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pmid:24982892

Computational analysis of mRNA expression profiles identifies the ITG family and PIK3R3 as crucial genes for regulating triple negative breast cancer cell migration.

Sukhontip Klahan · Mei-Shin Wu · Edward Hsi · Chi-Cheng Huang · Ming-Feng Hou · Wei-Chiao Chang

BioMed research international · 2014 doi:10.1155/2014/536591

Paper

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Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:24982892
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science-record
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2026-11-01T15:40:05Z
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paper object · 10 fields
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title
Computational analysis of mRNA expression profiles identifies the ITG family and PIK3R3 as crucial genes for regulating triple negative breast cancer cell migration.
doi
10.1155/2014/536591
pmid
24982892
authors array · 6 items
[0]
Sukhontip Klahan
[1]
Mei-Shin Wu
[2]
Edward Hsi
[3]
Chi-Cheng Huang
[4]
Ming-Feng Hou
[5]
Wei-Chiao Chang
journal
BioMed research international
year
2014
abstract
Triple-negative breast cancer (TNBC) is an aggressive type of breast cancer that does not express estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor (Her2/neu). TNBC has worse clinical outcomes than other breast cancer subtypes. However, the key molecules and mechanisms of TNBC migration remain unclear. In this study, we compared two normalized microarray datasets from GEO database between Asian (GSE33926) and non-Asian populations (GSE46581) to determine the molecules and common pathways in TNBC migration. We demonstrated that 16 genes in non-Asian samples and 9 genes in Asian samples are related to TNBC migration. In addition, our analytic results showed that 4 genes, PIK3R3, ITGB1, ITGAL, and ITGA6, were involved in the regulation of actin cytoskeleton. Our results indicated potential genes that link to TNBC migration. This study may help identify novel therapeutic targets for drug development in cancer therapy.
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Gene expression profile calculations were conducted using SAM method [22] and R (vers. 2.15.1).
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sections[5] "2.3. Gene Expression Calculations" paragraph 2
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Gene expression profile calculations were conducted using SAM method [22] and R (vers. 2.15.1).
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These two datasets were deposited in the GEO database under the respective codes GSE46581 and GSE33926. Data of GSE46581 were generated by Illumina HumanRef-8 WG-DASL v3.0 (GPL8432), a Whole-Genome DASL Assay which simultaneously analyzes over 24,000 genes with high sensitivity [19].
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sections[3] "2.1. Data Resources" paragraph 2
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These two datasets were deposited in the GEO database under the respective codes GSE46581 and GSE33926. Data of GSE46581 were generated by Illumina HumanRef-8 WG-DASL v3.0 (GPL8432), a Whole-Genome DASL Assay which simultaneously analyzes over 24,000 genes with high sensitivity [19].
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Using Significance Analysis of Microarrays on two normalized GEO microarray datasets, the study identified 16 migration-related genes in non-Asian TNBC samples and 9 in Asian samples.
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Molecular characteristics and metastasis predictor genes of triple-negative breast cancer
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Yale Triple Negative Breast Cancer Cohort
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Common genes between Asian and non-Asian populations.
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25 migration related genes in Asian and non-Asian populations.
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3.3. Pathway Analysis of TNBC from Non-Asian and Asian Patients
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Migration related gene network in Asian and non-Asian populations.
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3.3. Pathway Analysis of TNBC from Non-Asian and Asian Patients
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TNBC has worse clinical outcomes than other breast cancer subtypes. However, the key molecules and mechanisms of TNBC migration remain unclear. In this study, we compared two normalized microarray datasets from GEO database between Asian (GSE33926) and non-Asian populations (GSE46581) to determine the molecules and common pathways in TNBC migration. We demonstrated that 16 genes in non-Asian samples and 9 genes in Asian samples are related to TNBC migration. In addition, our analytic results showed that 4 genes, PIK3R3, ITGB1, ITGAL, and ITGA6, were involved in the regulation of actin cytoskeleton. Our results indicated potential genes that link to TNBC migration. 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