Evidence map›Paper›PMID 37070675›Full record

ArticleIranian biomedical journal2023

K-Ras4A Plays a More Significant Role than K-Ras4B in Ductal Carcinoma of Breast.

Mohamad Mahdi Mortazavipour, Zeinab Mohamadalizadeh-Hanjani, Loabat Geranpayeh, Reza Mahdian, Shirin Shahbazi

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Article in Iranian biomedical journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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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0 citing papers in PubMed, 0 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Mohamad Mahdi MortazavipourDepartment of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, ‎Tehran, Iran.
Zeinab Mohamadalizadeh-HanjaniDepartment of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, ‎Tehran, Iran.
Loabat GeranpayehDepartment of Surgery, Sina Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Reza MahdianMolecular Medicine Department, Pasteur Institute of Iran, Tehran, Iran.
Shirin ShahbaziDepartment of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, ‎Tehran, Iran.
Tarbiat Modares University · IRPasteur Institute of Iran · IRSina Hospital · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: K-Ras mutations rarely occur in breast cancer. However, studies have supported that K-Ras upregulation is involved in breast cancer pathogenesis. Two main K-Ras transcript variants; K-Ras4A and K-Ras4B, originate from the alternative splicing of exon 4. In this study, we aimed to evaluate variations in the expression of K-Ras4A and K-Ras4B and their role in breast ductal carcinoma. Methods: Total RNA was extracted from breast tumors, and the NATs obtained via mastectomy. Patients were selected from new cases of breast cancer with no prior history of chemotherapy. Relative mRNA expression was calculated based on a pairwise comparison between the tumors and the NATs following normalization to the internal control gene. Predictive values of the transcript variants were examined by ROC curve analysis. Results: A statistically significant increase was found in the K-Ras4A and K-Ras4B expression with the mean fold changes of 7.58 (p = 0.01) and 2.47 (p = 0.001), respectively. The K-Ras4A/K-Ras4B ratio was lower in the tumors than that of the normal tissues. ROC curve analysis revealed the potential of K-Ras4A (AUC: 0.769) and K-Ras4B (AUC: 0.688) in breast cancer prediction. There was also a significant association between K-Ras4B expression and HER2 statues (p = 0.04). Furthermore, a significant link was detected between K-Ras4A expression and pathological prognostic stages (p = 0.04). Conclusion: Our findings revealed that expression levels of K-Ras4A and K-Ras4B is higher in the tumor compared to the normal breast tissues. Increase in K-Ras4A expression was more significant than that of K-Ras4B.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastAlternative SplicingFemaleHumansMastectomyAlternative splicingBreast neoplasmsGene expressionKRAS proteinReal-time polymerase chain reaction

Identifiers

PMID37070675
PMCPMC10314762
OpenAlexW4366235889

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