Evidence map›Paper›PMID 39916422›Full record

ArticleRecent patents on biotechnology2025

Development of a Novel Peptide with RGD Tumor Homing Motif: Evaluation of its Anticancer Potential in Hepatocellular Carcinoma and Colon Cancer Cells.

Reda Abdallah Mohamed, Ohoud Mohammed Marie, Dahlia Ibrahim Badran, Olfat Ali Hammam, Hend Okasha Ahmed

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Article in Recent patents on biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Reda Abdallah MohamedDepartment of Chemistry, Faculty of Science, Suez Canal University, Ismailia, Egypt.
Ohoud Mohammed MarieDepartment of Chemistry, Faculty of Science, Suez Canal University, Ismailia, Egypt.ORCID 0000-0003-2846-8476
Dahlia Ibrahim BadranDepartment of Medical Biochemistry, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Olfat Ali HammamDepartment of Pathology, Theodor Bilharz Research Institute, Giza, Egypt.ORCID 0000-0002-4965-5804
Hend Okasha AhmedDepartment of Biochemistry and Molecular Biology, Theodor Bilharz Research Institute, Giza, Egypt.ORCID 0000-0003-1125-245X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeptide-based therapy has emerged as a promising avenue for treating various disorders, and recent research has highlighted the potential of anti-cancer peptides (ACPs) in cancer treatment. In this context, this study aimed to design a novel peptide incorporating a tumor-homing peptide (RGD) and C-amidation to enhance its anticancer activity, particularly against liver (HepG2) and colon (HCT-116) cancer cell lines.

objectivesThe primary objective was to design a peptide with improved anticancer properties by leveraging the tumor-homing capabilities of RGD and enhancing its activity through C-amidation. The study sought to evaluate the cytotoxicity of the designed peptide against red blood cells (RBCs) and normal Vero cells. Furthermore, the anticancer efficacy of the peptide was assessed in hepatocellular carcinoma (HepG2) and colon cancer (HCT-116) cell lines. The specific objectives included examining the apoptotic induction and morphological changes in treated cells compared to untreated cells.

methodsThe peptide was designed using the ACPred-FL bioinformatics tool, and its cytotoxicity was assessed through hemolysis assays against RBCs and normal Vero cells. Anticancer activity was evaluated against HepG2 and HCT-116 cell lines. The analysis of apoptotic induction involved measuring the relative gene expression of oncogenic marker BCL2 and apoptotic markers (BAX, BID, CAS-8). Additionally, Cytopathological examination and Western Blot analysis were employed to study morphological changes and confirm the quantification of relevant markers.

resultsThe designed peptide, consisting of twelve amino acids with a molecular mass of 1230.6233 Da and an isoelectric point of 9.81, exhibited low erythrocyte lysis and minimal toxicity to normal cells. The IC

conclusionThe designed peptide is considered a patent product that displayed remarkable anticancer activity against hepatocellular carcinoma and colon cancer cell lines, effectively modulating apoptotic and oncogenic markers. These findings highlight the potential of the peptide as a therapeutic agent for cancer treatment, emphasizing its clinical significance in combating liver and colon cancers. Nonetheless, further research and development are warranted to explore the translational potential of this peptide in clinical studies.

Indexed as

Antineoplastic AgentsCarcinoma, HepatocellularColonic NeoplasmsLiver NeoplasmsOligopeptidesPeptidesAnimalsApoptosisChlorocebus aethiopsErythrocytesHCT116 CellsHemolysisHep G2 CellsHumansVero CellsAntineoplastic Agentsarginyl-glycyl-aspartic acidOligopeptidesPeptidesACPs.apoptosiscolon cancerhepatocellular carcinomaPeptidetumor homing peptide

Identifiers

PMID39916422

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