26 , and CD104 expression levels were studied by immunohistochemistry and RT-qPCR. Tissues from 210 patients with CRC (stages I–IV) were used. Additionally, gene expression ( CDX2, CD74, HER2, CD26, and CD104 ) of CRC patients, CRC with metastasis, and normal tissues were identified using 4 GEO datasets. Results At the mRNA and protein levels, CDX2 was more highly expressed in tumor tissue (I–IV) than in surrounding normal tissue ( P < 0.0001). Furthermore, the ROC curve analysis demonstrated that CDX2 can be a suitable biomarker at all stages. CD74 and CD104 showed a significant increase in expression. However, CD26 did not show any significant increase in mRNA and protein expression. The results of the GEOR2 analyses also confirmed the present results. Conclusions This proof-of-principle study demonstrated that CDX2 is a biomarker for diagnosis and prognosis strategies for CRC. On the other hand, CD74 and CD104 are recommended for diagnosis in stages I and II. The results justify prospective validation to clarify the clinical impact of these biomarkers in cancer diagnosis.

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Publication Details

Journal
Egyptian Journal of Medical Human Genetics
Published
2025-04-22
DOI
https://doi.org/10.1186/s43042-025-00716-5
Citations
2
Primary Topic
Genetic factors in colorectal cancer
Type
article
Field-Weighted Citation Impact
2.94

Funders

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article

Identification of novel diagnostic biomarkers in stages I-IV colorectal cancer

Ali Ghorbani Ranjbary, Mohammadreza Azimi, Seyed Sina Sabbaghi, Sarvin Alizadeh Sadighi et al.
2 citations
Egyptian Journal of Medical Human Genetics
Genetic factors in colorectal cancer
2.94
article

Identification of novel diagnostic biomarkers in stages I-IV colorectal cancer

Ali Ghorbani Ranjbary, Mohammadreza Azimi, Seyed Sina Sabbaghi, Sarvin Alizadeh Sadighi, Vesal Abbasian
article en
2 citations

Abstract

Abstract Background Additional new biomarkers that aid in detecting colorectal adenocarcinoma early are definitely needed. Here, we report that tumor-specific CDX2, CD74, HER2, CD104, and CD26 genes are differentially expressed in the tumor microenvironment (stages I-IV) in patients with colorectal cancer. Material and methods Tumor CDX2, CD74, HER2, CD26 , and CD104 expression levels were studied by immunohistochemistry and RT-qPCR. Tissues from 210 patients with CRC (stages I–IV) were used. Additionally, gene expression ( CDX2, CD74, HER2, CD26, and CD104 ) of CRC patients, CRC with metastasis, and normal tissues were identified using 4 GEO datasets. Results At the mRNA and protein levels, CDX2 was more highly expressed in tumor tissue (I–IV) than in surrounding normal tissue ( P < 0.0001). Furthermore, the ROC curve analysis demonstrated that CDX2 can be a suitable biomarker at all stages. CD74 and CD104 showed a significant increase in expression. However, CD26 did not show any significant increase in mRNA and protein expression. The results of the GEOR2 analyses also confirmed the present results. Conclusions This proof-of-principle study demonstrated that CDX2 is a biomarker for diagnosis and prognosis strategies for CRC. On the other hand, CD74 and CD104 are recommended for diagnosis in stages I and II. The results justify prospective validation to clarify the clinical impact of these biomarkers in cancer diagnosis.

Egyptian Journal of Medical Human GeneticsVol. 26(1)
Islamic Azad University of Garmsar (IR), University of Tehran (IR), Islamic Azad University Saveh (IR), Shahid Beheshti University of Medical Sciences (IR), Ferdowsi University of Mashhad (IR)
Ferdowsi University of Mashhad, University of Tehran
Openalex Percentile: Top 10%
Genetic factors in colorectal cancer
2.94
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