Evidence map›Paper›PMID 40636894›Full record

ArticleGalen medical journal2023

Characterization of Small Genetic Variants in Breast Cancer Cell Line Under Tamoxifen Therapy.

Mahnaz Nezamivand-Chegini, Hamed Kharrati-Koopaee, Seyed Taghi Heydari, Hasan Giahi, Fatemeh Sabahi, Ali Dehshahri, Kamran Bagheri Lankarani

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Article in Galen medical 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.

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5 · Who and what money

Authors and funding

7 authors.

Mahnaz Nezamivand-CheginiInstitute of Biotechnology, Shiraz University, Shiraz, Iran.
Hamed Kharrati-KoopaeeInstitute of Biotechnology, Shiraz University, Shiraz, Iran.
Seyed Taghi HeydariHealth Policy Research Center, Institute of Heath, Shiraz University of Medical Sciences, Shiraz, Iran.
Hasan GiahiInstitute of Biotechnology, Shiraz University, Shiraz, Iran.
Fatemeh SabahiDepartment of Plant Protection, College of Agriculture, Shiraz University, Shiraz, Iran.
Ali DehshahriDepartment of Pharmaceutical Biotechnology, Shiraz University of Medical Science, Shiraz, Iran.
Kamran Bagheri LankaraniHealth Policy Research Center, Institute of Heath, Shiraz University of Medical Sciences, Shiraz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTamoxifen (TAM) is an effective hormone therapy in order to reduce the risk of cancer recurrence. According to the available findings, TAM contributes to the alterations of genetic variants background and may have role in the effectiveness of treatments via alteration of the genetic variants. The effects of TAM on genomic features were investigated in current study through discovering genetic variants and finding the answer of the following question: "Is there any association between the alterations of genetic variants under TAM consumption and an effective treatment process?" MATERIALS AND

methodsWhole-transcriptome (RNA-seq) dataset of four investigations including 10 TAM-treated samples and 9 untreated samples as the control groups were derived from European Bioinformatics Institute (EBI). Using the process of variants calling, the differential genetic variants between and gene ontology enrichment analysis were detected through CLC Genomics Workbench (12).

resultsIn current study, almost 5.8 million genetic variants were reported. The outcomes of chi-square test showed that distributions of genetic variants between control and treated samples were significant (P0.05). The genetic variants comparison between the control and TAM-treated samples indicated that there were 67 differential genetic variants. Gene ontology enrichment analysis indicated that differential genetic variants were associated with several tumor suppressors and oncogenes such as IL6ST, GEN1, FNTA. HSPA5, NSMCE2, and DDX11.

conclusionMost of the candidate genes with differential genetic variants had dual roles as oncogenes or tumor suppressors. Therefore, it can be claimed that TAM has no significant role in an effective treatment through alteration of the genetic variants. In other words, it cannot be concluded that the TAM therapy-resulted alterations of genetic variants have positive or negative roles in the treatment process.

Indexed as

Breast NeoplasmsRNA-seqTamoxifen

Identifiers

PMID40636894
PMCPMC12070920

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