AI Article Synopsis

  • A study analyzed 300 triple-negative breast cancer (TNBC) samples and 120 paired non-cancerous tissues to assess the roles of MAPK and EGFR in disease progression.
  • Results showed that MAPK and EGFR levels were significantly higher in TNBC tissues compared to paracancerous tissues and that their expressions were correlated.
  • Higher expression rates of MAPK and EGFR were linked to worse clinical outcomes, including increased lymph node metastasis and reduced patient survival, suggesting these markers could indicate poor prognosis in TNBC cases.

Article Abstract

To investigate the expression and clinical significance of mitogen-activated protein kinase (MAPK) and epidermal growth factor receptor (EGFR) in triple-negative breast cancer (TNBC), a total of 300 TNBC and 120 paired paracancerous tissues were examined. Immunohistochemistry was conducted to determine the expression levels of MAPK and EGFR, and the correlation between MAPK and EGFR expression was evaluated using Cramer's V test. The association between MAPK and EGFR expression, and various clinicopathological variables (such as lymph node metastasis, clinical stage, recurrence and metastasis) was also evaluated, using the χ test. MAPK and EGFR expression levels in TNBC tissues were significantly higher than in the paired paracancerous tissues. Moreover, MAPK expression was associated with that of EGFR in TNBC tissues. The positive expression rates of MAPK and EGFR in patients with lymph node metastasis, advanced clinical stage, tumor recurrence and metastasis were higher than those without. Patients with positive expression of MAPK and EGFR in TNBC tissues had poorer prognoses and lower overall survival times than those without expression. In summary, the expression of MAPK and EGFR is closely associated with tumor invasion and the metastasis of TNBC, and may therefore be used as an indicator of poor prognosis in patients with TNBC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038935PMC
http://dx.doi.org/10.3892/ol.2020.11274DOI Listing

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