4.5 Article

PLK1 inhibition-based combination therapies for cancer management

Journal

TRANSLATIONAL ONCOLOGY
Volume 16, Issue -, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.tranon.2021.101332

Keywords

PLK1; Cancer; Combination therapies; Targeted therapy; Immunotherapy

Categories

Funding

  1. NIH [R01 AR059130, P30 CA014520]
  2. Department of Veterans Affairs (VA) [I01 CX001441, I01 BX004221, IK6 BX003780]

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This review discusses the role of PLK1 in cancer and the advantages of combining PLK1 inhibitors with other drugs for cancer treatment. PLK1 inhibitors in combination with chemotherapy drugs and targeted small molecules have shown superior effects against cancer both in vitro and in vivo. However, further research is needed to identify the best combination targets and drug combinations.
Polo-like kinase I (PLK1), a cell cycle regulating kinase, has been shown to have oncogenic function in several cancers. Although PLK1 inhibitors, such as BI2536, BI6727 (volasertib) and NMS-1286937 (onvansertib) are generally well-tolerated with a favorable pharmacokinetic profile, clinical successes are limited due to partial responses in cancer patients, especially those in advanced stages. Recently, combination therapies targeting multiple pathways are being tested for cancer management. In this review, we first discuss structure and function of PLK1, role of PLK1 in cancers, PLK1 specific inhibitors, and advantages of using combination therapy versus monotherapy followed by a critical account on PLK1-based combination therapies in cancer treatments, especially highlighting recent advancements and challenges. PLK1 inhibitors in combination with chemotherapy drugs and targeted small molecules have shown superior effects against cancer both in vitro and in vivo. PLK1-based combination therapies have shown increased apoptosis, disrupted cell cycle, and potential to overcome resistance in cancer cells/tissues over monotherapies. Further, with successes in preclinical experiments, researchers are validating such approaches in clinical trials. Although PLK1-based combination therapies have achieved initial success in clinical studies, there are examples where they have failed to improve patient survival. Therefore, further research is needed to identify and validate novel biologically informed co-targets for PLK1based combinatorial therapies. Employing a network-based analysis, we identified potential PLK1 co-targets that could be examined further. In addition, understanding the mechanisms of synergism between PLK1 inhibitors and other agents may lead to a better approach on which agents to pair with PLK1 inhibition for optimum cancer treatment.

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