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pmid:35368753

Development of a Model System to Study Expression Profile of RAC2 Gene in Breast Cancer MDA-MB-231 Cell Line.

Thogulva Sivakumar Harish · Polani Ramesh Babu · Anupama Shrestha · Balamuralikrishnan Balasubramanian · Arunachalam Chinnathambi · Sulaiman Ali Alharbi

Evidence-based complementary and alternative medicine : eCAM · 2022 doi:10.1155/2022/2077850

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Development of a Model System to Study Expression Profile of RAC2 Gene in Breast Cancer MDA-MB-231 Cell Line.
doi
10.1155/2022/2077850
pmid
35368753
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Thogulva Sivakumar Harish
[1]
Polani Ramesh Babu
[2]
Anupama Shrestha
[3]
Balamuralikrishnan Balasubramanian
[4]
Arunachalam Chinnathambi
[5]
Sulaiman Ali Alharbi
journal
Evidence-based complementary and alternative medicine : eCAM
year
2022
abstract
The RAC2 gene encoding GTPases involve cellular signaling of actin polymerization, cell migration, and formation of the phagocytic NADPH oxidase complex. Oncogenic mutations in the RAC2 gene have been identified in various cancers, and extensive research is in progress to delineate its signaling pathways and identify potential therapeutic targets in breast cancers. This paper explored developing a bioinformatics model system to understand the RAC2 gene expression pattern concerning estrogenic receptor status in breast cancers. We have used the MDA-MB-231 breast cancer cell line to identify RAC2 gene expression. To simplify the development of model system with one dataset, we retrieved the microarray dataset GSE27515 from the Gene Expression Omnibus (GEO) for the differential gene expression analysis. Then, network analysis, pathway enrichment analysis, volcano plot, ORA, and the up/downregulated genes were used to highlight genes involved in signaling network pathways. We observed that the RAC2 gene is upregulated in the GSM679722, GSM676923, and GSM679724 downregulated in the samples GSM676925, GSM676926, and GSM676927 from the GEO dataset. Our observation found that the RAC2 gene is upregulated in the estrogen receptor (ER) negative breast cancers and downregulated in ER-positive breast cancer, involving pathways such as focal adhesion, MAPK signaling, axon guidance, and VEGF signaling pathway.
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Isolation and characterization of a metastatic hybrid cell line generated by ER negative and ER positive breast cancer cells in mouse bone marrow
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