Literature DB >> 26206420

An overview of early investigational therapies for chemoresistant ovarian cancer.

Claudia Marchetti1, Jonathan A Ledermann, Pierluigi Benedetti Panici.   

Abstract

INTRODUCTION: Epithelial ovarian cancer (EOC) is the fourth commonest cause of female cancer death in the developed world. Although progress in treatment has improved survival, ∼ 80% of patients with advanced EOC will experience a recurrence and eventually will become resistant to chemotherapy. The aim of treatment for chemoresistant EOC has traditionally been limited to palliation of symptoms but the recent introduction of new therapies targeting molecular pathways is beginning to demonstrate improvements in disease control. AREAS COVERED: This review provides an overview of early investigational drugs for the treatment of 'platinum-resistant' EOC. The article is based on English peer-reviewed articles located on MEDLINE and related abstracts presented at major international meetings. EXPERT OPINION: Drugs targeting several pathways are increasingly used to treat 'platinum-resistant' EOC. Currently, drugs targeting the angiogenesis pathway have been shown to significantly improve patient outcome. Studies are also being undertaken with inhibitors of poly(ADP-ribose) polymerase (PARP), targeting the DNA repair pathway as it is possible that the benefits seen with these agents in 'platinum-sensitive' disease will apply to those with 'platinum-resistant' disease. The discovery of predictive biomarkers that identify patients which benefit from these targeted therapies is paramount to the success of these treatments in the future.

Entities:  

Keywords:  angiogenesis; chemotherapy; immune checkpoint inhibitors; ovarian cancer; recurrence; resistant; targeted therapy

Mesh:

Substances:

Year:  2015        PMID: 26206420     DOI: 10.1517/13543784.2015.1072168

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  6 in total

1.  Hyaluronic acid conjugated nanoparticle delivery of siRNA against TWIST reduces tumor burden and enhances sensitivity to cisplatin in ovarian cancer.

Authors:  Sophia A Shahin; Ruining Wang; Shirleen I Simargi; Altagracia Contreras; Liliana Parra Echavarria; Louise Qu; Wei Wen; Thanh Dellinger; Juli Unternaehrer; Fuyuhiko Tamanoi; Jeffrey I Zink; Carlotta A Glackin
Journal:  Nanomedicine       Date:  2018-04-14       Impact factor: 5.307

2.  New perspective on maintenance therapies for platinum- sensitive recurrent ovarian cancer in women with germline and somatic mutations in BRCA1 and BRCA2 genes.

Authors:  I Vergote; V Bours; B Blaumeiser; J-F Baurain
Journal:  Facts Views Vis Obgyn       Date:  2016-09

3.  Targeting estrogen receptor beta (ERβ) for treatment of ovarian cancer: importance of KDM6B and SIRT1 for ERβ expression and functionality.

Authors:  Giulia Pinton; Stefan Nilsson; Laura Moro
Journal:  Oncogenesis       Date:  2018-02-09       Impact factor: 7.485

4.  Role of Wnt/β-catenin, Wnt/c-Jun N-terminal kinase and Wnt/Ca2+ pathways in cisplatin-induced chemoresistance in ovarian cancer.

Authors:  Lu Huang; Ye Jin; Shujun Feng; Yuqing Zou; Sainan Xu; Shuang Qiu; Ling Li; Jianhua Zheng
Journal:  Exp Ther Med       Date:  2016-11-08       Impact factor: 2.447

5.  Therapeutic Targeting of Ovarian Cancer Stem Cells Using Estrogen Receptor Beta Agonist.

Authors:  Yi He; Salvador Alejo; Prabhakar Pitta Venkata; Jessica D Johnson; Ilanna Loeffel; Uday P Pratap; Yi Zou; Zhao Lai; Rajeshwar R Tekmal; Edward R Kost; Gangadhara R Sareddy
Journal:  Int J Mol Sci       Date:  2022-06-28       Impact factor: 6.208

6.  Sialyltransferase ST3GAL1 promotes cell migration, invasion, and TGF-β1-induced EMT and confers paclitaxel resistance in ovarian cancer.

Authors:  Xin Wu; Junda Zhao; Yuanyuan Ruan; Li Sun; Congjian Xu; Hua Jiang
Journal:  Cell Death Dis       Date:  2018-10-30       Impact factor: 8.469

  6 in total

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