Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 May;34(5):2069-77.

Advanced epithelial ovarian cancer: from standard chemotherapy to promising molecular pathway targets--where are we now?

Affiliations
  • PMID: 24778008
Review

Advanced epithelial ovarian cancer: from standard chemotherapy to promising molecular pathway targets--where are we now?

John Syrios et al. Anticancer Res. 2014 May.

Abstract

Ovarian cancer is the most frequent cause of death from gynaecological malignancy in the Western countries, and differences in outcome among different histological subtypes are being increasingly recognized. It is generally considered as chemosensitive, but resistant clones evolve in the majority of cases, at varying rates. In this brief review, we describe advances in conventional chemotherapy, particularly the use of weekly paclitaxel. We then focus on new promising agents that target certain pathways which drive the genesis and evolution of ovarian cancer; these include poly(ADP-ribose) polymerase (PARP) inhibitors targeting tumor cells deficient in homologous recombination. We also discuss other targets including the folate receptor. Ovarian cancer has also proved to be one of the most sensitive types of cancer to an anti-angiogenic approach and we summarize recent experience using a range of agents.

Keywords: Conventional chemotherapy; PARP inhibitors; epithelial ovarian cancer; histological subtypes; molecular pathway targets; review; tumour angiogenesis; tyrosine kinase inhibitors.

PubMed Disclaimer

Publication types

MeSH terms

Substances

LinkOut - more resources