Evidence map›Paper›PMID 41455890›Full record

ArticleBMC immunology2025

Investigating monoclonal antibody against cytokeratin 19 tumor marker.

Mohammad Amin Momeni-Moghaddam, Javad Mohammadnejad, Hossein Ghahremani, Shahnaz Khaghani, Nariman Moradi, Amin Daemi, Gülüzar Özbolat, Yusuf Döğüş, Seyyedeh Touran Hosseini

Abstract read
In one paragraph

Article in BMC immunology, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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

9 authors.

Mohammad Amin Momeni-MoghaddamDepartment of Nutrition and Biochemistry, Gonabad University of Medical Sciences, Gonabad, Iran.
Javad MohammadnejadDepartment of Nanobiotechnology and Biomimetic, School of Life Science Engineering, College of interdisciplinary Science and Technology, University of Tehran, Tehran, Iran.
Hossein GhahremaniDepartment of Biochemistry, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Shahnaz KhaghaniDepartment of Biochemistry, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Nariman MoradiCellular and Molecular Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Amin DaemiDepartment of Medical Biochemistry, Faculty of Medicine, Cukurova University, Adana, Turkey. phd_bio@yahoo.com.
Gülüzar ÖzbolatFaculty of Health Science, Sinop University, Sinop, Turkey.
Yusuf DöğüşDepartment of Medical Biochemistry, Faculty of Medicine, Cukurova University, Adana, Turkey.
Seyyedeh Touran HosseiniDepartment of Biotechnology, Institute of Natural and Applied Sciences, Cukurova University, Adana, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokeratin 19 (CK 19) is a member of the intermediate filaments that are widely expressed in thyroid, breast, colon, small and non-small cell lung, and prostate cancer cells. This paper aims to produce the monoclonal antibody against CK 19. Recombinant CK 19 was used to immunize of two 6–8 weeks old female Balb/c mice. For the first injection, recombinant antigen was mixed with the complete Freund′s Adjuvant, and for the second and third injections, mixed with the Incomplete Freund′s Adjuvant. Injections were performed at intervals of 15 days. Four days after the third injection, titration of mice serum was determined using indirect ELISA and better-immunized mice selected for fusion. Intravenous (IV) injection was performed 4 days before the fusion. The spleen cells of the mice were fused with sp2/0 cells using 50% v/v polyethylene glycol (PEG) and cells were suspended in HAT (Hypoxanthine-Aminopterin-Thymidine) medium. Supernatants of hybridoma cells were screened for antibody secretion by indirect ELISA. Two stable hybridomas were obtained among 78 hybridoma clones that reacted with the recombinant CK 19 by indirect ELISA. These hybridoma cells were monoclonal twice by limiting dilution. Besides, immunization by recombinant CK 19 led to the obtaining of two stable monoclonal antibodies against this antigen. Western blotting with HT-29 cell line demonstrated a band of upper than 43 kDa. Result of HepG2 indicated a band of lower than 45 kDa while MCF7 bands of 45 kDa and higher were observed for MCF7. A431 cell line was epidermoid carcinoma, as CK 19 did not exist in the epidermis, therefore no band was observed in A431 cell line.

Indexed as

Antibodies, MonoclonalBiomarkers, TumorKeratin-19AnimalsAntibody SpecificityCell Line, TumorEnzyme-Linked Immunosorbent AssayFemaleHT29 CellsHumansHybridomasImmunizationMiceMice, Inbred BALB CRecombinant ProteinsAntibodies, MonoclonalBiomarkers, TumorKeratin-19Recombinant ProteinsCK19Monoclonal antibodyTumor marker

Identifiers

PMID41455890
PMCPMC12860061

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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.