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Overexpression of sonic hedgehog in the triple negative breast cancer: Clinicopathological characteristics of high burden breast cancer patients from Bangladesh

  • A. S. Noman
  • , M. Uddin
  • , M. Z. Rahman
  • , M. J. Nayeem
  • , S. S. Alam
  • , Z. Khatun
  • , M. Wahiduzzaman
  • , A. Sultana
  • , M. L. Rahman
  • , M. Y. Ali
  • , D. Barua
  • , I. Ahmed
  • , M. S. Islam
  • , A. Aboussekhra
  • , H. Yeger
  • , W. A. Farhat
  • , S. S. Islam
  • University of Chittagong
  • University of Toronto
  • Chittagong Medical College Hospital
  • King Faisal Specialist Hospital and Research Centre

Producción científica › revisión exhaustiva

56 Citas (Scopus)

Resumen

Dysregulation of Hedgehog (Hh) signaling pathway has been documented in mammary gland development and breast cancer (BC) progression. Despite the remarkable progress in therapeutic interventions, BC related mortality in Bangladesh increased in the last decade. Triple negative breast cancer (TNBC) still presents a critical therapeutic challenge. Thus effective targeted therapy is urgently needed. In this study, we report the clinicopathological characteristics and prognosis of BC patients from Bangladesh. Routine immunohistochemical analysis and high throughput RNA-Seq data from the TCGA library were used to analyze the expression pattern and association of high and low level of Shh expression in a collection of BC patients with a long-term follow-up. High levels of Shh were observed in a subset of BC tumors with poor prognostic pathological features. Higher level of Shh expression correlated with a significantly poorer overall survival of patients compared with patients whose tumors expressed a low level of Shh. These data support the contention that Shh could be a novel biomarker for breast cancer that is involved in mediating the aggressive phenotype of BC. We propose that BC patients exhibiting a higher level of Shh expression, representing a subset of BC patients, would be amenable to Shh targeted therapy.

Idioma originalEnglish
Número de artículo18830
PublicaciónScientific Reports
Volumen6
DOI
EstadoPublished - 5 ene 2016
Publicado de forma externaSí

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