Evidence map›Paper›PMID 41663855›Full record

ArticleThe protein journal2026

Preparation and Evaluation of a Multi-Epitope Peptide for Assessing Immunotherapy of Colorectal Cancer in Vivo.

Fatemeh Bahramibanan, Meysam Soleimani, Amir Taherkhani, Hamidreza Ghadimipour, Rezvan Najafi, Nastaran Barati, Katayoun Derakhshandeh

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Article in The protein journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Fatemeh BahramibananResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Meysam SoleimaniDepartment of Pharmaceutics, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran. meysambadia@gmail.com.
Amir TaherkhaniResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Hamidreza GhadimipourDepartment of Pathology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Rezvan NajafiResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Nastaran BaratiDepartment of Pharmaceutics, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.
Katayoun DerakhshandehDepartment of Pharmaceutics, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of tumor heterogeneity is a critical issue that restricts the success of targeted therapies and negatively impacts patient outcomes. Recent studies have concentrated on the development of multi-epitope peptides that exhibit considerable overexpression in cancerous tissues with the aim of activating immune cells and utilizing immune-mediated responses to effectively suppress tumor growth. In this study, genes with increased expression in colorectal cancer (CRC) were identified using GEO data and R software. Following overexpression confirmation of APCDD1, we identified epitopes from the protein that can be recognized by various MHC molecules and presented on APC cell surfaces. Subsequent to expression and purification of the multi-epitope peptide and investigation on the BALB/c mice harboring tumor xenograft, obtained results showed a significant reduction in tumor growth, mitotic cell count, angiogenesis, metastasis, and an increase in Tumor-Infiltrating Lymphocytes (TILs) in the tumor microenvironment. Overall, the finding highlight the potential of multi-epitope peptide in CRC immunotherapy, where it may address the significant challenge of tumor heterogeneity.

Indexed as

Colorectal NeoplasmsEpitopesImmunotherapyPeptidesAnimalsCell Line, TumorHumansLymphocytes, Tumor-InfiltratingMiceMice, Inbred BALB CTumor MicroenvironmentEpitopesPeptidesColorectal cancerImmunotherapyMHC II receptorMHC I receptorMulti-epitope peptideRecombinant peptide

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.