Evidence map›Paper›PMID 38727931›Full record

ArticleMolecular biology reports2024

Effects of CD44 siRNA on inhibition, survival, and apoptosis of breast cancer cell lines (MDA-MB-231 and 4T1).

Shaho Ghahremani Dehbokri, Saeed Noorolyai, Elham Baghbani, Nilofar Moghaddamneshat, Tohid Javaheri, Behzad Baradaran

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

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

6 authors.

Shaho Ghahremani DehbokriImmunology Research Center, Tabriz University of Medical Sciences, Daneshghah Ave, Tabriz, Iran.
Saeed NoorolyaiImmunology Research Center, Tabriz University of Medical Sciences, Daneshghah Ave, Tabriz, Iran.
Elham BaghbaniImmunology Research Center, Tabriz University of Medical Sciences, Daneshghah Ave, Tabriz, Iran.
Nilofar MoghaddamneshatDepartment of Biology, Faculty of Basic Science, Islamic Azad University of Center Tehran Branch, Tehran, Iran.
Tohid JavaheriYoung Researchers and Elites Club, Islamic Azad University, Mashhad Branch, Mashhad, Iran.
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Daneshghah Ave, Tabriz, Iran. baradaranb@tbzmed.ac.ir.ORCID http://orcid.org/0000-0002-8642-6795

Funding

Tabriz University of Medical Sciences, Tabriz, Iran Tabriz University of Medical Sciences, Tabriz, Iran
6 · The paper itself

Abstract

backgroundBreast cancer (BC) is one of the most common cancers in the world. Despite the many advances that have been made in treating patients, many patients are still resistant to treatment. CD44 is one of the surface glycoproteins of BC cells that plays an important role in the proliferation of these cells and inhibition of their apoptosis. Therefore, targeting it can be a treatment way for BC patients.

methodsIn this study, the effect of anti-CD44 siRNA on the proliferation, apoptosis, and migration rate of MDA-MB-231 and 4T1 cells was investigated. The techniques used in this study were MTT assay, RT-PCR, and flow cytometry.

resultsThe apoptosis and proliferation rates in CD44 siRNA-treated cells were higher and lower, respectively, compared to untreated cells. Also, cell migration was less in treated cells compared to untreated cells. CD44 siRNA also decreased the expression of CXCR4, c-myc, Vimentin, ROCK, and MMP-9.

conclusionFinally, CD44 targeting can be a good treatment option to make BC cells more sensitive to apoptosis.

Indexed as

ApoptosisBreast NeoplasmsHyaluronan ReceptorsRNA, Small InterferingCell Line, TumorCell MovementCell ProliferationCell SurvivalFemaleGene Expression Regulation, NeoplasticHumansMatrix Metalloproteinase 9Receptors, CXCR4VimentinCD44 protein, humanCXCR4 protein, humanHyaluronan ReceptorsMatrix Metalloproteinase 9Receptors, CXCR4RNA, Small InterferingVimentin4T1Breast cancerCD44MDA-MB-231siRNA

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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.