Unknown

Dataset Information

0

Current progress and future perspectives in the development of anti-polo-like kinase 1 therapeutic agents.


ABSTRACT: Although significant levels of side effects are often associated with their use, microtubule-directed agents that primarily target fast-growing mitotic cells have been considered to be some of the most effective anti-cancer therapeutics. With the hope of developing new-generation anti-mitotic agents with reduced side effects and enhanced tumor specificity, researchers have targeted various proteins whose functions are critically required for mitotic progression. As one of the highly attractive mitotic targets, polo-like kinase 1 (Plk1) has been the subject of an extensive effort for anti-cancer drug discovery. To date, a variety of anti-Plk1 agents have been developed, and several of them are presently in clinical trials. Here, we will discuss the current status of generating anti-Plk1 agents as well as future strategies for designing and developing more efficacious anti-Plk1 therapeutics.

SUBMITTER: Park JE 

PROVIDER: S-EPMC5497816 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

altmetric image

Publications

Current progress and future perspectives in the development of anti-polo-like kinase 1 therapeutic agents.

Park Jung-Eun JE   Hymel David D   Burke Terrence R TR   Lee Kyung S KS  

F1000Research 20170629


Although significant levels of side effects are often associated with their use, microtubule-directed agents that primarily target fast-growing mitotic cells have been considered to be some of the most effective anti-cancer therapeutics. With the hope of developing new-generation anti-mitotic agents with reduced side effects and enhanced tumor specificity, researchers have targeted various proteins whose functions are critically required for mitotic progression. As one of the highly attractive m  ...[more]

Similar Datasets

| S-EPMC2819039 | biostudies-other
2019-08-10 | GSE135618 | GEO
| S-EPMC7132033 | biostudies-literature
| S-EPMC8038573 | biostudies-literature
| S-EPMC8670224 | biostudies-literature
| S-EPMC7407196 | biostudies-literature
| S-EPMC6789600 | biostudies-literature
| S-EPMC7366992 | biostudies-literature
| S-EPMC5337853 | biostudies-literature
| S-EPMC4061466 | biostudies-literature