Proteomics advances for precision therapy in ovarian cancer

Marilyne Labrie, Nicholas D. Kendsersky, Hongli Ma, Lydia Campbell, Jennifer Eng, Koei Chin, Gordon B. Mills

Research output: Contribution to journalReview articlepeer-review

5 Scopus citations


Introduction: Due to the relatively low mutation rate and high frequency of copy number variation, finding actionable genetic drivers of high-grade serous carcinoma (HGSC) is a challenging task. Furthermore, emerging studies show that genetic alterations are frequently poorly represented at the protein level adding a layer of complexity. With improvements in large-scale proteomic technologies, proteomics studies have the potential to provide robust analysis of the pathways driving high HGSC behavior. Areas covered: This review summarizes recent large-scale proteomics findings across adequately sized ovarian cancer sample sets. Key words combined with ‘ovarian cancer’ including ‘proteomics’, ‘proteogenomic’, ‘reverse-phase protein array’, ‘mass spectrometry’, and ‘adaptive response’, were used to search PubMed. Expert opinion: Proteomics analysis of HGSC as well as their adaptive responses to therapy can uncover new therapeutic liabilities, which can reduce the emergence of drug resistance and potentially improve patient outcomes. There is a pressing need to better understand how the genomic and epigenomic heterogeneity intrinsic to ovarian cancer is reflected at the protein level and how this information could be used to improve patient outcomes.

Original languageEnglish (US)
Pages (from-to)841-850
Number of pages10
JournalExpert Review of Proteomics
Issue number10
StatePublished - Oct 3 2019


  • Ovarian cancer
  • adaptive responses
  • proteomics

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology


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