Evidence map›Paper›PMID 34066486›Full record

ReviewCancers2021

PBK/TOPK: An Effective Drug Target with Diverse Therapeutic Potential.

Hai Huang, Mee-Hyun Lee, Kangdong Liu, Zigang Dong, Zeayoung Ryoo, Myoung Ok Kim

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. TOPK Suppresses the CD8Cancer communications (London, England) · 2026
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
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  19. The role ofHeliyon · 2024
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Hai HuangDepartment of Animal Science and Biotechnology, ITRD, Kyungpook National University, Sangju 37224, Korea.
Mee-Hyun LeeCollege of Korean Medicine, Dongshin University, Naju, Jeollanamdo 58245, Korea.
Kangdong LiuChina-US (Henan) Hormel Cancer Institute, Zhengzhou 450008, China.ORCID 0000-0002-4425-5625
Zigang DongChina-US (Henan) Hormel Cancer Institute, Zhengzhou 450008, China.ORCID 0000-0002-4174-4028
Zeayoung RyooSchool of Life Science, Kyungpook National University, Daegu 41566, Korea.
Myoung Ok KimDepartment of Animal Science and Biotechnology, ITRD, Kyungpook National University, Sangju 37224, Korea.
Kyungpook National University · KRZhengzhou University · CNDongshin University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-lymphokine-activated killer cell-originated protein kinase (TOPK, also known as PDZ-binding kinase or PBK) plays a crucial role in cell cycle regulation and mitotic progression. Abnormal overexpression or activation of TOPK has been observed in many cancers, including colorectal cancer, triple-negative breast cancer, and melanoma, and it is associated with increased development, dissemination, and poor clinical outcomes and prognosis in cancer. Moreover, TOPK phosphorylates p38, JNK, ERK, and AKT, which are involved in many cellular functions, and participates in the activation of multiple signaling pathways related to MAPK, PI3K/PTEN/AKT, and NOTCH1; thus, the direct or indirect interactions of TOPK make it a highly attractive yet elusive target for cancer therapy. Small molecule inhibitors targeting TOPK have shown great therapeutic potential in the treatment of cancer both in vitro and in vivo, even in combination with chemotherapy or radiotherapy. Therefore, targeting TOPK could be an important approach for cancer prevention and therapy. Thus, the purpose of the present review was to consider and analyze the role of TOPK as a drug target in cancer therapy and describe the recent findings related to its role in tumor development. Moreover, this review provides an overview of the current progress in the discovery and development of TOPK inhibitors, considering future clinical applications.

Indexed as

cancer therapyinhibitorssignaling pathwayTOPK

Identifiers

PMID34066486
PMCPMC8124186
OpenAlexW3159224581

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.