Frequently increased epidermal growth factor receptor (EGFR) copy numbers and decreased BRCA1 mRNA expression in Japanese triple-negative breast cancers
2008

Increased EGFR and Decreased BRCA1 in Japanese Triple-Negative Breast Cancers

Sample size: 969 publication 10 minutes Evidence: moderate

Author Information

Author(s): Toyama Tatsuya, Yamashita Hiroko, Kondo Naoto, Okuda Katsuhiro, Takahashi Satoru, Sasaki Hidefumi, Sugiura Hiroshi, Iwase Hirotaka, Fujii Yoshitaka

Primary Institution: Nagoya City University Graduate School of Medical Sciences

Hypothesis

Are EGFR copy numbers increased and BRCA1 mRNA expression decreased in Japanese triple-negative breast cancers?

Conclusion

Triple-negative breast cancers have an aggressive clinical course, and EGFR and BRCA1 might be candidate therapeutic targets in this disease.

Supporting Evidence

  • 11.3% of patients had triple-negative breast cancers.
  • 21% of triple-negative breast cancers showed increased EGFR gene copy numbers.
  • BRCA1 mRNA expression was significantly lower in triple-negative breast cancers compared to controls.
  • Triple-negative status was associated with grade 3 tumors and high Ki67 expression.

Takeaway

This study looked at breast cancer in Japanese patients and found that a type called triple-negative breast cancer often has more copies of a gene called EGFR and less of another gene called BRCA1, which could help doctors find new treatments.

Methodology

The study analyzed 969 patients diagnosed with invasive breast cancer, focusing on immunohistochemical data and gene expression using TaqMan PCR assays.

Potential Biases

Potential biases may arise from the retrospective nature of the study and the selection of patients from a single institution.

Limitations

The study did not analyze BRCA1 gene mutations and relied on historical data from patients treated over a long period.

Participant Demographics

The study involved 969 Japanese patients diagnosed with invasive breast cancer.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1471-2407-8-309

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