Cytoplasmic CXCR4 expression in breast cancer: induction by nitric oxide and correlation with lymph node metastasis and poor prognosis
2008

CXCR4 in Breast Cancer: Role of Nitric Oxide and Prognosis

Sample size: 113 publication 10 minutes Evidence: moderate

Author Information

Author(s): Yasuoka Hironao, Tsujimoto Masahiko, Yoshidome Katsuhide, Nakahara Masaaki, Kodama Rieko, Sanke Tokio, Nakamura Yasushi

Primary Institution: Wakayama Medical University

Hypothesis

Does nitric oxide induce CXCR4 expression and correlate with lymph node metastasis in breast cancer?

Conclusion

Cytoplasmic CXCR4 expression is significantly associated with lymph node metastasis and poor prognosis in breast cancer.

Supporting Evidence

  • Cytoplasmic CXCR4 expression was observed in 50% of tumors.
  • High nitrotyrosine levels correlated with lymph node metastasis (p < 0.001).
  • Kaplan-Meier survival curves indicated reduced survival associated with cytoplasmic CXCR4 expression.
  • Multivariate analysis identified cytoplasmic CXCR4 as an independent predictor for survival.
  • NO donor treatment increased CXCR4 expression in breast cancer cell lines.

Takeaway

This study found that a substance called nitric oxide can make a protein called CXCR4 more active in breast cancer cells, which may help the cancer spread and make it harder for patients to survive.

Methodology

CXCR4 expression was analyzed in breast cancer tissues and cell lines, with assessments of nitrotyrosine levels and survival analysis conducted.

Potential Biases

Potential bias in immunostaining interpretation as it was performed by pathologists without clinical knowledge of the patients.

Limitations

The study is based on archival specimens and may not account for all variables affecting CXCR4 expression.

Participant Demographics

Median age of participants was 51 years, with 58% younger than 50 and 52% having lymph node metastasis.

Statistical Information

P-Value

p = 0.0002 for overall survival

Confidence Interval

Not provided

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1471-2407-8-340

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