HER-2 and NF-κB as the targets for therapy-resistant breast cancer

Kazi M. Ahmed, Ning Cao, Jian-Jian Li

Research output: Contribution to journalArticle

51 Scopus citations

Abstract

HER-2 (also called ErbB2 or Neu) tyrosine kinase, one of the four members of ErbB receptor family (ErbB1, i.e., EGFR, ErbB2, ErbB3 and ErbB4), plays a critical role in the control of diverse cellular functions involved in differentiation, proliferation, migration and cell survival via multiple signal transduction pathways. Overexpression of HER-2, observed in HER-2-positive breast cancer patients, is believed to cause the tumor resistance to an array of anti-cancer agents and poor prognosis. Although HER-2 antibodies have shown growth inhibitory effects, more efficient molecular targets against HER-2-mediated tumor resistance need to be developed. The molecular mechanisms underlying HER-2-mediated tumor resistance, especially the connections between HER-2 and therapy-resistant signaling networks, need to be further investigated. NF-KB, a key stress transcription factor that can initiate a pro-survival network, was found to be activated in many cancer cells overexpressing HER-2 and to be responsible for the radiation resistance in HER-2 transfected breast cancer cells. Recent findings in literature and data from this laboratory suggest a possible co-operation between HER-2 and NF-κB in signaling tumor resistance to radiotherapy. This review will discuss the mechanisms of HER-2 mediated NF-κB signaling pathway and potential target for therapeutic intervention.

Original languageEnglish (US)
Pages (from-to)4235-4243
Number of pages9
JournalAnticancer Research
Volume26
Issue number6 B
StatePublished - Nov 2006
Externally publishedYes

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Keywords

  • Drug resistance
  • HER-2
  • Herceptin
  • NF-κB
  • Radiotherapy resistance
  • Review

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

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