Unknown

Dataset Information

0

Sphingolipid metabolism and drug resistance in ovarian cancer.


ABSTRACT: Despite progress in understanding molecular aberrations that contribute to the development and progression of ovarian cancer, virtually all patients succumb to drug resistant disease at relapse. Emerging data implicate bioactive sphingolipids and regulation of sphingolipid metabolism as components of response to chemotherapy or development of resistance. Increases in cytosolic ceramide induce apoptosis in response to therapy with multiple classes of chemotherapeutic agents. Aberrations in sphingolipid metabolism that accelerate the catabolism of ceramide or that prevent the production and accumulation of ceramide contribute to resistance to standard of care platinum- and taxane-based agents. The aim of this review is to highlight current literature and research investigating the influence of the sphingolipids and enzymes that comprise the sphingosine-1-phosphate pathway on the progression of ovarian cancer. The focus of the review is on the utility of sphingolipid-centric therapeutics as a mechanism to circumvent drug resistance in this tumor type.

SUBMITTER: Kreitzburg KM 

PROVIDER: S-EPMC6936734 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

altmetric image

Publications

Sphingolipid metabolism and drug resistance in ovarian cancer.

Kreitzburg Kelly M KM   van Waardenburg Robert C A M RCAM   Yoon Karina J KJ  

Cancer drug resistance (Alhambra, Calif.) 20180919


Despite progress in understanding molecular aberrations that contribute to the development and progression of ovarian cancer, virtually all patients succumb to drug resistant disease at relapse. Emerging data implicate bioactive sphingolipids and regulation of sphingolipid metabolism as components of response to chemotherapy or development of resistance. Increases in cytosolic ceramide induce apoptosis in response to therapy with multiple classes of chemotherapeutic agents. Aberrations in sphing  ...[more]

Similar Datasets

| S-EPMC1422777 | biostudies-other
| S-EPMC5818153 | biostudies-other
| S-EPMC7669681 | biostudies-literature
| S-EPMC8733468 | biostudies-literature
| S-EPMC6460930 | biostudies-literature
| S-EPMC5968444 | biostudies-literature
| S-EPMC5072430 | biostudies-literature
| S-EPMC9104917 | biostudies-literature
| S-EPMC5216767 | biostudies-literature
| S-EPMC4769873 | biostudies-literature