Evidence map›Paper›PMID 38019229›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2023

Metformin Caused Radiosensitivity of Breast Cancer Cells through the Expression Modulation of miR-21-5p/SESN1axis.

Fatemeh Saffari, Abdoalmabood Momeni, Mehrzad Ramezani, Yasamin Ansari, Sahar Moghbelinejad

Abstract read
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Article in Asian Pacific journal of cancer prevention : APJCP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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.

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Fatemeh SaffariChildren Growth Research Center, Research Institute for Prevention of Non-Communicable disease, Qazvin University of Medical Science, Qazvin,Iran.
Abdoalmabood MomeniKhatam Pathobiology and Genetic Lab, Qazvin, Iran.
Mehrzad RamezaniKhatam Pathobiology and Genetic Lab, Qazvin, Iran.
Yasamin AnsariDepartement of Medicine, Zanjan University Of Medical Science, Zanjan, Iran.
Sahar MoghbelinejadCellular and Molecular Research Centre, Research Institute for Prevention of Non-Communicable Diseases, Qazvin University of Medical Sciences, Qazvin, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn this research we evaluated molecular mechanism of effect of metformin in radio sensitivity of breast cancer cells.

methodsThis research was done in cellular and molecular research center of Qazvin university of Medical science in 1399 to 1401. Studied samples were two breast cancer cell lines (MCF-7 and MDA-MB-231) they are derived from primary and secondary tumors resected from a single patient. We exposed them to cumulative 50 Gy radiation and constructed radio resistant cell lines. Then resistant cell lines were treated with 50µm of metformin. Our studied groups were resistant cells treated and un treated with metformin. Then, the expression rate of miR-21-5p and SESN1 gene in resistant and control cells was checked by Quantitative Real-time PCR(qRTPCR). After the cell lines were treated with different concentrations of metformin at different intervals, the rate of cell proliferation and cell death was checked by CCK-8 assay and flow cytometry. The Western blot method was also used to confirm the expression of some genes.

resultsOur results showed that the expression of miR-21-5p was upregulated in radiation-resistant cancer cells (1.8±0.65) (P<0.0001) MCF-7 cell line and (1.6±0.42)(P<0.001) MBA-MD-231 cell line, while the expression of SESN1 was down regulated (0.46±0.12) (P<0.0001) MCF-7 cell line and (0.42±0.22) (P<0.001) MBA-MD-231 cell line. Metformin enhanced the radio sensitivity of breast cancer cells in a dose and time-dependent manner. Also, metformin treatment decreased the expression of miR-21-5p (0.47±0.32) (P<0.0001) MCF-7 Cell line and (0.45±0.21)(P<0.001) MBA-MD-231 cell line and increased the expression of SESN1 (1.65±0.72)(P<0.0001)MCF-7 cell line and (1.73±0.52)(P<0.0001) MBA-MD-231 cell line. The function of metformin was reversed by miR-21-5p inhibitors or the transfection of SESN1 overexpressing plasmids.

conclusionIn conclusion, based on this research results, metformin enhanced the radio sensitivity of breast cancer cells via modulating  the expression of miR-21-5p and SESN1.

Indexed as

Breast NeoplasmsMetforminMicroRNAsSestrinsFemaleHumansMCF-7 CellsRadiation ToleranceTranscription FactorsMetforminMicroRNAsMIRN21 microRNA, humanSESN1 protein, humanSestrinsTranscription Factorsbreast cancerMetforminmiR-21-5pRadio resistantSESN1 gene

Identifiers

PMID38019229
PMCPMC10772753

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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.